Our client is on the hunt for a talented and experienced Lab Director to work with their team in Pennsylvania. As laboratory director, you are responsible for the overall operation and administration of the laboratory, including the employment of competent qualified personnel. You remain ultimately responsible for the Laboratory and must ensure that all the duties are properly performed and compliance/regulations are met. Responsibilities: Supervision of all testing personnel and reporting of test results as well as provide on-site supervision for specific minimally qualified testing personnel when they are performing high complexity testing. Managing a team of 10+ employees Ensure operations comply with all regulations, policies, and procedures relating to safety, security, and health. Responsible for the overall operation and administration of the laboratory, including the employment of personnel who are competent to perform test procedures, record and report test results promptly, accurately and proficiently, and for assuring compliance with the applicable regulations. Work directly with Chief Science Officer and Executive team as needed Managing the lab and also identifying and implementing the appropriate strategies for reducing costs and improving the quality of services. Requirements: Masters Degree or PHD in Chemistry or related field Minimum of 5 years' experience in a pharmaceutical or related laboratory setting Must have experience managing and leading a team Experience with HPLC, UPLC, GCMS, ICP/MS techniques and instruments
Feb 17, 2020
Full time
Our client is on the hunt for a talented and experienced Lab Director to work with their team in Pennsylvania. As laboratory director, you are responsible for the overall operation and administration of the laboratory, including the employment of competent qualified personnel. You remain ultimately responsible for the Laboratory and must ensure that all the duties are properly performed and compliance/regulations are met. Responsibilities: Supervision of all testing personnel and reporting of test results as well as provide on-site supervision for specific minimally qualified testing personnel when they are performing high complexity testing. Managing a team of 10+ employees Ensure operations comply with all regulations, policies, and procedures relating to safety, security, and health. Responsible for the overall operation and administration of the laboratory, including the employment of personnel who are competent to perform test procedures, record and report test results promptly, accurately and proficiently, and for assuring compliance with the applicable regulations. Work directly with Chief Science Officer and Executive team as needed Managing the lab and also identifying and implementing the appropriate strategies for reducing costs and improving the quality of services. Requirements: Masters Degree or PHD in Chemistry or related field Minimum of 5 years' experience in a pharmaceutical or related laboratory setting Must have experience managing and leading a team Experience with HPLC, UPLC, GCMS, ICP/MS techniques and instruments
Company Overview BioHybrid Solutions LLC is a Carnegie Mellon University spin-off. Our mission is to revolutionize the use of proteins across a wide variety of industries through our polymer-based protein-engineering platform. We are focused on opportunities in biocatalysis, therapeutics, diagnostics, and devices. We are looking for ambitious and motivated candidates who are excited to work in a fast-paced startup environment. Job Summary BioHybrid Solutions is seeking an expert in analytical characterization methods focused on size evaluation of proteins, polymers and protein-polymer conjugates. The successful candidate will be working in a team focused on the development and characterization of protein-based materials for various industrial applications. You will be responsible for planning and conducting research aimed to deliver advanced novel products or providing research support for existing products by leveraging protein-polymer synthesis and characterization. This position requires a strong background in analytical chemistry. Daily activities will involve lab work, preparation of reports and technical presentations. Experience and Education PhD degree with 0-5 years of experience or B.S./M.S. with 5+ years of experience in related disciplines. Desirable Skills and Knowledge Broad training in protein and/or polymer characterization including: proficiency in chromatographic methods and instrumentation such as: Gel permeation chromotography (GPC) / Size exclusion chromotography (SEC) Static light scattering methods (dual angle, multi-angle - MALLS) Field-flow fractionation method Strong background in laboratory work and skills Strong reporting/analytical skills Strong verbal and written communications skills Ability to work within a diverse work team Candidates must be authorized to work in US. Application Process Apply with your resume and cover letter at BioHybrid Solutions provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws.
Feb 17, 2020
Full time
Company Overview BioHybrid Solutions LLC is a Carnegie Mellon University spin-off. Our mission is to revolutionize the use of proteins across a wide variety of industries through our polymer-based protein-engineering platform. We are focused on opportunities in biocatalysis, therapeutics, diagnostics, and devices. We are looking for ambitious and motivated candidates who are excited to work in a fast-paced startup environment. Job Summary BioHybrid Solutions is seeking an expert in analytical characterization methods focused on size evaluation of proteins, polymers and protein-polymer conjugates. The successful candidate will be working in a team focused on the development and characterization of protein-based materials for various industrial applications. You will be responsible for planning and conducting research aimed to deliver advanced novel products or providing research support for existing products by leveraging protein-polymer synthesis and characterization. This position requires a strong background in analytical chemistry. Daily activities will involve lab work, preparation of reports and technical presentations. Experience and Education PhD degree with 0-5 years of experience or B.S./M.S. with 5+ years of experience in related disciplines. Desirable Skills and Knowledge Broad training in protein and/or polymer characterization including: proficiency in chromatographic methods and instrumentation such as: Gel permeation chromotography (GPC) / Size exclusion chromotography (SEC) Static light scattering methods (dual angle, multi-angle - MALLS) Field-flow fractionation method Strong background in laboratory work and skills Strong reporting/analytical skills Strong verbal and written communications skills Ability to work within a diverse work team Candidates must be authorized to work in US. Application Process Apply with your resume and cover letter at BioHybrid Solutions provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws.
With operations in 35+ nations and ~ 20,000 employees worldwide, CSL is driven to develop and deliver a broad range of lifesaving therapies to treat disorders such as hemophilia and primary immune deficiencies, and vaccines to prevent influenza. Our therapies are also used in cardiac surgery, organ transplantation and burn treatment. CSL is the parent company of CSL Behring and Seqirus. CSL Behring is a global leader in the protein biotherapeutics industry, focused on bringing to market biotherapies used to treat serious and often rare conditions. CSL Behring operates CSL Plasma, one of the world's largest collectors of human plasma, which is used to create CSL's therapies. Seqirus is the second largest influenza vaccine company in the world and is a transcontinental partner in pandemic preparedness and a major contributor to the prevention and control of influenza globally. We invite you to take a look at the many career possibilities available around the globe and consider building your promising future at CSL by becoming a member of our team! Responsibilities The Clinical Pharmacology and Pharmacometrics team of CSL Behring is seeking a Senior Pharmacometrician/AD Pharmacometrics responsible for activities within specific projects at the pre-clinical stage as well as those across all clinical stages at CSL. This role will contribute to the pharmacometric strategy for projects, regulatory submissions, or interactions with authorities, working in parallel to Clinical Pharmacologists, Clinical Program Directors, and other experienced Clinical Development Team (CDT) colleagues, at a project level to align and set pharmacometrics strategy. This role will also assist in interactions with external consultants or with academic institutions. There is a degree of flexibility with regards to level (see qualifications/experience section below)--depending upon experience, this role can be filled at the Pharmacometrician, Senior Pharmacometrician or Associate Director level. At the Associate Director level, the individual assuming this role will have a strong and proven pharmacokinetic/pharmacometrics knowledge, with demonstrable modelling and simulation skills, and will work in close collaboration with various non-clinical, Research, Clinical R&D, & Commercial Development/Medical Affairs functions. The role will work significantly independently, requiring minimal technical management or guidance. A considerable amount of initiative and strategic thinking will also be expected. This role may also be able to supervise more junior-level Pharmacometricians who will be serving at a project and/or a study level and will also assist in interactions with senior-level external consultants or with academic institutions. Qualifications Responsibilities Lead the implementation of model-based drug development strategies for assigned preclinical, clinical, and lifecycle management projects Manage all necessary hardware and software systems, together with relevant quality processes, for the conduct of in-house pharmacometrics activities. Execute relevant pharmacometric analyses for assigned preclinical, clinical, and lifecycle management projects: non-compartmental PK, PK/PD analyses, population PK and PK/PD, clinical trial simulations, meta-analyses, disease and systems biology modelling, and other modeling and simulation activities as appropriate for the project. Apply innovative analytical methods in pharmacometrics/modelling and simulation to integrate knowledge of pharmacokinetics, pharmacodynamics, patient characteristics and disease states in support of optimal study designs Provide pharmacometrics contributions to regulatory documents including Investigator Brochures, Labelling and those required for regulatory meetings and regulatory filings. Provides resolution of pharmacometrics queries from regulatory agencies, taking a lead role in writing and reviewing responses to regulatory queries Write Modeling & Simulation Analysis Plans and Reports. Provides input for, or leads derivation of, standard operation procedures and best practices in pharmacometrics for the Early Development function Provide technical support to Research in the development of preclinical PK/PD model required for early clinical development strategy, as well as utilizing Pharm-Tox data appropriately to make clinical dosing decisions. Analyze and interpret all study PK, PK/PD and pharmacometric outcomes. Ability to create PK/PD files according to standard specifications and to generate tables and listings as required Develop external alliances with consultants, contract organizations and academic institutions to ensure timely conduct of all pharmacometrics deliverables for projects, to continually keep abreast of the science, as well as development of more junior colleagues in the discipline Input to licensing projects as needed Associate Directors will act as a mentor to junior pharmacometricians, providing strategic and technical guidance for their activities. Capabilities Education: Doctoral degree with demonstrated expertise in pharmacometrics and strong quantitative skills (eg proven experience in most of the following areas: population and PK/PD modelling, mechanistic modelling, systems biology, species scaling methodologies and derivation of first-in-human doses, disease modelling and meta-analyses). Experience: Associate Director: A minimum of 5 years of pharmaceutical industry (or relevant) experience,specifically contributing to pharmacometrics aspects of clinical drug development. Senior Pharmacometrician: A minimum of 3 years, specifically contributing to pharmacometrics aspects of clinical drug development. Pharmacometrician: A minimum of 1 year experience of pharmaceutical industry (or relevant) experience, specifically contributing to the pharmacometrics aspects of clinical drug development. For all levels: In-depth knowledge and experience in advanced PK and PK/PD Advanced pharmacometric knowledge in one of the following core sub-speciality: Systems Pharmacology, advanced Exposure-Response Models, Disease Models, Physiological-Based Pharmacokinetic Models Advanced knowledge and experience of software such as NONMEM, SAS, S-Plus, R, WinNonlin, and other server-based data processing and modelling tools Knowledge of the role of pharmacometrics in drug development and FDA/ICH requirements for drug registration Knowledge and application of statistics, random effects modelling, mixed effects modelling, data mining, population PK/PD analyses and modelling (including nonlinear models), Bayesian methods, clinical utility indices, and Monte-Carlo simulation, and clinical trial design and simulation Ability to understand, lead and implement all aspects of pharmacometrics needs across a variety of disease areas Competencies: Excellent skills in the use of NONMEM, PsN, R, and Phoenix. Excellent communication skills with demonstrated ability to effectively present any aspect of this highly technical field, as well as its plans/strategies, accordingly to various audiences in both verbal and written form. Excellent oral presentation skills. Ability to independently lead, conduct, and communicate pharmacometrics plans/strategies and analyses. Ability to create publications according to international scientific standards. Good interpersonal skills, including a positive and constructive attitude and ability to effectively work in a team Matrix environment. Negotiation and influential skills advantageous. Ability to work collaboratively within a matrixed organization. Worker Type: Employee Worker Sub Type: Regular
