242 jobs found in Tarrytown

Known for its scientific and operational excellence, Regeneron is a leading science-based biopharmaceutical company that discovers, invents, develops, manufactures, and commercializes medicines for the treatment of serious medical conditions. Regeneron commercializes medicines for eye diseases, high LDL-cholesterol, atopic dermatitis and a rare inflammatory condition and has product candidates in development in other areas of high unmet medical need, including rheumatoid arthritis, asthma, pain, cancer and infectious diseases. Summary: The Senior Sourcing Manager will be responsible to support and assist in the development of the Category Management strategy by gathering and anticipating business unit supply needs and specifications for the Commercial organization. She/he works collaboratively with the Category Manager and business unit stakeholders to commercially & competitively assess the local supply base's capabilities and qualifications for Regeneron's interests. The Senior Sourcing Manager owns the local supplier relationship and manages ongoing performance and service delivery. She/he must have demonstrated capability to proactively manage a supply base and maximize value, minimize risk, and ensure quality & cost effectiveness. SCOPE: Local supply markets Responsibilities: • Leads and/or works with others to solve issues of diverse scope where analysis requires an understanding of current business trends • Uses sophisticated analytical thought to exercise judgement and identify innovative solutions • Requires broad understanding of the processes, procedures and systems and is able to use that knowledge to improve efficiency and produce high quality work on problems with cross functional impact • Responsible for specific local contractual agreements, works with internal legal department, and drives any changes that are critical to Regeneron's interest • Develops and executes sourcing strategies for respective area of spend responsibility to optimize value • Solicits and analyzes requests for proposals, negotiates contracts, and ensure contract objectives are delivered (savings, SLAs, etc.); ensures compliance with local pricing agreements and internal policies/procedures • Manages local vendor/supplier relationships and ensures performance and accountability are tracked/improved • Develops and manages program policies and procedures ensuring compliance with Company guidelines, related laws and governmental guidelines • Develops and executes local market procurement related programs to optimize value • Informs and influences decision making at the management level • Manages local supplier integration plans with internal clients for all goods and services for consumption by internal stakeholders, business unit or function • Identifies local supply market projects to apply sourcing and procurement methodologies • Conducts local supplier relationship management activities as guided by the Supplier Management Program to achieve continuous improvement goals • Coaches and develops proficiency in procurement technical skills among direct reports (if applicable), peers, and junior team members Requirements: Education • Bachelor's plus 10 years of relevant, progressive experience within procurement, to preferrably include 7 years directly in sourcing Pharma/Biotech. Or • Master's plus 7 years of relevant, progressive experience within procurement, to preferrably include 7 years directly in sourcing within Pharma/Biotech. • CPSM/CPM preferred Experience • Working knowledge with Sourcing Contracting, ERP, eRFX systems preferred. (Oracle, Zycus, GEP, Ariba, Other) • Ability to leverage standard business applications for communicating, presenting and analyzing (Word, Excel, Powerpoint) • Previous leadership experience preferred. • Advanced level proficiency using negotiations skills • Cost modeling knowledge • Excellent verbal and written skills • Ability to formulate high level presentations and business cases • Ability to build consensus, teamwork, and creativity within a collaborative team with limited supervision • Program management experience and project management experience required This is an opportunity to join our select team that is already leading the way in the Pharmaceutical/Biotech industry. Apply today and learn more about Regeneron's unwavering commitment to combining good science & good business. To all agencies: Please, no phone calls or emails to any employee of Regeneron about this opening. All resumes submitted by search firms/employment agencies to any employee at Regeneron via-email, the internet or in any form and/or method will be deemed the sole property of Regeneron, unless such search firms/employment agencies were engaged by Regeneron for this position and a valid agreement with Regeneron is in place. In the event a candidate who was submitted outside of the Regeneron agency engagement process is hired, no fee or payment of any kind will be paid. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, sexual orientation, gender identity, disability status, protected veteran status, or any other characteristic protected by law.

Known for its scientific and operational excellence, Regeneron is a leading science-based biopharmaceutical company that discovers, invents, develops, manufactures, and commercializes medicines for the treatment of serious medical conditions. Regeneron commercializes medicines for eye diseases, high LDL-cholesterol, atopic dermatitis and a rare inflammatory condition and has product candidates in development in other areas of high unmet medical need, including rheumatoid arthritis, asthma, pain, cancer and infectious diseases. Summary: A senior statistical programmer provides timely support to the study team on all programming matters according to the project strategies in Pharmacometrics Department in DSP. As an integral part of a study, the incumbent provides project leadership and programming support for processing data from clinical studies. Requirements will be identified according to a Statistical Analysis Plan, clinical pharmacolgy reports requirement and programming specifications using internal standards and guidelines. The incumbent assists in providing guidance in implementing and executing the programming and project standards. Supporting the evaluation and development of study requirements and validation plan are also in the scope of this position. Works independently to design and test program logic, coding programs, program documentation and preparation of programs. Meets statistical adhoc requests of senior management. Provides documentation and consistent maintenance of code, logs, and output in a regulated environment. Responsible for transfer data from the LIMS (BA) and clinical data, prepare merged data sets for pharmacokinetic analysis. Create CDISC compliance analysis datasets (SDTM, ADaM) according to the SAP and programming specification Generate tables/figures to include but not limited to: accounting for the disposition of patients and samples, descriptive statistics of pharmacokinetic variables, and results, concentration over time, pharmacokinetic parameters over dose, concentration effect relationship, and PK/PD analyses. Support the electronic data submission for BLA Growth opportunity for this individual is in the area of Pharmacokinetics; both non-compartmental and compartmental, as in the use of NONMEM, pharmacokinetic simulation and population pharmacokinetics. Basic understanding of biostatistics, experienced in data handling, process and analysis Able to take directives and work independently Excellent interpersonal skills Manage and prioritize multiple programs with competing and aggressive time lines with supervision. Support the Preclinical Pharmacokinetics department as needed. Job Duties: Programming and QC of analysis datasets, TFL's or standard tools following Regeneron standard data models or user requirements. Representation of PM programming functions and coordination of activities with cross line functions and communicate shifting timelines and milestones. Integration of data across studies in support of CSS/CSE/CSP. Create, manage and maintain the programming specifications for the analysis datasets utilizing Regeneron tools and methodologies. Support creation and validation of esubmission requirements (i.e. annotated CRF, data export files, define documents). Work in a multidisciplinary study team to provide timely and quality support for analysis and reporting of clinical trials up to regulatory approval, product launch and annual reports. If applicable, develop and provide department training for applications and standard tools developed by the department functions group. Provide programming support for simple presentations and basic statistical ad-hoc requests. Assist in the more complex data presentations. Participate in department working groups; provide input in development of tools and improvement of processes. Requirements: MS. in Statistics, Computer Science, Mathematics, Engineering, Life Science or related discipline with 3+ years of programming experience preferably in processing clinical trial data in the biotechnology, pharmaceutical or health related industry. SAS Certification desirable. Works independently, exercises judgment in interpreting, modifying, and adapting procedures, practices, methods, etc. in accordance with existing policies and standards for application to specific problems or tasks. Strong SAS programming skills in a clinical data environment. Strong understanding of relational database structure. Understanding of reporting systems utilizing multiple data delivery applications. Strong Experience/knowledge with implementing standardization methodology, creation of current CDISC data standards. Demonstrated teamwork and interpersonal skills. Ability to problem solve. Strong verbal and written communication skills in a global environment. Knowledge of pharmaceutical clinical development (i.e. understanding safety deliverables, efficacy analysis, in addition pharmacokinetic/pharmacodynamic and exposure-response is desired) and ability to provide programming support needs for BLA and other regulatory submissions. Ability to organize and manage multiple assignments with challenging timelines for a limited number of personnel. Problem solving and innovative skills that demonstrate initiative and motivation. Familiarity with the development and execution of user requirements, validation plans, operational and performance protocols. SAS (Base, Stat, Macro, graph), basic R knowledge is plus. May report to a Manager or above This is an opportunity to join our select team that is already leading the way in the Pharmaceutical/Biotech industry. Apply today and learn more about Regeneron's unwavering commitment to combining good science & good business. To all agencies: Please, no phone calls or emails to any employee of Regeneron about this opening. All resumes submitted by search firms/employment agencies to any employee at Regeneron via-email, the internet or in any form and/or method will be deemed the sole property of Regeneron, unless such search firms/employment agencies were engaged by Regeneron for this position and a valid agreement with Regeneron is in place. In the event a candidate who was submitted outside of the Regeneron agency engagement process is hired, no fee or payment of any kind will be paid. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, sexual orientation, gender identity, disability status, protected veteran status, or any other characteristic protected by law.