Feb 17, 2020
Full time
With operations in 35+ nations and ~ 20,000 employees worldwide, CSL is driven to develop and deliver a broad range of lifesaving therapies to treat disorders such as hemophilia and primary immune deficiencies, and vaccines to prevent influenza. Our therapies are also used in cardiac surgery, organ transplantation and burn treatment. CSL is the parent company of CSL Behring and Seqirus. CSL Behring is a global leader in the protein biotherapeutics industry, focused on bringing to market biotherapies used to treat serious and often rare conditions. CSL Behring operates CSL Plasma, one of the world's largest collectors of human plasma, which is used to create CSL's therapies. Seqirus is the second largest influenza vaccine company in the world and is a transcontinental partner in pandemic preparedness and a major contributor to the prevention and control of influenza globally. We invite you to take a look at the many career possibilities available around the globe and consider building your promising future at CSL by becoming a member of our team! Responsibilities The Clinical Pharmacology and Pharmacometrics team of CSL Behring is seeking a Senior Pharmacometrician/AD Pharmacometrics responsible for activities within specific projects at the pre-clinical stage as well as those across all clinical stages at CSL. This role will contribute to the pharmacometric strategy for projects, regulatory submissions, or interactions with authorities, working in parallel to Clinical Pharmacologists, Clinical Program Directors, and other experienced Clinical Development Team (CDT) colleagues, at a project level to align and set pharmacometrics strategy. This role will also assist in interactions with external consultants or with academic institutions. There is a degree of flexibility with regards to level (see qualifications/experience section below)--depending upon experience, this role can be filled at the Pharmacometrician, Senior Pharmacometrician or Associate Director level. At the Associate Director level, the individual assuming this role will have a strong and proven pharmacokinetic/pharmacometrics knowledge, with demonstrable modelling and simulation skills, and will work in close collaboration with various non-clinical, Research, Clinical R&D, & Commercial Development/Medical Affairs functions. The role will work significantly independently, requiring minimal technical management or guidance. A considerable amount of initiative and strategic thinking will also be expected. This role may also be able to supervise more junior-level Pharmacometricians who will be serving at a project and/or a study level and will also assist in interactions with senior-level external consultants or with academic institutions. Qualifications Responsibilities Lead the implementation of model-based drug development strategies for assigned preclinical, clinical, and lifecycle management projects Manage all necessary hardware and software systems, together with relevant quality processes, for the conduct of in-house pharmacometrics activities. Execute relevant pharmacometric analyses for assigned preclinical, clinical, and lifecycle management projects: non-compartmental PK, PK/PD analyses, population PK and PK/PD, clinical trial simulations, meta-analyses, disease and systems biology modelling, and other modeling and simulation activities as appropriate for the project. Apply innovative analytical methods in pharmacometrics/modelling and simulation to integrate knowledge of pharmacokinetics, pharmacodynamics, patient characteristics and disease states in support of optimal study designs Provide pharmacometrics contributions to regulatory documents including Investigator Brochures, Labelling and those required for regulatory meetings and regulatory filings. Provides resolution of pharmacometrics queries from regulatory agencies, taking a lead role in writing and reviewing responses to regulatory queries Write Modeling & Simulation Analysis Plans and Reports. Provides input for, or leads derivation of, standard operation procedures and best practices in pharmacometrics for the Early Development function Provide technical support to Research in the development of preclinical PK/PD model required for early clinical development strategy, as well as utilizing Pharm-Tox data appropriately to make clinical dosing decisions. Analyze and interpret all study PK, PK/PD and pharmacometric outcomes. Ability to create PK/PD files according to standard specifications and to generate tables and listings as required Develop external alliances with consultants, contract organizations and academic institutions to ensure timely conduct of all pharmacometrics deliverables for projects, to continually keep abreast of the science, as well as development of more junior colleagues in the discipline Input to licensing projects as needed Associate Directors will act as a mentor to junior pharmacometricians, providing strategic and technical guidance for their activities. Capabilities Education: Doctoral degree with demonstrated expertise in pharmacometrics and strong quantitative skills (eg proven experience in most of the following areas: population and PK/PD modelling, mechanistic modelling, systems biology, species scaling methodologies and derivation of first-in-human doses, disease modelling and meta-analyses). Experience: Associate Director: A minimum of 5 years of pharmaceutical industry (or relevant) experience,specifically contributing to pharmacometrics aspects of clinical drug development. Senior Pharmacometrician: A minimum of 3 years, specifically contributing to pharmacometrics aspects of clinical drug development. Pharmacometrician: A minimum of 1 year experience of pharmaceutical industry (or relevant) experience, specifically contributing to the pharmacometrics aspects of clinical drug development. For all levels: In-depth knowledge and experience in advanced PK and PK/PD Advanced pharmacometric knowledge in one of the following core sub-speciality: Systems Pharmacology, advanced Exposure-Response Models, Disease Models, Physiological-Based Pharmacokinetic Models Advanced knowledge and experience of software such as NONMEM, SAS, S-Plus, R, WinNonlin, and other server-based data processing and modelling tools Knowledge of the role of pharmacometrics in drug development and FDA/ICH requirements for drug registration Knowledge and application of statistics, random effects modelling, mixed effects modelling, data mining, population PK/PD analyses and modelling (including nonlinear models), Bayesian methods, clinical utility indices, and Monte-Carlo simulation, and clinical trial design and simulation Ability to understand, lead and implement all aspects of pharmacometrics needs across a variety of disease areas Competencies: Excellent skills in the use of NONMEM, PsN, R, and Phoenix. Excellent communication skills with demonstrated ability to effectively present any aspect of this highly technical field, as well as its plans/strategies, accordingly to various audiences in both verbal and written form. Excellent oral presentation skills. Ability to independently lead, conduct, and communicate pharmacometrics plans/strategies and analyses. Ability to create publications according to international scientific standards. Good interpersonal skills, including a positive and constructive attitude and ability to effectively work in a team Matrix environment. Negotiation and influential skills advantageous. Ability to work collaboratively within a matrixed organization. Worker Type: Employee Worker Sub Type: Regular
Civil & Environmental Consultants (CEC)
Langhorne, PA, USA
Overview As a Geologist/Environmental Scientist for Civil & Environmental Consultants, Inc. (CEC), you'll be directly involved with environmental compliance monitoring and assessment projects. Your primary responsibility will be completing field activities, including: assisting with and leading field sampling activities for groundwater, surface water, sediment, air and soil monitoring/assessment projects; monitoring soil boring installation and bedrock coring activities; field screening of various media for evidence of environmental impacts; documenting groundwater monitoring well and piezometer installation activities. You will also assist with reporting activities, including managing and interpreting environmental data, developing potentiometric surface maps and geologic cross sections, and report development. The individual's degree of involvement will be based upon his/her exposure and experience with respect to the assigned work. Role and responsibilities: Collect, analyze, and prepare raw data into workable form for engineering/scientific project reports, plans, specifications, permits, cost estimates, and other project documents. Participate in field work as necessary/required in order to accomplish tasks assigned by project team leadership. Help to coordinate assigned tasks with staff to successfully complete discreet tasks as assigned on projects. Report progress to team leadership. Maintain and utilize working knowledge of accepted engineering design, scientific principles, regulatory programs, and field standards and practices in the execution of design work as directed by supervisor and conform to industry standards. Provide input and assistance in investigating new techniques and methods that may increase the Company's efficiency and incorporate cutting-edge applications to arrive at the desired result on projects. Qualifications The qualified candidate will have approximately 2-5 years of professional experience with a degree in Environmental Science, Geology, or Environmental Engineering (or equivalent), have a valid driver's license and access to a vehicle, and have current 40-hour Hazwoper training. Basic technical competency, and demonstrated skills in engineering/scientific judgment, mathematical-applications, verbal/written communications; Ability to work effectively with team members as well as independently; Strong quantitative/math and analytical skills; The ability to participate in field work and or attend client meetings; Experience with field sampling in NJ, NJDEP Technical Requirements for Site Remediation Core competency in Microsoft Office Products, including Word, Excel, PowerPoint, and Outlook; Detailed Oriented with excellent oral and written communication skills; and, As required by discipline, take training courses/secure certifications in various specialized areas such as health and safety, hazardous materials inspection (asbestos, lead, etc.), wetland delineation and/or natural resource inventories, sample collection techniques, environmental site assessments, etc. About Us CEC offers big firm opportunities with a small firm culture . We understand the importance of professional growth and offer career advancement and leadership opportunities. You will work on diverse projects providing high quality services to our clients. Join our team where your contribution matters.