Known for its scientific and operational excellence, Regeneron is a leading science-based biopharmaceutical company that discovers, invents, develops, manufactures, and commercializes medicines for the treatment of serious medical conditions. Regeneron commercializes medicines for eye diseases, high LDL-cholesterol, atopic dermatitis and a rare inflammatory condition and has product candidates in development in other areas of high unmet medical need, including rheumatoid arthritis, asthma, pain, cancer and infectious diseases. Summary: Provide support on all areas of compensation in regards to Regeneron's base, bonus, long-term incentive programs. Primary focus of this role will be to support the compensation team on Workday implementation, and in specific the Global Job Architecture framework and Job Catalog project. Responsibilities: • Contribute to the documentation of process design and support the implementation of compensation program elements in Workday. • Work with the compensation team on the development of job functions and families. Work with project team to review and refine current job level framework, job title nomenclature and rationalization, employee mapping, pay structure review and job documentation. • Drafts sample job descriptions and assists managers and staff members in job description preparation. • Work with the compensation team on any other related project including compensation program analysis, budgeting, and implementation process. • Provide ad-hoc metric analytics as requested. Requirements: • Knowledge of government regulations as they apply to compensation programs. • Knowledge of job architecture framework and job evaluation • Experience in market pay analysis • Strong analytical, computer and communication skills. • Strong understanding of Microsoft Excel application. • Experience with an HRM, such as Workday, preferred Minimum Years of Experience: • Bachelor's degree with 3-4 years compensation experience preferably in the Pharmaceutical or Biotech industry. CCP certification a plus. Experience with an HRM, such as Workday, preferred This is an opportunity to join our select team that is already leading the way in the Pharmaceutical/Biotech industry. Apply today and learn more about Regeneron's unwavering commitment to combining good science & good business. To all agencies: Please, no phone calls or emails to any employee of Regeneron about this opening. All resumes submitted by search firms/employment agencies to any employee at Regeneron via-email, the internet or in any form and/or method will be deemed the sole property of Regeneron, unless such search firms/employment agencies were engaged by Regeneron for this position and a valid agreement with Regeneron is in place. In the event a candidate who was submitted outside of the Regeneron agency engagement process is hired, no fee or payment of any kind will be paid. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, sexual orientation, gender identity, disability status, protected veteran status, or any other characteristic protected by law.

Known for its scientific and operational excellence, Regeneron is a leading science-based biopharmaceutical company that discovers, invents, develops, manufactures, and commercializes medicines for the treatment of serious medical conditions. Regeneron commercializes medicines for eye diseases, high LDL-cholesterol, atopic dermatitis and a rare inflammatory condition and has product candidates in development in other areas of high unmet medical need, including rheumatoid arthritis, asthma, pain, cancer and infectious diseases. Summary: This position requires strong scientific and extensive publication management experience. Work with company scientists and other internal stakeholders, study investigators and authors, external pharmaceutical company partners, and medical communication agencies in leading cross-functional publication teams for one or more therapeutic areas for the development of scientific publication plans (covering research manuscripts and conference presentations) and their execution. Demonstrated ability to work with stakeholders in a pharma company setting and manage publication vendors is required. Ability to write manuscripts is a must. Responsibilities: Lead cross-functional publication teams (together with other pharma partners) to develop, manage and execute the publication plan of one or more therapeutic areas. This involves the development and submission of clinical manuscripts, abstracts, and scientific meeting presentations with company teams, publication vendors, external collaborators, scientists, and medical experts. Understand the science of the assigned therapeutic areas. Guide and oversee publication vendors, contract writers and editors, draft budgets, and travel to scientific conferences as needed. Write manuscripts, abstracts, posters on behalf of authors. Requirements: At least 6 years in medical communications or publications management, of which 2-3 years must have been spent in independently leading cross-functional publication teams to develop and execute therapeutic area-specific publication plans. Some or all of this experience must be from a pharmaceutical company; additional experience in a medical communication agency is a plus. Experience in medical writing required. Quickly develop a firm scientific understanding of the therapeutic area(s) covered; should possess an understanding of clinical study design, statistics, and pharmaceutical research and development. Familiarity with statistical analysis plans and clinical study reports. Must be able to write manuscripts, abstracts, posters on behalf of authors. Oversee publication vendors, contract writers and editors, drafting publication budgets. Prior use of publication software (e.g., Datavision) a plus. Excellent knowledge of and compliance with Good publication practices, ICMJE guidelines, CONSORT, Sunshine Act Strong project management skills, with demonstrated ability to work on multiple projects efficiently are important. Excellent written and oral communication skills are required. Additionally, exemplary professional interaction with internal stakeholders and external authors is expected.

Known for its scientific and operational excellence, Regeneron is a leading science-based biopharmaceutical company that discovers, invents, develops, manufactures, and commercializes medicines for the treatment of serious medical conditions. Regeneron commercializes medicines for eye diseases, high LDL-cholesterol, atopic dermatitis and a rare inflammatory condition and has product candidates in development in other areas of high unmet medical need, including rheumatoid arthritis, asthma, pain, cancer and infectious diseases. Summary Regeneron is currently seeking a talented and motivated Automation Associate to join the Automation Technologies group. The Automation Associate will be responsible for implementation and execution of new and current automated devices and integrated systems. In addition, this will include programming new methods and updates, software and driver development, and design and creation of custom parts and devices to support automation. Successful candidates will be well versed in the latest automated technologies, have a hands-on aptitude and be willing to work in fast paced team-oriented environment. Preferred experience should include: -Programming experience in C#, Python, Python, Ruby, C, C++, VB etc. -3D Modeling and 3D Printer usage experience -Experience with firmware, microcontrollers, circuit design -Programming experience with automated liquid handlers such as Hamilton STAR, Beckman Biomek FX, Tecan Fluent -Experience and knowledge of various devices necessary for research laboratory integrations Responsibilities • Develop custom software and drivers for automated systems and devices • Design, model, and 3D print custom parts, labware, and fixtures to support R&D • Performs activities related to design, commissioning, performance improvement, and troubleshooting of automation technologies • Provides technical and automation operational support to Research and Development facilities • Implements software/hardware changes and upgrades, understands impact of actions to R&D • Implements modification/change to established procedures and protocols • Programs liquid handlers and supporting devices • Capable of troubleshooting and demonstrates knowledge of instrumentation and controls • Work with scientists to develop novel approaches through automation • Train users to operate new equipment and extend an ongoing support Requirements B.S or M.S. in Science/Engineering or related field with relevant automation experience. Knowledge of liquid handlers and integrated systems. General molecular biology and cell culture skills are a plus. Strong communication and organizational skills. Hands-on experiences and trouble-shooting proficiency of Automation equipment. This is an opportunity to join our select team that is already leading the way in the Pharmaceutical/Biotech industry. Apply today and learn more about Regeneron's unwavering commitment to combining good science & good business. #LI-GP1 LI-GP1 To all agencies: Please, no phone calls or emails to any employee of Regeneron about this opening. All resumes submitted by search firms/employment agencies to any employee at Regeneron via-email, the internet or in any form and/or method will be deemed the sole property of Regeneron, unless such search firms/employment agencies were engaged by Regeneron for this position and a valid agreement with Regeneron is in place. In the event a candidate who was submitted outside of the Regeneron agency engagement process is hired, no fee or payment of any kind will be paid. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, sexual orientation, gender identity, disability status, protected veteran status, or any other characteristic protected by law.

Known for its scientific and operational excellence, Regeneron is a leading science-based biopharmaceutical company that discovers, invents, develops, manufactures, and commercializes medicines for the treatment of serious medical conditions. Regeneron commercializes medicines for eye diseases, high LDL-cholesterol, atopic dermatitis and a rare inflammatory condition and has product candidates in development in other areas of high unmet medical need, including rheumatoid arthritis, asthma, pain, cancer and infectious diseases. Summary: Act as subject matter expert (SME) for the administration of Regeneron's LMS (SumTotal). Train and support Business Administrators of SumTotal (ST). Improve ST usability and efficiency. Responsibilities: Perform advanced SumTotal administration functions including but not limited to: *Create ad-hoc reports *Create audiences *Appropriately remove activities *Troubleshoot user & administrative issues *Enable, inactivate and modify notifications *Populate and test the creation of the TMU template files Instruct administrators on the detailed requirements and risks associated with developing various SumTotal activity structures in order to maximize learner experience and business efficiencies: *ILTs *Curriculums *Fulfillment links *Versionals *Certifications Teach/instruct/explain SumTotal system Develop clear documentation of procedures, processes and best practices. Manage small to medium scale LMS enhancement projects Create quality assurance (QA) test scripts and conduct QA tests of training prior to course / new feature deployment Stay current on SumTotal features and functionality by reviewing SumTotal release notes and participating in release webinars, etc Manage and resolve daily LMS help tickets Requirements: o Strong written and verbal communication skills o Strong organization and prioritization skills o Strong interpersonal and customer service skills o Minimum BS degree (or 10 years equivalent experience) o Minimum 5 years' experience managing SumTotal LMS • Hands-on knowledge of SCORM standard and authoring techniques including Captivate or Storyline experience • Experience managing eLearning vendors • Experience with Workday HCM a plus SumTotal, MS Office, SharePoint Minimum Years of Experience: • Bachelor's Degree strongly preferred • Minimum 7 - 9 years of relevant experience This is an opportunity to join our select team that is already leading the way in the Pharmaceutical/Biotech industry. Apply today and learn more about Regeneron's unwavering commitment to combining good science & good business. To all agencies: Please, no phone calls or emails to any employee of Regeneron about this opening. All resumes submitted by search firms/employment agencies to any employee at Regeneron via-email, the internet or in any form and/or method will be deemed the sole property of Regeneron, unless such search firms/employment agencies were engaged by Regeneron for this position and a valid agreement with Regeneron is in place. In the event a candidate who was submitted outside of the Regeneron agency engagement process is hired, no fee or payment of any kind will be paid. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, sexual orientation, gender identity, disability status, protected veteran status, or any other characteristic protected by law.

Known for its scientific and operational excellence, Regeneron is a leading science-based biopharmaceutical company that discovers, invents, develops, manufactures, and commercializes medicines for the treatment of serious medical conditions. Regeneron commercializes medicines for eye diseases, high LDL-cholesterol, atopic dermatitis and a rare inflammatory condition and has product candidates in development in other areas of high unmet medical need, including rheumatoid arthritis, asthma, pain, cancer and infectious diseases. Summary: The Senior Sourcing Manager will be responsible to support and assist in the development of the Category Management strategy by gathering and anticipating business unit supply needs and specifications for the Commercial organization. She/he works collaboratively with the Category Manager and business unit stakeholders to commercially & competitively assess the local supply base's capabilities and qualifications for Regeneron's interests. The Senior Sourcing Manager owns the local supplier relationship and manages ongoing performance and service delivery. She/he must have demonstrated capability to proactively manage a supply base and maximize value, minimize risk, and ensure quality & cost effectiveness. SCOPE: Local supply markets Responsibilities: • Leads and/or works with others to solve issues of diverse scope where analysis requires an understanding of current business trends • Uses sophisticated analytical thought to exercise judgement and identify innovative solutions • Requires broad understanding of the processes, procedures and systems and is able to use that knowledge to improve efficiency and produce high quality work on problems with cross functional impact • Responsible for specific local contractual agreements, works with internal legal department, and drives any changes that are critical to Regeneron's interest • Develops and executes sourcing strategies for respective area of spend responsibility to optimize value • Solicits and analyzes requests for proposals, negotiates contracts, and ensure contract objectives are delivered (savings, SLAs, etc.); ensures compliance with local pricing agreements and internal policies/procedures • Manages local vendor/supplier relationships and ensures performance and accountability are tracked/improved • Develops and manages program policies and procedures ensuring compliance with Company guidelines, related laws and governmental guidelines • Develops and executes local market procurement related programs to optimize value • Informs and influences decision making at the management level • Manages local supplier integration plans with internal clients for all goods and services for consumption by internal stakeholders, business unit or function • Identifies local supply market projects to apply sourcing and procurement methodologies • Conducts local supplier relationship management activities as guided by the Supplier Management Program to achieve continuous improvement goals • Coaches and develops proficiency in procurement technical skills among direct reports (if applicable), peers, and junior team members Requirements: Education • Bachelor's plus 10 years of relevant, progressive experience within procurement, to preferrably include 7 years directly in sourcing Pharma/Biotech. Or • Master's plus 7 years of relevant, progressive experience within procurement, to preferrably include 7 years directly in sourcing within Pharma/Biotech. • CPSM/CPM preferred Experience • Working knowledge with Sourcing Contracting, ERP, eRFX systems preferred. (Oracle, Zycus, GEP, Ariba, Other) • Ability to leverage standard business applications for communicating, presenting and analyzing (Word, Excel, Powerpoint) • Previous leadership experience preferred. • Advanced level proficiency using negotiations skills • Cost modeling knowledge • Excellent verbal and written skills • Ability to formulate high level presentations and business cases • Ability to build consensus, teamwork, and creativity within a collaborative team with limited supervision • Program management experience and project management experience required This is an opportunity to join our select team that is already leading the way in the Pharmaceutical/Biotech industry. Apply today and learn more about Regeneron's unwavering commitment to combining good science & good business. To all agencies: Please, no phone calls or emails to any employee of Regeneron about this opening. All resumes submitted by search firms/employment agencies to any employee at Regeneron via-email, the internet or in any form and/or method will be deemed the sole property of Regeneron, unless such search firms/employment agencies were engaged by Regeneron for this position and a valid agreement with Regeneron is in place. In the event a candidate who was submitted outside of the Regeneron agency engagement process is hired, no fee or payment of any kind will be paid. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, sexual orientation, gender identity, disability status, protected veteran status, or any other characteristic protected by law.