Feb 17, 2020
Full time
Overview As a Geologist/Environmental Scientist for Civil & Environmental Consultants, Inc. (CEC), you'll be directly involved with environmental compliance monitoring and assessment projects. Your primary responsibility will be completing field activities, including: assisting with and leading field sampling activities for groundwater, surface water, sediment, air and soil monitoring/assessment projects; monitoring soil boring installation and bedrock coring activities; field screening of various media for evidence of environmental impacts; documenting groundwater monitoring well and piezometer installation activities. You will also assist with reporting activities, including managing and interpreting environmental data, developing potentiometric surface maps and geologic cross sections, and report development. The individual's degree of involvement will be based upon his/her exposure and experience with respect to the assigned work. Role and responsibilities: Collect, analyze, and prepare raw data into workable form for engineering/scientific project reports, plans, specifications, permits, cost estimates, and other project documents. Participate in field work as necessary/required in order to accomplish tasks assigned by project team leadership. Help to coordinate assigned tasks with staff to successfully complete discreet tasks as assigned on projects. Report progress to team leadership. Maintain and utilize working knowledge of accepted engineering design, scientific principles, regulatory programs, and field standards and practices in the execution of design work as directed by supervisor and conform to industry standards. Provide input and assistance in investigating new techniques and methods that may increase the Company's efficiency and incorporate cutting-edge applications to arrive at the desired result on projects. Qualifications The qualified candidate will have approximately 2-5 years of professional experience with a degree in Environmental Science, Geology, or Environmental Engineering (or equivalent), have a valid driver's license and access to a vehicle, and have current 40-hour Hazwoper training. Basic technical competency, and demonstrated skills in engineering/scientific judgment, mathematical-applications, verbal/written communications; Ability to work effectively with team members as well as independently; Strong quantitative/math and analytical skills; The ability to participate in field work and or attend client meetings; Experience with field sampling in NJ, NJDEP Technical Requirements for Site Remediation Core competency in Microsoft Office Products, including Word, Excel, PowerPoint, and Outlook; Detailed Oriented with excellent oral and written communication skills; and, As required by discipline, take training courses/secure certifications in various specialized areas such as health and safety, hazardous materials inspection (asbestos, lead, etc.), wetland delineation and/or natural resource inventories, sample collection techniques, environmental site assessments, etc. About Us CEC offers big firm opportunities with a small firm culture . We understand the importance of professional growth and offer career advancement and leadership opportunities. You will work on diverse projects providing high quality services to our clients. Join our team where your contribution matters.
Civil & Environmental Consultants (CEC)
Pitcairn, PA, USA
Overview As an Air Quality Scientist / Engineer for Civil & Environmental Consultants, Inc. (CEC), you will evaluate and present information regarding atmospheric emissions from proposed processes and equipment in support of state and federal permit applications. Job duties will include performing engineering calculations, compiling permit application documents, meeting and coordinating with clients to obtain and understand project information, communicating with agency personnel, and evaluating control technologies for client facilities. Qualifications BS or MS in Environmental Engineering, Chemical Engineering, Environmental Sciences, Meteorology, or related fields; Experience with atmospheric emission inventory calculations, air permit application preparation, and pollution control technologies; and Excellent written and verbal communication skills; 8+ years consulting, compliance, or industry experience; Knowledge of PA, OH, WV Regulations, and USEPA air quality regulations; Knowledge of New Source Review procedures; Familiarity with air compliance needs of the natural gas, manufacturing, or power industries; and Strong experience with air permitting and compliance for the oil and gas industry. About Us CEC offers big firm opportunities with a small firm culture. We understand the importance of professional growth and offer career advancement and leadership opportunities. You will work on diverse projects providing high quality services to our clients. Join our team where your contribution matters. CEC is an EEO employer - M/F/Veterans/Disabled.
Feb 17, 2020
Full time
Overview As an Air Quality Scientist / Engineer for Civil & Environmental Consultants, Inc. (CEC), you will evaluate and present information regarding atmospheric emissions from proposed processes and equipment in support of state and federal permit applications. Job duties will include performing engineering calculations, compiling permit application documents, meeting and coordinating with clients to obtain and understand project information, communicating with agency personnel, and evaluating control technologies for client facilities. Qualifications BS or MS in Environmental Engineering, Chemical Engineering, Environmental Sciences, Meteorology, or related fields; Experience with atmospheric emission inventory calculations, air permit application preparation, and pollution control technologies; and Excellent written and verbal communication skills; 8+ years consulting, compliance, or industry experience; Knowledge of PA, OH, WV Regulations, and USEPA air quality regulations; Knowledge of New Source Review procedures; Familiarity with air compliance needs of the natural gas, manufacturing, or power industries; and Strong experience with air permitting and compliance for the oil and gas industry. About Us CEC offers big firm opportunities with a small firm culture. We understand the importance of professional growth and offer career advancement and leadership opportunities. You will work on diverse projects providing high quality services to our clients. Join our team where your contribution matters. CEC is an EEO employer - M/F/Veterans/Disabled.