Known for its scientific and operational excellence, Regeneron is a leading science-based biopharmaceutical company that discovers, invents, develops, manufactures, and commercializes medicines for the treatment of serious medical conditions. Regeneron commercializes medicines for eye diseases, high LDL-cholesterol, atopic dermatitis and a rare inflammatory condition and has product candidates in development in other areas of high unmet medical need, including rheumatoid arthritis, asthma, pain, cancer and infectious diseases. Summary: The Program Finance Sr. Financial Analyst is the dedicated "Product CFO" for development projects within assigned therapeutic areas, providing value-add analyses and interpretation for relevant stakeholders including Senior Management, Program Direction/Program Management, Development teams, and external collaborators. The incumbent will implement best practices to drive efficient management across their therapeutic areas; develop annual financial operating plans and deliver other financial reviews as required. The incumbent maintains a solid command of all aspects of projects; can readily identify and update assumptions incorporated in forecasts/budgets to reflect the latest information; and works closely with functional finance subject matter experts to test all assumptions. He/she uses a repertoire of financial analyses to support decision making and to validate that programs budgets are based on "realistic" assumptions. Responsibilities: • Own the Financial Reporting and Analysis for programs (preclinical, clinical, manufacturing) within assigned therapeutic areas including monthly actuals reporting, quarterly forecast analysis and deck preparation to effectively communicate the status of each project's/program's financial execution and variance to plan/forecast • Own deliverables for collaboration programs within their Therapeutic Areas by working closely with Program Alliance Finance and other team members • Analyze actual costs against budgets, track commitments and efforts with emphasis on performance against plans and collaboration agreements to ensure effective and accurate program cost reporting. • Lead the preparation and analysis of the Annual Operating Plan, and quarterly forecast updates for assigned programs • Provide insightful analysis of program level business results to senior management and perform ad-hoc analyses that lead to problem solving and sound business recommendations • Work with cross-functional teams, subject matter experts and external collaboration partners to manage and communicate P&L and Balance Sheet implications; monthly and quarterly activities include working with the Accounting group to ensure accuracy and completeness of journal entries • Work closely with the Analyst responsible for the Therapeutic Area on program workbook maintenance, accounting reconciliations, and internal cost management and story-telling • Ad-hoc projects and analyses as needed Requirements: • Strong verbal and written communication skills to effectively interact with all levels of business partners and management • Demonstrated ability to translate financial information to non-finance audiences, including senior management levels • 3-5+ years of (preferably post MBA) experience with forecasting, budgeting and/or business partnering ideally in a science or research driven environment • Excellent analytical skills and the ability to translate analytical findings into actionable solutions and processes • Bachelors degree in a scientific or quantitative field combined with top tier MBA a significant plus • Demonstrated ability to manage multiple priorities in fast paced environment • Proficiency in Excel. Experience with Pivot tables and/or Hyperion a plus. This is an opportunity to join our select team that is already leading the way in the Pharmaceutical/Biotech industry. Apply today and learn more about Regeneron's unwavering commitment to combining good science & good business. To all agencies: Please, no phone calls or emails to any employee of Regeneron about this opening. All resumes submitted by search firms/employment agencies to any employee at Regeneron via-email, the internet or in any form and/or method will be deemed the sole property of Regeneron, unless such search firms/employment agencies were engaged by Regeneron for this position and a valid agreement with Regeneron is in place. In the event a candidate who was submitted outside of the Regeneron agency engagement process is hired, no fee or payment of any kind will be paid. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, sexual orientation, gender identity, disability status, protected veteran status, or any other characteristic protected by law.

Known for its scientific and operational excellence, Regeneron is a leading science-based biopharmaceutical company that discovers, invents, develops, manufactures, and commercializes medicines for the treatment of serious medical conditions. Regeneron commercializes medicines for eye diseases, high LDL-cholesterol, atopic dermatitis and a rare inflammatory condition and has product candidates in development in other areas of high unmet medical need, including rheumatoid arthritis, asthma, pain, cancer and infectious diseases. Summary: In Research and Development IT, we deliver complex enterprise systems to help Research Scientists at Regeneron solve their toughest business problems. We bring together multi-disciplinary, highly-skilled technical teams to deliver high-quality technical solutions and services that deliver business value. The Senior Manager with Open-source and distributed computing similar to Swift, Java, nodejs, Angular, React is a key role on the team, enabling science by leading the architecture, design, implementation, testing, deployment, and maintenance standards of new and existing custom-built applications that add demonstrable value to the scientific operations of Research & Development at Regeneron. Our stack currently includes Java, Ruby on Rails, React, AWS, Docker, Postgres, MongoDB, and some legacy technologies and tools. The Senior Manager will be comfortable with this technology landscape but will also bring a broad understanding of modern technologies, architectural principles and design patterns, and will formulate a technology roadmap that aligns with business priorities, scales for the future, and disrupts when necessary to continually improve and deliver value. Responsibilities: The role you will play includes: • Hands-on technologist with skills to lead and collaborate with the engineering team • Working as a technology lead with both internal and external stake holder • Modernizing the legacy technologies across scientific application landscape • Collaborating with and influencing others to build the next generation of applications to support the ever-evolving needs of Regeneron's scientists • Acting as an expert technical resource for enterprise architecture, solution architecture, software development, and testing • Defining and driving adoption of best practices in code health, testing, and maintainability across Regeneron • Maintaining strong expertise and knowledge of current and emerging technologies and products; evaluating and implementing new technologies, development frameworks, and languages • Mentoring on approach and execution of solutions, coaching on technologies, and establishing a team-wide comprehension of solution capabilities and direction Requirements: Skills and expertise you will bring to the table include: • 7+ years' experience in systems implementations with a focus on custom web application development • Proven ability to adapt to new languages, frameworks, technologies as the need arises; previous experience in a role selecting, adopting, and using technology that makes business sense, is supportable, and scalable • Significant software development and infrastructure architecture experience in designing and architecting enterprise web applications • Experience leading and inspiring software development teams • Demonstrable skill in collaborating with other IT teams, vendor partners, internal collaborators, and architects to deliver solutions; advocacy for a DevOps approach to the software development lifecycle • Solid understanding of the practical application of Agile development methods and leading software development teams in an Agile/Lean/Continuous Delivery environment • Ability to formulate and articulate the technical and political implications of creating and delivering transformative technical solutions in an innovative, high-growth, demanding business area • Experience working directly with senior IT leaders in an advisory role on technical strategies • Interest in and experience mentoring junior developers and driving technical discussions and decisions • Progressive industry experience; Information Technology / Biotechnology / Pharmaceutical preferred This is an opportunity to join our select team that is already leading the way in the Pharmaceutical/Biotech industry. Apply today and learn more about Regeneron's unwavering commitment to combining good science & good business. To all agencies: Please, no phone calls or emails to any employee of Regeneron about this opening. All resumes submitted by search firms/employment agencies to any employee at Regeneron via-email, the internet or in any form and/or method will be deemed the sole property of Regeneron, unless such search firms/employment agencies were engaged by Regeneron for this position and a valid agreement with Regeneron is in place. In the event a candidate who was submitted outside of the Regeneron agency engagement process is hired, no fee or payment of any kind will be paid. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, sexual orientation, gender identity, disability status, protected veteran status, or any other characteristic protected by law.

Known for its scientific and operational excellence, Regeneron is a leading science-based biopharmaceutical company that discovers, invents, develops, manufactures, and commercializes medicines for the treatment of serious medical conditions. Regeneron commercializes medicines for eye diseases, high LDL-cholesterol, atopic dermatitis and a rare inflammatory condition and has product candidates in development in other areas of high unmet medical need, including rheumatoid arthritis, asthma, pain, cancer and infectious diseases. Summary We are seeking an experienced and motivated Scientist to join the Bispecific group, a multidisciplinary team that designs and evaluates novel bispecific and alternative antibody formats across multiple therapeutic areas. The successful candidate will be responsible for designing, executing and analyzing preclinical in vivo and in vitro/ex vivo experiments to evaluate the efficacy and explore the mechanism of action of immune modulating antibodies to treat cancer. Ideal candidates will possess a deep understanding of immunology principles, and extensive laboratory experience in cellular biology/immunology with a focus or experience on in vivo mouse modeling. Ideal applicants will possess excellent interpersonal and communication skills, as this candidate will be expected to work productively in a collaborative, cross-functional team environment and efficiently present her/his findings to internal multi-disciplinary teams. Responsibilities Design, plan, and independently perform complex in vivo experiments, including establishing novel tumor models in immune compromised and immune competent mice. Design complex flow cytometry (FACS) panels and perform FACS analysis on human and murine cells, tumors, and tissues. Perform a variety of in vitro/ex vivo immune cell-based assays, such as FACS based cytotoxicity and serum/supernatant analyte analysis (ELISA, MSD, CBA). Analyze data using biological and statistical software such as Flowjo, Prism, Excel, and algorithmic tools for high-dimensional cytometry data analysis (tSNE, SPADE, FlowSOM, etc) Document experimental procedures and results in a well-organized fashion; generate experimental reports. Participate in general lab duties of the team Synthesize results across experiments and programs in PowerPoint presentations and present to colleagues and senior management, including clinical and regulatory teams. Collaborate closely with cross-functional teams across the company. #LI-GP1 Requirements PhD + 3+ years post-doctoral or industry experience Strong background in cellular and molecular immunology and/or immuno-oncology; experience with protein therapeutics, such bispecific or novel antibody formats, is desirable Experience with designing and performing all aspects of tumor modeling in mice, including mouse handling, tumor/therapeutic implantation/injection (iv, ip, sc), tumor growth monitoring, and dissection of mouse lymphoid organs and tumors, followed by in vitro processing/purification of tissues/cells. Extensive knowledge and practical experience with advanced flow cytometry including complex panel design for cell surface and intracellular staining, data acquisition and analysis. Experience in cell culture (both primary cells and established cell lines), and the execution of a variety of in vitro/ex vivo immune cell-based assays This position will require the individual to pass a physical before beginning employment. This is an opportunity to join our select team that is already leading the way in the Pharmaceutical/Biotech industry. Apply today and learn more about Regeneron's unwavering commitment to combining good science & good business. To all agencies: Please, no phone calls or emails to any employee of Regeneron about this opening. All resumes submitted by search firms/employment agencies to any employee at Regeneron via-email, the internet or in any form and/or method will be deemed the sole property of Regeneron, unless such search firms/employment agencies were engaged by Regeneron for this position and a valid agreement with Regeneron is in place. In the event a candidate who was submitted outside of the Regeneron agency engagement process is hired, no fee or payment of any kind will be paid. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, sexual orientation, gender identity, disability status, protected veteran status, or any other characteristic protected by law.

Known for its scientific and operational excellence, Regeneron is a leading science-based biopharmaceutical company that discovers, invents, develops, manufactures, and commercializes medicines for the treatment of serious medical conditions. Regeneron commercializes medicines for eye diseases, high LDL-cholesterol, atopic dermatitis and a rare inflammatory condition and has product candidates in development in other areas of high unmet medical need, including rheumatoid arthritis, asthma, pain, cancer and infectious diseases. Summary: Provide support on all areas of compensation in regards to Regeneron's base, bonus, long-term incentive programs. Primary focus of this role will be to support the compensation team on Workday implementation, and in specific the Global Job Architecture framework and Job Catalog project. Responsibilities: • Contribute to the documentation of process design and support the implementation of compensation program elements in Workday. • Work with the compensation team on the development of job functions and families. Work with project team to review and refine current job level framework, job title nomenclature and rationalization, employee mapping, pay structure review and job documentation. • Drafts sample job descriptions and assists managers and staff members in job description preparation. • Work with the compensation team on any other related project including compensation program analysis, budgeting, and implementation process. • Provide ad-hoc metric analytics as requested. Requirements: • Knowledge of government regulations as they apply to compensation programs. • Knowledge of job architecture framework and job evaluation • Experience in market pay analysis • Strong analytical, computer and communication skills. • Strong understanding of Microsoft Excel application. • Experience with an HRM, such as Workday, preferred Minimum Years of Experience: • Bachelor's degree with 3-4 years compensation experience preferably in the Pharmaceutical or Biotech industry. CCP certification a plus. Experience with an HRM, such as Workday, preferred This is an opportunity to join our select team that is already leading the way in the Pharmaceutical/Biotech industry. Apply today and learn more about Regeneron's unwavering commitment to combining good science & good business. To all agencies: Please, no phone calls or emails to any employee of Regeneron about this opening. All resumes submitted by search firms/employment agencies to any employee at Regeneron via-email, the internet or in any form and/or method will be deemed the sole property of Regeneron, unless such search firms/employment agencies were engaged by Regeneron for this position and a valid agreement with Regeneron is in place. In the event a candidate who was submitted outside of the Regeneron agency engagement process is hired, no fee or payment of any kind will be paid. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, sexual orientation, gender identity, disability status, protected veteran status, or any other characteristic protected by law.