With operations in 35+ nations and ~ 20,000 employees worldwide, CSL is driven to develop and deliver a broad range of lifesaving therapies to treat disorders such as hemophilia and primary immune deficiencies, and vaccines to prevent influenza. Our therapies are also used in cardiac surgery, organ transplantation and burn treatment. CSL is the parent company of CSL Behring and Seqirus. CSL Behring is a global leader in the protein biotherapeutics industry, focused on bringing to market biotherapies used to treat serious and often rare conditions. CSL Behring operates CSL Plasma, one of the world's largest collectors of human plasma, which is used to create CSL's therapies. Seqirus is the second largest influenza vaccine company in the world and is a transcontinental partner in pandemic preparedness and a major contributor to the prevention and control of influenza globally. We invite you to take a look at the many career possibilities available around the globe and consider building your promising future at CSL by becoming a member of our team! Responsibilities The Clinical Pharmacology and Pharmacometrics team of CSL Behring is seeking a Senior Pharmacometrician/AD Pharmacometrics responsible for activities within specific projects at the pre-clinical stage as well as those across all clinical stages at CSL. This role will contribute to the pharmacometric strategy for projects, regulatory submissions, or interactions with authorities, working in parallel to Clinical Pharmacologists, Clinical Program Directors, and other experienced Clinical Development Team (CDT) colleagues, at a project level to align and set pharmacometrics strategy. This role will also assist in interactions with external consultants or with academic institutions. There is a degree of flexibility with regards to level (see qualifications/experience section below)--depending upon experience, this role can be filled at the Pharmacometrician, Senior Pharmacometrician or Associate Director level. At the Associate Director level, the individual assuming this role will have a strong and proven pharmacokinetic/pharmacometrics knowledge, with demonstrable modelling and simulation skills, and will work in close collaboration with various non-clinical, Research, Clinical R&D, & Commercial Development/Medical Affairs functions. The role will work significantly independently, requiring minimal technical management or guidance. A considerable amount of initiative and strategic thinking will also be expected. This role may also be able to supervise more junior-level Pharmacometricians who will be serving at a project and/or a study level and will also assist in interactions with senior-level external consultants or with academic institutions. Qualifications Responsibilities Lead the implementation of model-based drug development strategies for assigned preclinical, clinical, and lifecycle management projects Manage all necessary hardware and software systems, together with relevant quality processes, for the conduct of in-house pharmacometrics activities. Execute relevant pharmacometric analyses for assigned preclinical, clinical, and lifecycle management projects: non-compartmental PK, PK/PD analyses, population PK and PK/PD, clinical trial simulations, meta-analyses, disease and systems biology modelling, and other modeling and simulation activities as appropriate for the project. Apply innovative analytical methods in pharmacometrics/modelling and simulation to integrate knowledge of pharmacokinetics, pharmacodynamics, patient characteristics and disease states in support of optimal study designs Provide pharmacometrics contributions to regulatory documents including Investigator Brochures, Labelling and those required for regulatory meetings and regulatory filings. Provides resolution of pharmacometrics queries from regulatory agencies, taking a lead role in writing and reviewing responses to regulatory queries Write Modeling & Simulation Analysis Plans and Reports. Provides input for, or leads derivation of, standard operation procedures and best practices in pharmacometrics for the Early Development function Provide technical support to Research in the development of preclinical PK/PD model required for early clinical development strategy, as well as utilizing Pharm-Tox data appropriately to make clinical dosing decisions. Analyze and interpret all study PK, PK/PD and pharmacometric outcomes. Ability to create PK/PD files according to standard specifications and to generate tables and listings as required Develop external alliances with consultants, contract organizations and academic institutions to ensure timely conduct of all pharmacometrics deliverables for projects, to continually keep abreast of the science, as well as development of more junior colleagues in the discipline Input to licensing projects as needed Associate Directors will act as a mentor to junior pharmacometricians, providing strategic and technical guidance for their activities. Capabilities Education: Doctoral degree with demonstrated expertise in pharmacometrics and strong quantitative skills (eg proven experience in most of the following areas: population and PK/PD modelling, mechanistic modelling, systems biology, species scaling methodologies and derivation of first-in-human doses, disease modelling and meta-analyses). Experience: Associate Director: A minimum of 5 years of pharmaceutical industry (or relevant) experience,specifically contributing to pharmacometrics aspects of clinical drug development. Senior Pharmacometrician: A minimum of 3 years, specifically contributing to pharmacometrics aspects of clinical drug development. Pharmacometrician: A minimum of 1 year experience of pharmaceutical industry (or relevant) experience, specifically contributing to the pharmacometrics aspects of clinical drug development. For all levels: In-depth knowledge and experience in advanced PK and PK/PD Advanced pharmacometric knowledge in one of the following core sub-speciality: Systems Pharmacology, advanced Exposure-Response Models, Disease Models, Physiological-Based Pharmacokinetic Models Advanced knowledge and experience of software such as NONMEM, SAS, S-Plus, R, WinNonlin, and other server-based data processing and modelling tools Knowledge of the role of pharmacometrics in drug development and FDA/ICH requirements for drug registration Knowledge and application of statistics, random effects modelling, mixed effects modelling, data mining, population PK/PD analyses and modelling (including nonlinear models), Bayesian methods, clinical utility indices, and Monte-Carlo simulation, and clinical trial design and simulation Ability to understand, lead and implement all aspects of pharmacometrics needs across a variety of disease areas Competencies: Excellent skills in the use of NONMEM, PsN, R, and Phoenix. Excellent communication skills with demonstrated ability to effectively present any aspect of this highly technical field, as well as its plans/strategies, accordingly to various audiences in both verbal and written form. Excellent oral presentation skills. Ability to independently lead, conduct, and communicate pharmacometrics plans/strategies and analyses. Ability to create publications according to international scientific standards. Good interpersonal skills, including a positive and constructive attitude and ability to effectively work in a team Matrix environment. Negotiation and influential skills advantageous. Ability to work collaboratively within a matrixed organization. Worker Type: Employee Worker Sub Type: Regular
Feb 17, 2020
Full time
With operations in 35+ nations and ~ 20,000 employees worldwide, CSL is driven to develop and deliver a broad range of lifesaving therapies to treat disorders such as hemophilia and primary immune deficiencies, and vaccines to prevent influenza. Our therapies are also used in cardiac surgery, organ transplantation and burn treatment. CSL is the parent company of CSL Behring and Seqirus. CSL Behring is a global leader in the protein biotherapeutics industry, focused on bringing to market biotherapies used to treat serious and often rare conditions. CSL Behring operates CSL Plasma, one of the world's largest collectors of human plasma, which is used to create CSL's therapies. Seqirus is the second largest influenza vaccine company in the world and is a transcontinental partner in pandemic preparedness and a major contributor to the prevention and control of influenza globally. We invite you to take a look at the many career possibilities available around the globe and consider building your promising future at CSL by becoming a member of our team! Responsibilities The Clinical Pharmacology and Pharmacometrics team of CSL Behring is seeking a Senior Pharmacometrician/AD Pharmacometrics responsible for activities within specific projects at the pre-clinical stage as well as those across all clinical stages at CSL. This role will contribute to the pharmacometric strategy for projects, regulatory submissions, or interactions with authorities, working in parallel to Clinical Pharmacologists, Clinical Program Directors, and other experienced Clinical Development Team (CDT) colleagues, at a project level to align and set pharmacometrics strategy. This role will also assist in interactions with external consultants or with academic institutions. There is a degree of flexibility with regards to level (see qualifications/experience section below)--depending upon experience, this role can be filled at the Pharmacometrician, Senior Pharmacometrician or Associate Director level. At the Associate Director level, the individual assuming this role will have a strong and proven pharmacokinetic/pharmacometrics knowledge, with demonstrable modelling and simulation skills, and will work in close collaboration with various non-clinical, Research, Clinical R&D, & Commercial Development/Medical Affairs functions. The role will work significantly independently, requiring minimal technical management or guidance. A considerable amount of initiative and strategic thinking will also be expected. This role may also be able to supervise more junior-level Pharmacometricians who will be serving at a project and/or a study level and will also assist in interactions with senior-level external consultants or with academic institutions. Qualifications Responsibilities Lead the implementation of model-based drug development strategies for assigned preclinical, clinical, and lifecycle management projects Manage all necessary hardware and software systems, together with relevant quality processes, for the conduct of in-house pharmacometrics activities. Execute relevant pharmacometric analyses for assigned preclinical, clinical, and lifecycle management projects: non-compartmental PK, PK/PD analyses, population PK and PK/PD, clinical trial simulations, meta-analyses, disease and systems biology modelling, and other modeling and simulation activities as appropriate for the project. Apply innovative analytical methods in pharmacometrics/modelling and simulation to integrate knowledge of pharmacokinetics, pharmacodynamics, patient characteristics and disease states in support of optimal study designs Provide pharmacometrics contributions to regulatory documents including Investigator Brochures, Labelling and those required for regulatory meetings and regulatory filings. Provides resolution of pharmacometrics queries from regulatory agencies, taking a lead role in writing and reviewing responses to regulatory queries Write Modeling & Simulation Analysis Plans and Reports. Provides input for, or leads derivation of, standard operation procedures and best practices in pharmacometrics for the Early Development function Provide technical support to Research in the development of preclinical PK/PD model required for early clinical development strategy, as well as utilizing Pharm-Tox data appropriately to make clinical dosing decisions. Analyze and interpret all study PK, PK/PD and pharmacometric outcomes. Ability to create PK/PD files according to standard specifications and to generate tables and listings as required Develop external alliances with consultants, contract organizations and academic institutions to ensure timely conduct of all pharmacometrics deliverables for projects, to continually keep abreast of the science, as well as development of more junior colleagues in the discipline Input to licensing projects as needed Associate Directors will act as a mentor to junior pharmacometricians, providing strategic and technical guidance for their activities. Capabilities Education: Doctoral degree with demonstrated expertise in pharmacometrics and strong quantitative skills (eg proven experience in most of the following areas: population and PK/PD modelling, mechanistic modelling, systems biology, species scaling methodologies and derivation of first-in-human doses, disease modelling and meta-analyses). Experience: Associate Director: A minimum of 5 years of pharmaceutical industry (or relevant) experience,specifically contributing to pharmacometrics aspects of clinical drug development. Senior Pharmacometrician: A minimum of 3 years, specifically contributing to pharmacometrics aspects of clinical drug development. Pharmacometrician: A minimum of 1 year experience of pharmaceutical industry (or relevant) experience, specifically contributing to the pharmacometrics aspects of clinical drug development. For all levels: In-depth knowledge and experience in advanced PK and PK/PD Advanced pharmacometric knowledge in one of the following core sub-speciality: Systems Pharmacology, advanced Exposure-Response Models, Disease Models, Physiological-Based Pharmacokinetic Models Advanced knowledge and experience of software such as NONMEM, SAS, S-Plus, R, WinNonlin, and other server-based data processing and modelling tools Knowledge of the role of pharmacometrics in drug development and FDA/ICH requirements for drug registration Knowledge and application of statistics, random effects modelling, mixed effects modelling, data mining, population PK/PD analyses and modelling (including nonlinear models), Bayesian methods, clinical utility indices, and Monte-Carlo simulation, and clinical trial design and simulation Ability to understand, lead and implement all aspects of pharmacometrics needs across a variety of disease areas Competencies: Excellent skills in the use of NONMEM, PsN, R, and Phoenix. Excellent communication skills with demonstrated ability to effectively present any aspect of this highly technical field, as well as its plans/strategies, accordingly to various audiences in both verbal and written form. Excellent oral presentation skills. Ability to independently lead, conduct, and communicate pharmacometrics plans/strategies and analyses. Ability to create publications according to international scientific standards. Good interpersonal skills, including a positive and constructive attitude and ability to effectively work in a team Matrix environment. Negotiation and influential skills advantageous. Ability to work collaboratively within a matrixed organization. Worker Type: Employee Worker Sub Type: Regular