Known for its scientific and operational excellence, Regeneron is a leading science-based biopharmaceutical company that discovers, invents, develops, manufactures, and commercializes medicines for the treatment of serious medical conditions. Regeneron commercializes medicines for eye diseases, high LDL-cholesterol, atopic dermatitis and a rare inflammatory condition and has product candidates in development in other areas of high unmet medical need, including rheumatoid arthritis, asthma, pain, cancer and infectious diseases. Summary We are seeking a Scientist with Ph.D. degree to join the Analytical Chemistry group of Regeneron Pharmaceutical Inc. located at Tarrytown, NY. This role will work in a state-of-the-art mass spectrometry lab and provide biochemical characterization of therapeutic protein drug candidates to support different stages of drug development, from early-stage candidate selections to late-stage regulatory submissions. This role will also have opportunities to develop innovative mass spectrometry technologies to support Regeneron R&D programs in the context of multidisciplinary project teams. Responsibilities • Independently develop and apply state-of-the-art mass spectrometry and its related technologies for the analytical characterization of therapeutic protein drug candidates and/or products, including monoclonal and bispecific antibodies, to support different drug development activities at all stages. • Work independently for designing experiments, drafting protocols, executing experiments, performing data analysis, documenting work in electronic notebooks and generating study reports. • Work closely with multi-functional project teams, including but not limited to research, formulation, process development, pharmacokinetic/pharmacodynamics, etc.; provide high quality analytical data and present results at group, department, and cross-functional team meetings. • Keep abreast of identifying the opportunities to improve existing or develop innovative analytical methods (e.g. novel MS or LC-MS/MS methods) to better support therapeutic protein characterization and drug development and publish in peer-reviewed journals. • Other responsibilities may include but are not limited to performing analytical characterization for therapeutic antibody development and regulatory submissions and authoring characterization sections of regulatory submissions (e.g. INDs, comparability, and BLAs). Requirements • Ph.D. in Analytical Chemistry, Chemistry, Biochemistry, Pharmaceutical Science, Chemical or Biomedical Engineering (or related discipline) with a concentration on mass spectrometry and its related fields for protein characterization, proteomics, and PTM analysis, as well as a proven track record of publications in the fields. Post-doctoral and/or biotech/biopharma industry experience (0-5 years) is preferred. • Proficient in developing and performing mass spectrometry and UPLC as well as the associated applications for protein characterization. • Ability in programming, automation, DoE and/or protein modeling is preferred. • Willing to work in a dynamic, fast-paced environment and be capable of handling multiple tasks while meeting timelines and adapting to changing priorities. • Ability to support management and to work in cross functional teams. • Must have enthusiasm in science and technology and is highly self-motivated and eager to learn. • Must have excellent written and verbal communication skills. This is an opportunity to join our select team that is already leading the way in the Pharmaceutical/Biotech industry. Apply today and learn more about Regeneron's unwavering commitment to combining good science & good business. To all agencies: Please, no phone calls or emails to any employee of Regeneron about this opening. All resumes submitted by search firms/employment agencies to any employee at Regeneron via-email, the internet or in any form and/or method will be deemed the sole property of Regeneron, unless such search firms/employment agencies were engaged by Regeneron for this position and a valid agreement with Regeneron is in place. In the event a candidate who was submitted outside of the Regeneron agency engagement process is hired, no fee or payment of any kind will be paid. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, sexual orientation, gender identity, disability status, protected veteran status, or any other characteristic protected by law.

Known for its scientific and operational excellence, Regeneron is a leading science-based biopharmaceutical company that discovers, invents, develops, manufactures, and commercializes medicines for the treatment of serious medical conditions. Regeneron commercializes medicines for eye diseases, high LDL-cholesterol, atopic dermatitis and a rare inflammatory condition and has product candidates in development in other areas of high unmet medical need, including rheumatoid arthritis, asthma, pain, cancer and infectious diseases. Summary: Using scientific knowledge and project management techniques, the Research Program Management (RPM) team is seeking the right candidate to support the operational and scientific activities within the Inflammation and Immune-Disease team. The Project Associate role provides scientific expertise and interpersonal skills required to advance a project / program through key milestones and objectives, providing effective operational guidance to cross functional research and technology project / program teams. Responsibilities: • Research Project Management: Provides overall support to a functional area / department, working group or project team which may include the creation of templates, working and best practices, meeting logistics / management and developing tracking, training and monitoring tools. • Communication: Ensures effective, accurate and timely communication within a department, working group or project team. Develops good working relationships with department leaders, line managers and individual stakeholders, both within and outside the department. • Collaborations: Supports and coordinate tracking, information sharing and communications within Regeneron and between Regeneron and collaborators. • Project Planning and Tracking: Uses project management techniques to identify, develop and maintain planning tools for assigned projects including coordination of tasks across functional areas, working groups or project teams. • Data Management: Supports the development, implementation and administration of tracking tools, workflows and processes to support a department and/or project. Updates information into shared databases (e.g SharePoint); maintains and updates best practices. • Process Improvement: Assists with defining and documenting working / best practices for a function or project team. • Problem Solving: Identifies opportunities and develops tools and mechanisms for monitoring progress and routine problem solving within a functional area, working group or project team. Requirements: This position requires a minimum of a BS / MS / PhD and 2-3 years of research or project management experience in a scientific discipline or the drug discovery / development industry. Advanced degree (e.g. PhD) and/or experience with Program Management is a plus. Additional requirements include: • The successful candidate demonstrates excellent written, verbal and interpersonal communication skills, is action oriented, organized and has basic knowledge of project management techniques and concepts as they apply to the life sciences. • Is able to use previous hands-on experience and technical knowledge in areas including molecular biology, protein biochemistry or purification, cell biology, immunology (or related research areas) to effectively support cross-functional project teams. • Is a quick learner and able to analyze scientific literature and data • Handles multiple projects and priorities with excellent time management skills (both project and self). • Is able to interact with team members and stakeholders with tact and diplomacy, with the ability to lead. • Demonstrates proficiency in Microsoft office suite. General knowledge with shared work environments and scientific programs and databases (eg. pubmed, uniprot, Macvector, BLAST etc) is a plus. It is strongly recommended that you include a cover letter stating your interest in this role. This is an opportunity to join our select team that is already leading the way in the Pharmaceutical/Biotech industry. Apply today and learn more about Regeneron's unwavering commitment to combining good science & good business. To all agencies: Please, no phone calls or emails to any employee of Regeneron about this opening. All resumes submitted by search firms/employment agencies to any employee at Regeneron via-email, the internet or in any form and/or method will be deemed the sole property of Regeneron, unless such search firms/employment agencies were engaged by Regeneron for this position and a valid agreement with Regeneron is in place. In the event a candidate who was submitted outside of the Regeneron agency engagement process is hired, no fee or payment of any kind will be paid. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, sexual orientation, gender identity, disability status, protected veteran status, or any other characteristic protected by law.

Known for its scientific and operational excellence, Regeneron is a leading science-based biopharmaceutical company that discovers, invents, develops, manufactures, and commercializes medicines for the treatment of serious medical conditions. Regeneron commercializes medicines for eye diseases, high LDL-cholesterol, atopic dermatitis and a rare inflammatory condition and has product candidates in development in other areas of high unmet medical need, including rheumatoid arthritis, asthma, pain, cancer and infectious diseases. Summary: Provides scientific exchange and collaboration with therapeutic area opinion leaders on disease and product information as well as research initiatives. Participates in the development and the management of company and investigator sponsored clinical trials. Presents scientific and clinical data in response to requests for information related to study indications and disease state awareness to opinion leaders, practitioners, investigators, research coordinators, site personnel and internal study stakeholders. Responsibilities: Provides scientific exchange and collaboration with therapeutic area opinion leaders on disease and product information as well as research initiatives Participates in the development and the management of company and investigator sponsored clinical trials including: Concept proposals Protocol development and review Site selection Investigator identification Act as a scientific resource for area healthcare professionals within the surrounding trial site community Consults with physicians, pharmacists and other medical professionals to refer appropriate patients to Clinical Trial sites and review clinical practice topics as requested by the customer Identifies gaps in research needs of company and create opportunities for the organization to fill those gaps by collaborating with potential and existing investigators Assists with management of clinical data through support of abstracts, posters, presentations and manuscript development to ensure rapid and accurate communication of scientific and clinical results Presents scientific and clinical data in response to requests for information related to study indications and disease state awareness to opinion leaders, practitioners, investigators, research coordinators, site personnel and internal study stakeholders Performs disease management consultations and provides education for the therapeutic area with identified practitioners, payers and researchers Ensures company policies, principles and financial controls are maintained with integrity and professionalism being displayed internally and externally Appropriately engages healthcare professionals and attends medical conferences to collect and report relevant competitive intelligence Collaborates with Clinical and other study staff to execute plans and strategies established by Medical Affairs Maintains a list of primary healthcare practitioner/opinion leader/investigator targets and associated plans of action Requirements: Education: PhD, PharmD, MD or DVM, Doctor of Veterinary Medicine Experience: 3-5 years Healthcare professional possessing therapeutic experience and/or trial recruitment experience Requires two to five years of relevant experience in a pharmaceutical industry or clinical setting such as drug information, disease management programs or clinical pharmacy/medicine This is an opportunity to join our select team that is already leading the way in the Pharmaceutical/Biotech industry. Apply today and learn more about Regeneron's unwavering commitment to combining good science & good business. To all agencies: Please, no phone calls or emails to any employee of Regeneron about this opening. All resumes submitted by search firms/employment agencies to any employee at Regeneron via-email, the internet or in any form and/or method will be deemed the sole property of Regeneron, unless such search firms/employment agencies were engaged by Regeneron for this position and a valid agreement with Regeneron is in place. In the event a candidate who was submitted outside of the Regeneron agency engagement process is hired, no fee or payment of any kind will be paid. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, sexual orientation, gender identity, disability status, protected veteran status, or any other characteristic protected by law.

Known for its scientific and operational excellence, Regeneron is a leading science-based biopharmaceutical company that discovers, invents, develops, manufactures, and commercializes medicines for the treatment of serious medical conditions. Regeneron commercializes medicines for eye diseases, high LDL-cholesterol, atopic dermatitis and a rare inflammatory condition and has product candidates in development in other areas of high unmet medical need, including rheumatoid arthritis, asthma, pain, cancer and infectious diseases. Summary: Provides scientific exchange and collaboration with therapeutic area opinion leaders on disease and product information as well as research initiatives. Participates in the development and the management of company and investigator sponsored clinical trials. Presents scientific and clinical data in response to requests for information related to study indications and disease state awareness to opinion leaders, practitioners, investigators, research coordinators, site personnel and internal study stakeholders. Responsibilities: Provides scientific exchange and collaboration with therapeutic area opinion leaders on disease and product information as well as research initiatives Participates in the development and the management of company and investigator sponsored clinical trials including: Concept proposals Protocol development and review Site selection Investigator identification Act as a scientific resource for area healthcare professionals within the surrounding trial site community Consults with physicians, pharmacists and other medical professionals to refer appropriate patients to Clinical Trial sites and review clinical practice topics as requested by the customer Identifies gaps in research needs of company and create opportunities for the organization to fill those gaps by collaborating with potential and existing investigators Assists with management of clinical data through support of abstracts, posters, presentations and manuscript development to ensure rapid and accurate communication of scientific and clinical results Presents scientific and clinical data in response to requests for information related to study indications and disease state awareness to opinion leaders, practitioners, investigators, research coordinators, site personnel and internal study stakeholders Performs disease management consultations and provides education for the therapeutic area with identified practitioners, payers and researchers Ensures company policies, principles and financial controls are maintained with integrity and professionalism being displayed internally and externally Appropriately engages healthcare professionals and attends medical conferences to collect and report relevant competitive intelligence Collaborates with Clinical and other study staff to execute plans and strategies established by Medical Affairs Maintains a list of primary healthcare practitioner/opinion leader/investigator targets and associated plans of action Requirements: Education: PhD, PharmD, MD or DVM, Doctor of Veterinary Medicine Experience: 3-5 years Healthcare professional possessing therapeutic experience and/or trial recruitment experience Requires two to five years of relevant experience in a pharmaceutical industry or clinical setting such as drug information, disease management programs or clinical pharmacy/medicine This is an opportunity to join our select team that is already leading the way in the Pharmaceutical/Biotech industry. Apply today and learn more about Regeneron's unwavering commitment to combining good science & good business. To all agencies: Please, no phone calls or emails to any employee of Regeneron about this opening. All resumes submitted by search firms/employment agencies to any employee at Regeneron via-email, the internet or in any form and/or method will be deemed the sole property of Regeneron, unless such search firms/employment agencies were engaged by Regeneron for this position and a valid agreement with Regeneron is in place. In the event a candidate who was submitted outside of the Regeneron agency engagement process is hired, no fee or payment of any kind will be paid. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, sexual orientation, gender identity, disability status, protected veteran status, or any other characteristic protected by law.