Teach in England by joining a British government funded and supported teaching program called Quantum Scholars. The program operates throughout England and provides a wonderful and unique opportunity to middle/high school computer science teachers to secure a long term position. We are currently recruiting for positions starting from September 2020. Quantum Scholars works directly with the Department for Education in a highly successful program now entering its third year. The program is very much available to computer science teachers looking to teach in London. We also recruit for math and science teachers. We provide comprehensive support to all certified middle/high school computer science teachers during the relocation phase along with guidance and support during the visa process. A financial rewards benefits package is also on offer to candidates that includes your flight to England being reimbursed up to £700. Not only will you have the opportunity to teach in England with a vast choice of schools, you'll receive outstanding subject-specific Continued Professional Development and ongoing support from a school based mentor. Computer Science teachers also have the opportunity to gain an in-depth knowledge and understanding of current UK pedagogy prior to starting their teaching courtesy of a highly informative induction week. Why teach in England through this program? Teach computer science in a leading school in England at the forefront for education Be carefully matched with a school committed to your development and suited to your character and skills-set Participate in a week-long induction at a top London University to introduce you to current pedagogy before you begin teaching Receive on-going support from a school-based mentor Engage in professional support from a Quantum Scholars mentor Be fully supported with subject specific CPD
Feb 17, 2020
Full time
Teach in England by joining a British government funded and supported teaching program called Quantum Scholars. The program operates throughout England and provides a wonderful and unique opportunity to middle/high school computer science teachers to secure a long term position. We are currently recruiting for positions starting from September 2020. Quantum Scholars works directly with the Department for Education in a highly successful program now entering its third year. The program is very much available to computer science teachers looking to teach in London. We also recruit for math and science teachers. We provide comprehensive support to all certified middle/high school computer science teachers during the relocation phase along with guidance and support during the visa process. A financial rewards benefits package is also on offer to candidates that includes your flight to England being reimbursed up to £700. Not only will you have the opportunity to teach in England with a vast choice of schools, you'll receive outstanding subject-specific Continued Professional Development and ongoing support from a school based mentor. Computer Science teachers also have the opportunity to gain an in-depth knowledge and understanding of current UK pedagogy prior to starting their teaching courtesy of a highly informative induction week. Why teach in England through this program? Teach computer science in a leading school in England at the forefront for education Be carefully matched with a school committed to your development and suited to your character and skills-set Participate in a week-long induction at a top London University to introduce you to current pedagogy before you begin teaching Receive on-going support from a school-based mentor Engage in professional support from a Quantum Scholars mentor Be fully supported with subject specific CPD
Teach in England by joining a British government funded and supported teaching program called Quantum Scholars. The program operates throughout England and provides a wonderful and unique opportunity to middle/high school computer science teachers to secure a long term position. We are currently recruiting for positions starting from September 2020. Quantum Scholars works directly with the Department for Education in a highly successful program now entering its third year. The program is very much available to computer science teachers looking to teach in London. We also recruit for math and science teachers. We provide comprehensive support to all certified middle/high school computer science teachers during the relocation phase along with guidance and support during the visa process. A financial rewards benefits package is also on offer to candidates that includes your flight to England being reimbursed up to £700. Not only will you have the opportunity to teach in England with a vast choice of schools, you'll receive outstanding subject-specific Continued Professional Development and ongoing support from a school based mentor. Computer Science teachers also have the opportunity to gain an in-depth knowledge and understanding of current UK pedagogy prior to starting their teaching courtesy of a highly informative induction week. Why teach in England through this program? Teach computer science in a leading school in England at the forefront for education Be carefully matched with a school committed to your development and suited to your character and skills-set Participate in a week-long induction at a top London University to introduce you to current pedagogy before you begin teaching Receive on-going support from a school-based mentor Engage in professional support from a Quantum Scholars mentor Be fully supported with subject specific CPD
Feb 17, 2020
Full time
Teach in England by joining a British government funded and supported teaching program called Quantum Scholars. The program operates throughout England and provides a wonderful and unique opportunity to middle/high school computer science teachers to secure a long term position. We are currently recruiting for positions starting from September 2020. Quantum Scholars works directly with the Department for Education in a highly successful program now entering its third year. The program is very much available to computer science teachers looking to teach in London. We also recruit for math and science teachers. We provide comprehensive support to all certified middle/high school computer science teachers during the relocation phase along with guidance and support during the visa process. A financial rewards benefits package is also on offer to candidates that includes your flight to England being reimbursed up to £700. Not only will you have the opportunity to teach in England with a vast choice of schools, you'll receive outstanding subject-specific Continued Professional Development and ongoing support from a school based mentor. Computer Science teachers also have the opportunity to gain an in-depth knowledge and understanding of current UK pedagogy prior to starting their teaching courtesy of a highly informative induction week. Why teach in England through this program? Teach computer science in a leading school in England at the forefront for education Be carefully matched with a school committed to your development and suited to your character and skills-set Participate in a week-long induction at a top London University to introduce you to current pedagogy before you begin teaching Receive on-going support from a school-based mentor Engage in professional support from a Quantum Scholars mentor Be fully supported with subject specific CPD
Teach in England by joining a British government funded and supported teaching program called Quantum Scholars. The program operates throughout England and provides a wonderful and unique opportunity to middle/high school computer science teachers to secure a long term position. We are currently recruiting for positions starting from September 2020. Quantum Scholars works directly with the Department for Education in a highly successful program now entering its third year. The program is very much available to computer science teachers looking to teach in London. We also recruit for math and science teachers. We provide comprehensive support to all certified middle/high school computer science teachers during the relocation phase along with guidance and support during the visa process. A financial rewards benefits package is also on offer to candidates that includes your flight to England being reimbursed up to £700. Not only will you have the opportunity to teach in England with a vast choice of schools, you'll receive outstanding subject-specific Continued Professional Development and ongoing support from a school based mentor. Computer Science teachers also have the opportunity to gain an in-depth knowledge and understanding of current UK pedagogy prior to starting their teaching courtesy of a highly informative induction week. Why teach in England through this program? Teach computer science in a leading school in England at the forefront for education Be carefully matched with a school committed to your development and suited to your character and skills-set Participate in a week-long induction at a top London University to introduce you to current pedagogy before you begin teaching Receive on-going support from a school-based mentor Engage in professional support from a Quantum Scholars mentor Be fully supported with subject specific CPD
Feb 17, 2020
Full time
Teach in England by joining a British government funded and supported teaching program called Quantum Scholars. The program operates throughout England and provides a wonderful and unique opportunity to middle/high school computer science teachers to secure a long term position. We are currently recruiting for positions starting from September 2020. Quantum Scholars works directly with the Department for Education in a highly successful program now entering its third year. The program is very much available to computer science teachers looking to teach in London. We also recruit for math and science teachers. We provide comprehensive support to all certified middle/high school computer science teachers during the relocation phase along with guidance and support during the visa process. A financial rewards benefits package is also on offer to candidates that includes your flight to England being reimbursed up to £700. Not only will you have the opportunity to teach in England with a vast choice of schools, you'll receive outstanding subject-specific Continued Professional Development and ongoing support from a school based mentor. Computer Science teachers also have the opportunity to gain an in-depth knowledge and understanding of current UK pedagogy prior to starting their teaching courtesy of a highly informative induction week. Why teach in England through this program? Teach computer science in a leading school in England at the forefront for education Be carefully matched with a school committed to your development and suited to your character and skills-set Participate in a week-long induction at a top London University to introduce you to current pedagogy before you begin teaching Receive on-going support from a school-based mentor Engage in professional support from a Quantum Scholars mentor Be fully supported with subject specific CPD
Teach in England by joining a British government funded and supported teaching program called Quantum Scholars. The program operates throughout England and provides a wonderful and unique opportunity to middle/high school computer science teachers to secure a long term position. We are currently recruiting for positions starting from September 2020. Quantum Scholars works directly with the Department for Education in a highly successful program now entering its third year. The program is very much available to computer science teachers looking to teach in London. We also recruit for math and science teachers. We provide comprehensive support to all certified middle/high school computer science teachers during the relocation phase along with guidance and support during the visa process. A financial rewards benefits package is also on offer to candidates that includes your flight to England being reimbursed up to £700. Not only will you have the opportunity to teach in England with a vast choice of schools, you'll receive outstanding subject-specific Continued Professional Development and ongoing support from a school based mentor. Computer Science teachers also have the opportunity to gain an in-depth knowledge and understanding of current UK pedagogy prior to starting their teaching courtesy of a highly informative induction week. Why teach in England through this program? Teach computer science in a leading school in England at the forefront for education Be carefully matched with a school committed to your development and suited to your character and skills-set Participate in a week-long induction at a top London University to introduce you to current pedagogy before you begin teaching Receive on-going support from a school-based mentor Engage in professional support from a Quantum Scholars mentor Be fully supported with subject specific CPD
Feb 17, 2020
Full time
Teach in England by joining a British government funded and supported teaching program called Quantum Scholars. The program operates throughout England and provides a wonderful and unique opportunity to middle/high school computer science teachers to secure a long term position. We are currently recruiting for positions starting from September 2020. Quantum Scholars works directly with the Department for Education in a highly successful program now entering its third year. The program is very much available to computer science teachers looking to teach in London. We also recruit for math and science teachers. We provide comprehensive support to all certified middle/high school computer science teachers during the relocation phase along with guidance and support during the visa process. A financial rewards benefits package is also on offer to candidates that includes your flight to England being reimbursed up to £700. Not only will you have the opportunity to teach in England with a vast choice of schools, you'll receive outstanding subject-specific Continued Professional Development and ongoing support from a school based mentor. Computer Science teachers also have the opportunity to gain an in-depth knowledge and understanding of current UK pedagogy prior to starting their teaching courtesy of a highly informative induction week. Why teach in England through this program? Teach computer science in a leading school in England at the forefront for education Be carefully matched with a school committed to your development and suited to your character and skills-set Participate in a week-long induction at a top London University to introduce you to current pedagogy before you begin teaching Receive on-going support from a school-based mentor Engage in professional support from a Quantum Scholars mentor Be fully supported with subject specific CPD
Nomad Health, the modern healthcare staffing company, seeks an experienced registered nurse for this rewarding travel assignment opportunity. Join Nomad's growing team of registered nursing professionals. Nomad offers nurses a hassle-free experience, industry-leading pay rates, full benefits, and exceptional service. Earn more. Stress less. Be a Nomad! Start Date: Immediate Start QUALIFICATIONS Active Registered Nurse license in the specified state. RN degree from an accredited registered nurse program. BLS and all relevant specialty/department-specific certifications required. Two years of RN experience and 1 year of recent experience in the specialty. NOMAD BENEFITS Housing: Stipend provided. Best-in-class availability through our housing partner. Travel: Up to $1,000 reimbursement for travel to your assignment. Medical/Dental: Major medical and dental plans available from your first day of work. Payroll: Weekly deposits direct to your bank account. PandoLogic. Category: , Keywords: Certified Registered Nurse (RN) - Midwife
Feb 17, 2020
Full time
Nomad Health, the modern healthcare staffing company, seeks an experienced registered nurse for this rewarding travel assignment opportunity. Join Nomad's growing team of registered nursing professionals. Nomad offers nurses a hassle-free experience, industry-leading pay rates, full benefits, and exceptional service. Earn more. Stress less. Be a Nomad! Start Date: Immediate Start QUALIFICATIONS Active Registered Nurse license in the specified state. RN degree from an accredited registered nurse program. BLS and all relevant specialty/department-specific certifications required. Two years of RN experience and 1 year of recent experience in the specialty. NOMAD BENEFITS Housing: Stipend provided. Best-in-class availability through our housing partner. Travel: Up to $1,000 reimbursement for travel to your assignment. Medical/Dental: Major medical and dental plans available from your first day of work. Payroll: Weekly deposits direct to your bank account. PandoLogic. Category: , Keywords: Certified Registered Nurse (RN) - Midwife
Overview About the Organization Tower Health is a strong, regional, integrated healthcare provider/payer system that offers leading-edge, compassionate healthcare and wellness services to a population of 2.5 million people. Together, our seven hospitals and other entities provide a full range of medical care from prevention, screenings & education; to the latest clinical services and surgeries available; to rehabilitation. We also offer wellness programs & public health services that ensure our communities are the healthiest they can be. Our caring, highly trained physicians and staff are committed to patient safety and patient satisfaction. With more than 11,000 team members, Tower Health includes Reading Hospital, a teaching hospital based in West Reading; Brandywine Hospital in Coatesville; Chestnut Hill Hospital, a teaching hospital in Philadelphia; Jennersville Hospital in West Grove; Phoenixville Hospital in Phoenixville; Pottstown Hospital in Pottstown; and St. Christopher's Hospital for Children. We also operate Reading Hospital Rehabilitation at Wyomissing & Reading Hospital School of Health Sciences, & we have a comprehensive physician network. Collaboration across Tower Health enables our hospitals, providers, leadership & staff to leverage best practices across the health system. Our hospitals have received national recognition for advanced care in areas such as neurosurgery and stroke, cardiac & vascular surgery, trauma, hematology & oncology. Reading HealthPlex, which opened at Reading Hospital in October 2016, combines state-of-the-art technology and world-class design to make the HealthPlex one of the most sophisticated surgical centers & inpatient facilities in the region. At Tower Health, we have a rich history of providing high-quality, cost-effective care in the communities we serve. As the healthcare industry continues to change, one thing remains steadfast: Tower Health's commitment to Advancing Health, Transforming Lives. Responsibilities The Pharmacist is responsible for assisting in the planning, organization and direction of clinical pharamceutical services to achieve high- quality standard-of-care in pharmacy services to the critical care areas. Provides specialized pharmaceutical services to imporve drug usage and therapeutic outcomes for critical care patients. Directly covert from IV to oral therapy per hospital protocol. Develop formulary assessment material and play a key role in evaluation critical care related formulary items. Continually improves the delivery of pharamceutical care to patients in the critical care areas and serves as a resource for other Pharamcists in the department who service the critical care areas. Participates on multidisciplinary teams related to critical care. Participates in the development and delivery of critical care related continuing education programs for the Pharmacy department. Participates in the preception and education of pharmacy students. Achieves and maintains satisfactory working relationships with physicians, nurses, dieticians, respiratory therapists, pharmacy staff, other clinicians and hospital staff. Qualifications Must have a Pharmacy degree (Bachelor of Sciense or Pharm.D.) Successful completion of a post-graduate residency or equivalent experience in critical care is required. Possess a valid Pennsylvania State License from the Pennsylvania Board of Pharmacy or be board eligible for Pharmacy Licensure.
Feb 17, 2020
Full time
Overview About the Organization Tower Health is a strong, regional, integrated healthcare provider/payer system that offers leading-edge, compassionate healthcare and wellness services to a population of 2.5 million people. Together, our seven hospitals and other entities provide a full range of medical care from prevention, screenings & education; to the latest clinical services and surgeries available; to rehabilitation. We also offer wellness programs & public health services that ensure our communities are the healthiest they can be. Our caring, highly trained physicians and staff are committed to patient safety and patient satisfaction. With more than 11,000 team members, Tower Health includes Reading Hospital, a teaching hospital based in West Reading; Brandywine Hospital in Coatesville; Chestnut Hill Hospital, a teaching hospital in Philadelphia; Jennersville Hospital in West Grove; Phoenixville Hospital in Phoenixville; Pottstown Hospital in Pottstown; and St. Christopher's Hospital for Children. We also operate Reading Hospital Rehabilitation at Wyomissing & Reading Hospital School of Health Sciences, & we have a comprehensive physician network. Collaboration across Tower Health enables our hospitals, providers, leadership & staff to leverage best practices across the health system. Our hospitals have received national recognition for advanced care in areas such as neurosurgery and stroke, cardiac & vascular surgery, trauma, hematology & oncology. Reading HealthPlex, which opened at Reading Hospital in October 2016, combines state-of-the-art technology and world-class design to make the HealthPlex one of the most sophisticated surgical centers & inpatient facilities in the region. At Tower Health, we have a rich history of providing high-quality, cost-effective care in the communities we serve. As the healthcare industry continues to change, one thing remains steadfast: Tower Health's commitment to Advancing Health, Transforming Lives. Responsibilities The Pharmacist is responsible for assisting in the planning, organization and direction of clinical pharamceutical services to achieve high- quality standard-of-care in pharmacy services to the critical care areas. Provides specialized pharmaceutical services to imporve drug usage and therapeutic outcomes for critical care patients. Directly covert from IV to oral therapy per hospital protocol. Develop formulary assessment material and play a key role in evaluation critical care related formulary items. Continually improves the delivery of pharamceutical care to patients in the critical care areas and serves as a resource for other Pharamcists in the department who service the critical care areas. Participates on multidisciplinary teams related to critical care. Participates in the development and delivery of critical care related continuing education programs for the Pharmacy department. Participates in the preception and education of pharmacy students. Achieves and maintains satisfactory working relationships with physicians, nurses, dieticians, respiratory therapists, pharmacy staff, other clinicians and hospital staff. Qualifications Must have a Pharmacy degree (Bachelor of Sciense or Pharm.D.) Successful completion of a post-graduate residency or equivalent experience in critical care is required. Possess a valid Pennsylvania State License from the Pennsylvania Board of Pharmacy or be board eligible for Pharmacy Licensure.
Responsibilities The Pharmacy Intern is a student enrolled in an accredited school of pharmacy completing hour requirements necessary for the PharmD degree. The pharmacy intern will participate in advanced technician training and student clinical training provided by the Reading Hospital Department of Pharmacy. The pharmacy intern will provide collaborative pharmaceutical care through integrated drug distribution, consistent service, and interactions with interdisciplinary and multidisciplinary teams within the health system. During the summer, the intern will work full time evening hours rotating weekend, holidays. During the rest of the school year the intern will work part time hours. Qualifications Must have High School Diploma or GED Must be enrolled in an accredited school of pharmacy completing hour requirements necessary for the PharmD degree. Must have completed at least 1 Professional Year.
Feb 17, 2020
Full time
Responsibilities The Pharmacy Intern is a student enrolled in an accredited school of pharmacy completing hour requirements necessary for the PharmD degree. The pharmacy intern will participate in advanced technician training and student clinical training provided by the Reading Hospital Department of Pharmacy. The pharmacy intern will provide collaborative pharmaceutical care through integrated drug distribution, consistent service, and interactions with interdisciplinary and multidisciplinary teams within the health system. During the summer, the intern will work full time evening hours rotating weekend, holidays. During the rest of the school year the intern will work part time hours. Qualifications Must have High School Diploma or GED Must be enrolled in an accredited school of pharmacy completing hour requirements necessary for the PharmD degree. Must have completed at least 1 Professional Year.
Responsibilities A Pharmacy Technician assists the pharmacist in his/her professional responsibilities in providing pharmacy services. Working under the direction of a licensed pharmacist, participates in the preparation, dispensing, distribution and return of patient specific medications including intravenous admixtures, supplies and maintains automated technology equipment, packages unit of use dosages, maintains and transports pharmaceuticals, and performs tasks associated with regulatory compliance. Documents activities as indicated and performs other duties as required. #LI Qualifications EDUCATION REQUIREMENTS High School Diploma or GED EXPERIENCE Previous experience preferred. CERTIFICATION AND LICENSURE REQUIREMENTS National Pharmacy Technician Certification (CPhT) through the Pharmacy Technician Certification Board (PTCB) Required upon hire or within the first 6 months of employment REQUIRED SKILLS Excellent Communications Skills, Interpersonal Skills, Multi Line Telephone Operational Skills, Computer Skills to include use and navigation, and Good Reasoning Skills
Feb 17, 2020
Full time
Responsibilities A Pharmacy Technician assists the pharmacist in his/her professional responsibilities in providing pharmacy services. Working under the direction of a licensed pharmacist, participates in the preparation, dispensing, distribution and return of patient specific medications including intravenous admixtures, supplies and maintains automated technology equipment, packages unit of use dosages, maintains and transports pharmaceuticals, and performs tasks associated with regulatory compliance. Documents activities as indicated and performs other duties as required. #LI Qualifications EDUCATION REQUIREMENTS High School Diploma or GED EXPERIENCE Previous experience preferred. CERTIFICATION AND LICENSURE REQUIREMENTS National Pharmacy Technician Certification (CPhT) through the Pharmacy Technician Certification Board (PTCB) Required upon hire or within the first 6 months of employment REQUIRED SKILLS Excellent Communications Skills, Interpersonal Skills, Multi Line Telephone Operational Skills, Computer Skills to include use and navigation, and Good Reasoning Skills
Overview About the Organization Tower Health is a strong, regional, integrated healthcare provider/payer system that offers leading-edge, compassionate healthcare and wellness services to a population of 2.5 million people. Together, our seven hospitals and other entities provide a full range of medical care from prevention, screenings & education; to the latest clinical services and surgeries available; to rehabilitation. We also offer wellness programs & public health services that ensure our communities are the healthiest they can be. Our caring, highly trained physicians and staff are committed to patient safety and patient satisfaction. With more than 11,000 team members, Tower Health includes Reading Hospital, a teaching hospital based in West Reading; Brandywine Hospital in Coatesville; Chestnut Hill Hospital, a teaching hospital in Philadelphia; Jennersville Hospital in West Grove; Phoenixville Hospital in Phoenixville; Pottstown Hospital in Pottstown; and St. Christopher's Hospital for Children. We also operate Reading Hospital Rehabilitation at Wyomissing & Reading Hospital School of Health Sciences, & we have a comprehensive physician network. Collaboration across Tower Health enables our hospitals, providers, leadership & staff to leverage best practices across the health system. Our hospitals have received national recognition for advanced care in areas such as neurosurgery and stroke, cardiac & vascular surgery, trauma, hematology & oncology. Reading HealthPlex, which opened at Reading Hospital in October 2016, combines state-of-the-art technology and world-class design to make the HealthPlex one of the most sophisticated surgical centers & inpatient facilities in the region. At Tower Health, we have a rich history of providing high-quality, cost-effective care in the communities we serve. As the healthcare industry continues to change, one thing remains steadfast: Tower Health's commitment to Advancing Health, Transforming Lives. Responsibilities The Pharmacist is responsible for assisting in the planning, organization and direction of clinical pharamceutical services to achieve high- quality standard-of-care in pharmacy services to the critical care areas. Provides specialized pharmaceutical services to imporve drug usage and therapeutic outcomes for critical care patients. Directly covert from IV to oral therapy per hospital protocol. Develop formulary assessment material and play a key role in evaluation critical care related formulary items. Continually improves the delivery of pharamceutical care to patients in the critical care areas and serves as a resource for other Pharamcists in the department who service the critical care areas. Participates on multidisciplinary teams related to critical care. Participates in the development and delivery of critical care related continuing education programs for the Pharmacy department. Participates in the preception and education of pharmacy students. Achieves and maintains satisfactory working relationships with physicians, nurses, dieticians, respiratory therapists, pharmacy staff, other clinicians and hospital staff. Qualifications Must have a Pharmacy degree (Bachelor of Sciense or Pharm.D.) Successful completion of a post-graduate residency or equivalent experience in critical care is required. Possess a valid Pennsylvania State License from the Pennsylvania Board of Pharmacy or be board eligible for Pharmacy Licensure.
Feb 17, 2020
Full time
Overview About the Organization Tower Health is a strong, regional, integrated healthcare provider/payer system that offers leading-edge, compassionate healthcare and wellness services to a population of 2.5 million people. Together, our seven hospitals and other entities provide a full range of medical care from prevention, screenings & education; to the latest clinical services and surgeries available; to rehabilitation. We also offer wellness programs & public health services that ensure our communities are the healthiest they can be. Our caring, highly trained physicians and staff are committed to patient safety and patient satisfaction. With more than 11,000 team members, Tower Health includes Reading Hospital, a teaching hospital based in West Reading; Brandywine Hospital in Coatesville; Chestnut Hill Hospital, a teaching hospital in Philadelphia; Jennersville Hospital in West Grove; Phoenixville Hospital in Phoenixville; Pottstown Hospital in Pottstown; and St. Christopher's Hospital for Children. We also operate Reading Hospital Rehabilitation at Wyomissing & Reading Hospital School of Health Sciences, & we have a comprehensive physician network. Collaboration across Tower Health enables our hospitals, providers, leadership & staff to leverage best practices across the health system. Our hospitals have received national recognition for advanced care in areas such as neurosurgery and stroke, cardiac & vascular surgery, trauma, hematology & oncology. Reading HealthPlex, which opened at Reading Hospital in October 2016, combines state-of-the-art technology and world-class design to make the HealthPlex one of the most sophisticated surgical centers & inpatient facilities in the region. At Tower Health, we have a rich history of providing high-quality, cost-effective care in the communities we serve. As the healthcare industry continues to change, one thing remains steadfast: Tower Health's commitment to Advancing Health, Transforming Lives. Responsibilities The Pharmacist is responsible for assisting in the planning, organization and direction of clinical pharamceutical services to achieve high- quality standard-of-care in pharmacy services to the critical care areas. Provides specialized pharmaceutical services to imporve drug usage and therapeutic outcomes for critical care patients. Directly covert from IV to oral therapy per hospital protocol. Develop formulary assessment material and play a key role in evaluation critical care related formulary items. Continually improves the delivery of pharamceutical care to patients in the critical care areas and serves as a resource for other Pharamcists in the department who service the critical care areas. Participates on multidisciplinary teams related to critical care. Participates in the development and delivery of critical care related continuing education programs for the Pharmacy department. Participates in the preception and education of pharmacy students. Achieves and maintains satisfactory working relationships with physicians, nurses, dieticians, respiratory therapists, pharmacy staff, other clinicians and hospital staff. Qualifications Must have a Pharmacy degree (Bachelor of Sciense or Pharm.D.) Successful completion of a post-graduate residency or equivalent experience in critical care is required. Possess a valid Pennsylvania State License from the Pennsylvania Board of Pharmacy or be board eligible for Pharmacy Licensure.
Responsibilities The Pharmacy Intern is a student enrolled in an accredited school of pharmacy completing hour requirements necessary for the PharmD degree. The pharmacy intern will participate in advanced technician training and student clinical training provided by the Reading Hospital Department of Pharmacy. The pharmacy intern will provide collaborative pharmaceutical care through integrated drug distribution, consistent service, and interactions with interdisciplinary and multidisciplinary teams within the health system. During the summer, the intern will work full time evening hours rotating weekend, holidays. During the rest of the school year the intern will work part time hours. Qualifications Must have High School Diploma or GED Must be enrolled in an accredited school of pharmacy completing hour requirements necessary for the PharmD degree. Must have completed at least 1 Professional Year.
Feb 17, 2020
Full time
Responsibilities The Pharmacy Intern is a student enrolled in an accredited school of pharmacy completing hour requirements necessary for the PharmD degree. The pharmacy intern will participate in advanced technician training and student clinical training provided by the Reading Hospital Department of Pharmacy. The pharmacy intern will provide collaborative pharmaceutical care through integrated drug distribution, consistent service, and interactions with interdisciplinary and multidisciplinary teams within the health system. During the summer, the intern will work full time evening hours rotating weekend, holidays. During the rest of the school year the intern will work part time hours. Qualifications Must have High School Diploma or GED Must be enrolled in an accredited school of pharmacy completing hour requirements necessary for the PharmD degree. Must have completed at least 1 Professional Year.
Responsibilities A Pharmacy Technician assists the pharmacist in his/her professional responsibilities in providing pharmacy services. Working under the direction of a licensed pharmacist, participates in the preparation, dispensing, distribution and return of patient specific medications including intravenous admixtures, supplies and maintains automated technology equipment, packages unit of use dosages, maintains and transports pharmaceuticals, and performs tasks associated with regulatory compliance. Documents activities as indicated and performs other duties as required. #LI Qualifications EDUCATION REQUIREMENTS High School Diploma or GED EXPERIENCE Previous experience preferred. CERTIFICATION AND LICENSURE REQUIREMENTS National Pharmacy Technician Certification (CPhT) through the Pharmacy Technician Certification Board (PTCB) Required upon hire or within the first 6 months of employment REQUIRED SKILLS Excellent Communications Skills, Interpersonal Skills, Multi Line Telephone Operational Skills, Computer Skills to include use and navigation, and Good Reasoning Skills
Feb 17, 2020
Full time
Responsibilities A Pharmacy Technician assists the pharmacist in his/her professional responsibilities in providing pharmacy services. Working under the direction of a licensed pharmacist, participates in the preparation, dispensing, distribution and return of patient specific medications including intravenous admixtures, supplies and maintains automated technology equipment, packages unit of use dosages, maintains and transports pharmaceuticals, and performs tasks associated with regulatory compliance. Documents activities as indicated and performs other duties as required. #LI Qualifications EDUCATION REQUIREMENTS High School Diploma or GED EXPERIENCE Previous experience preferred. CERTIFICATION AND LICENSURE REQUIREMENTS National Pharmacy Technician Certification (CPhT) through the Pharmacy Technician Certification Board (PTCB) Required upon hire or within the first 6 months of employment REQUIRED SKILLS Excellent Communications Skills, Interpersonal Skills, Multi Line Telephone Operational Skills, Computer Skills to include use and navigation, and Good Reasoning Skills
As a Lab Technician in an Aspen Dental-branded practice you're not only making a statement that you're committed to providing quality dental care but you're also becoming a part of a collaborative community of dental professionals. For an estimated 47 million Americans, lack of access to affordable dental care is a serious problem and Aspen Dental is transforming healthcare by breaking down the barriers to better care, better smiles and better lives. Lab technicians with Aspen Dental work for Aspen Dental Management, Inc. (ADMI), a dental support organization that provides all non-clinical support services to Aspen Dental-branded practices. As a lab technician with ADMI, you'll work on-site in a modern Aspen Dental practice handcrafting high-quality full and partial dentures. With state-of-the-art equipment and instruments on site, you'll have the best tools at your disposal. You'll also enjoy regular hours, technical training, a competitive salary and benefit package as well as the opportunity to advance into a managerial role. With an average of six new patients per day, you'll be a part of the patient experience from impression to insert. You'll work alongside the dentist in the office, offering your expertise to ensure patients receive quality and timely service. About Aspen Dental Management, Inc. Aspen Dental-branded practices are supported by ADMI, a dental support organization that provides non-clinical business support to licensed, independent dentists. Fabricate high quality denture prosthetics. Complete prosthetic repairs, relines and re-bases. Operate within all company-established protocols Preparation of laboratory supply orders while staying within determined budgetary guidelines. Collaborate with dentists to ensure optimum patient satisfaction. Advanced training in dental lab technology preferred. Minimum 2 years proven experience with the complete fabrication of quality prosthetic denture products from start to finish.
Feb 17, 2020
Full time
As a Lab Technician in an Aspen Dental-branded practice you're not only making a statement that you're committed to providing quality dental care but you're also becoming a part of a collaborative community of dental professionals. For an estimated 47 million Americans, lack of access to affordable dental care is a serious problem and Aspen Dental is transforming healthcare by breaking down the barriers to better care, better smiles and better lives. Lab technicians with Aspen Dental work for Aspen Dental Management, Inc. (ADMI), a dental support organization that provides all non-clinical support services to Aspen Dental-branded practices. As a lab technician with ADMI, you'll work on-site in a modern Aspen Dental practice handcrafting high-quality full and partial dentures. With state-of-the-art equipment and instruments on site, you'll have the best tools at your disposal. You'll also enjoy regular hours, technical training, a competitive salary and benefit package as well as the opportunity to advance into a managerial role. With an average of six new patients per day, you'll be a part of the patient experience from impression to insert. You'll work alongside the dentist in the office, offering your expertise to ensure patients receive quality and timely service. About Aspen Dental Management, Inc. Aspen Dental-branded practices are supported by ADMI, a dental support organization that provides non-clinical business support to licensed, independent dentists. Fabricate high quality denture prosthetics. Complete prosthetic repairs, relines and re-bases. Operate within all company-established protocols Preparation of laboratory supply orders while staying within determined budgetary guidelines. Collaborate with dentists to ensure optimum patient satisfaction. Advanced training in dental lab technology preferred. Minimum 2 years proven experience with the complete fabrication of quality prosthetic denture products from start to finish.
Experience Required: 1 to 3 years Experience Desired: Experience in drug handling protocols and best practices in a time-bound fulfillment order process Education Required: High school diploma or equivalent Lifting Requirement: Up to 10 pounds Age Requirement: At least 18 years of age Job Responsibilities Remove out of date and expired medications using proper company procedures. Train and mentor new department Team members. Report errors, omissions and incidents to Pharmacist on duty. Perform, under the direct supervision of a Pharmacist, the direct preparation and filling of a prescription. Prepare and fill non-auto counted drugs. Label bottles and prepackaged items accurately. Replenish canisters with consumables needed for prescription fulfillment. Maintain a neat and clean work environment in order to ensure that company and government requirements are met. Recognize, address and escalate system issues. Adhere to all company, state and federal policies, laws and regulations, including HIPAA. Operate semi-automatic cabinet in order to fill customer orders. Maintain production rates and meet quality expectations as determined by leadership. Perform other duties as assigned.
Feb 17, 2020
Full time
Experience Required: 1 to 3 years Experience Desired: Experience in drug handling protocols and best practices in a time-bound fulfillment order process Education Required: High school diploma or equivalent Lifting Requirement: Up to 10 pounds Age Requirement: At least 18 years of age Job Responsibilities Remove out of date and expired medications using proper company procedures. Train and mentor new department Team members. Report errors, omissions and incidents to Pharmacist on duty. Perform, under the direct supervision of a Pharmacist, the direct preparation and filling of a prescription. Prepare and fill non-auto counted drugs. Label bottles and prepackaged items accurately. Replenish canisters with consumables needed for prescription fulfillment. Maintain a neat and clean work environment in order to ensure that company and government requirements are met. Recognize, address and escalate system issues. Adhere to all company, state and federal policies, laws and regulations, including HIPAA. Operate semi-automatic cabinet in order to fill customer orders. Maintain production rates and meet quality expectations as determined by leadership. Perform other duties as assigned.
Experience Required: 1 to 3 years Experience Desired: Experience in drug handling protocols and best practices in a time-bound fulfillment order process Education Required: High school diploma or equivalent Lifting Requirement: Up to 10 pounds Age Requirement: At least 18 years of age Job Responsibilities Remove out of date and expired medications using proper company procedures. Train and mentor new department Team members. Report errors, omissions and incidents to Pharmacist on duty. Perform, under the direct supervision of a Pharmacist, the direct preparation and filling of a prescription. Prepare and fill non-auto counted drugs. Label bottles and prepackaged items accurately. Replenish canisters with consumables needed for prescription fulfillment. Maintain a neat and clean work environment in order to ensure that company and government requirements are met. Recognize, address and escalate system issues. Adhere to all company, state and federal policies, laws and regulations, including HIPAA. Operate semi-automatic cabinet in order to fill customer orders. Maintain production rates and meet quality expectations as determined by leadership. Perform other duties as assigned.
Feb 17, 2020
Full time
Experience Required: 1 to 3 years Experience Desired: Experience in drug handling protocols and best practices in a time-bound fulfillment order process Education Required: High school diploma or equivalent Lifting Requirement: Up to 10 pounds Age Requirement: At least 18 years of age Job Responsibilities Remove out of date and expired medications using proper company procedures. Train and mentor new department Team members. Report errors, omissions and incidents to Pharmacist on duty. Perform, under the direct supervision of a Pharmacist, the direct preparation and filling of a prescription. Prepare and fill non-auto counted drugs. Label bottles and prepackaged items accurately. Replenish canisters with consumables needed for prescription fulfillment. Maintain a neat and clean work environment in order to ensure that company and government requirements are met. Recognize, address and escalate system issues. Adhere to all company, state and federal policies, laws and regulations, including HIPAA. Operate semi-automatic cabinet in order to fill customer orders. Maintain production rates and meet quality expectations as determined by leadership. Perform other duties as assigned.