Known for its scientific and operational excellence, Regeneron is a leading science-based biopharmaceutical company that discovers, invents, develops, manufactures, and commercializes medicines for the treatment of serious medical conditions. Regeneron commercializes medicines for eye diseases, high LDL-cholesterol, atopic dermatitis and a rare inflammatory condition and has product candidates in development in other areas of high unmet medical need, including rheumatoid arthritis, asthma, pain, cancer and infectious diseases. Summary: We are seeking a motivated Scientist with an advanced degree to join the Ophthalmology group for ocular immune and inflammatory diseases. This position will be part of a group responsible for studying pathogenic mechanisms in ocular immune diseases, the identification and validation of drug targets, and for the creation and testing of biologically based therapeutic agents against these targets. This position will work on in vitro and in vivo ocular inflammatory models for the group. This individual will be responsible for the design and execution of biological experiments necessary to develop animal models and deliver experimental therapeutic candidates. This individual will help evsluate therapeutic candidates with In Vitro and In Vivo experiments, and provide in-house technical expertise for interacting with external collaborators on research projects. The ideal candidate will be hardworking, flexible, innovative and able to function effectively in a fast-paced environment. They will also have excellent communication skills and be able to work well in a team. The preferred candidate will have at least 5 years of laboratory experience. Responsibilities: Design and perform cell culture using primary cell culture and cell lines Design and perform experiments in cellular and in vivo ocular immune and inflammatory disease models Collect and prepare tissue for histological or biochemical analyses Cut and stain ocular tissues, perform microscopy & image analysis Design and Perform cell culture assays for in vitro drug testing and screening Perform data analysis and prepare study report, and laboratory management duties Requirements: This position requires advanced degree, PhD and/or MD with at least 2 years post-doctoral experience. Experience with molecular biology and biochemistry techniques (preparation of cell/tissue for DNA/RNA/protein analysis, ELISA, Western blots, IHC, imaging) Five years of experience working with in vivo ocular immunology or inflammatory animal models preferred, experience with rodent ocular disease models highly desired. Strong organization and communication skills. This position will require the individual to pass a physical before beginning employment. This is an opportunity to join our select team that is already leading the way in the Pharmaceutical/Biotech industry. Apply today and learn more about Regeneron's unwavering commitment to combining good science & good business. To all agencies: Please, no phone calls or emails to any employee of Regeneron about this opening. All resumes submitted by search firms/employment agencies to any employee at Regeneron via-email, the internet or in any form and/or method will be deemed the sole property of Regeneron, unless such search firms/employment agencies were engaged by Regeneron for this position and a valid agreement with Regeneron is in place. In the event a candidate who was submitted outside of the Regeneron agency engagement process is hired, no fee or payment of any kind will be paid. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, sexual orientation, gender identity, disability status, protected veteran status, or any other characteristic protected by law. 2 years post-doctoral work preferred This is an opportunity to join our select team that is already leading the way in the Pharmaceutical/Biotech industry. Apply today and learn more about Regeneron's unwavering commitment to combining good science & good business. To all agencies: Please, no phone calls or emails to any employee of Regeneron about this opening. All resumes submitted by search firms/employment agencies to any employee at Regeneron via-email, the internet or in any form and/or method will be deemed the sole property of Regeneron, unless such search firms/employment agencies were engaged by Regeneron for this position and a valid agreement with Regeneron is in place. In the event a candidate who was submitted outside of the Regeneron agency engagement process is hired, no fee or payment of any kind will be paid. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, sexual orientation, gender identity, disability status, protected veteran status, or any other characteristic protected by law.

Known for its scientific and operational excellence, Regeneron is a leading science-based biopharmaceutical company that discovers, invents, develops, manufactures, and commercializes medicines for the treatment of serious medical conditions. Regeneron commercializes medicines for eye diseases, high LDL-cholesterol, atopic dermatitis and a rare inflammatory condition and has product candidates in development in other areas of high unmet medical need, including rheumatoid arthritis, asthma, pain, cancer and infectious diseases. Summary: Provides scientific exchange and collaboration with therapeutic area opinion leaders on disease and product information as well as research initiatives. Participates in the development and the management of company and investigator sponsored clinical trials. Presents scientific and clinical data in response to requests for information related to study indications and disease state awareness to opinion leaders, practitioners, investigators, research coordinators, site personnel and internal study stakeholders. Responsibilities: Provides scientific exchange and collaboration with therapeutic area opinion leaders on disease and product information as well as research initiatives Participates in the development and the management of company and investigator sponsored clinical trials including: Concept proposals Protocol development and review Site selection Investigator identification Act as a scientific resource for area healthcare professionals within the surrounding trial site community Consults with physicians, pharmacists and other medical professionals to refer appropriate patients to Clinical Trial sites and review clinical practice topics as requested by the customer Identifies gaps in research needs of company and create opportunities for the organization to fill those gaps by collaborating with potential and existing investigators Assists with management of clinical data through support of abstracts, posters, presentations and manuscript development to ensure rapid and accurate communication of scientific and clinical results Presents scientific and clinical data in response to requests for information related to study indications and disease state awareness to opinion leaders, practitioners, investigators, research coordinators, site personnel and internal study stakeholders Performs disease management consultations and provides education for the therapeutic area with identified practitioners, payers and researchers Ensures company policies, principles and financial controls are maintained with integrity and professionalism being displayed internally and externally Appropriately engages healthcare professionals and attends medical conferences to collect and report relevant competitive intelligence Collaborates with Clinical and other study staff to execute plans and strategies established by Medical Affairs Maintains a list of primary healthcare practitioner/opinion leader/investigator targets and associated plans of action Requirements: Education: PhD, PharmD, MD or DVM, Doctor of Veterinary Medicine Experience: 3-5 years Healthcare professional possessing therapeutic experience and/or trial recruitment experience Requires two to five years of relevant experience in a pharmaceutical industry or clinical setting such as drug information, disease management programs or clinical pharmacy/medicine This is an opportunity to join our select team that is already leading the way in the Pharmaceutical/Biotech industry. Apply today and learn more about Regeneron's unwavering commitment to combining good science & good business. To all agencies: Please, no phone calls or emails to any employee of Regeneron about this opening. All resumes submitted by search firms/employment agencies to any employee at Regeneron via-email, the internet or in any form and/or method will be deemed the sole property of Regeneron, unless such search firms/employment agencies were engaged by Regeneron for this position and a valid agreement with Regeneron is in place. In the event a candidate who was submitted outside of the Regeneron agency engagement process is hired, no fee or payment of any kind will be paid. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, sexual orientation, gender identity, disability status, protected veteran status, or any other characteristic protected by law.

Known for its scientific and operational excellence, Regeneron is a leading science-based biopharmaceutical company that discovers, invents, develops, manufactures, and commercializes medicines for the treatment of serious medical conditions. Regeneron commercializes medicines for eye diseases, high LDL-cholesterol, atopic dermatitis and a rare inflammatory condition and has product candidates in development in other areas of high unmet medical need, including rheumatoid arthritis, asthma, pain, cancer and infectious diseases. Summary: The Asc Director provides leadership and guidance as the statistical expert on a project team, with minimal direction from Therapeutic Area lead biostatistician. Accountable for all statistical aspects of project studies and submissions, including quality, relevance to regulatory perspective, and scientific validity. May have regional or global management responsibility. In some cases incumbent could serve as technical expert in a particular statistical area or application. Job Duties: • With general guidance from departmental management, assume leadership role for providing statistical support to a project team, including clinical development plans (CDP) and individual protocols. • Work with other BDM members or consultants to develop effective statistical approaches applicable to project. • Interact with the clinical / regulatory functions to define study endpoints and perform relevant sample size calculations. • Learn key clinical and regulatory considerations, ensure that planned statistical methods are applicable, and communicate statistical perspective to clients. • Review statistical analysis plan (SAP) and planned integrated summaries for consistency with overall project objectives. • Produce / coordinate production of statistical summaries, analyses, and related material for submission to regulatory authorities or independent monitoring committees. • Provide guidance, either personally or through a junior member of the statistical team, on definition and documentation of derived variables needed to produce planned TFL. • Assume responsibility for accuracy of derived variables. Effect consistency of data collection and analysis within project. • Oversee execution of the statistical analyses according to the SAP. Advise on relevance and interpretation of proposed ad hoc analyses. • Prepare statistical methods and results sections for CSR and overall summaries. • Provide guidance to the clinical and regulatory teams regarding conclusions and inferences from the project. • Act as company statistical representative at regulatory or external meetings. • Active research interest in area related to clinical trial. • Advises all direct reports about the procedures surrounding retention of data, records, and information for employees in their group. Requirements: Ph.D. in Statistics or related discipline with 8+ years of experience in the experience in the biotechnology, pharmaceutical or health related industry, including some interaction with regulatory bodies and management experience. • Works in a changing and busy environment. • Exercises judgment in interpreting, modifying, and adapting procedures, practices, methods, etc. in accordance with existing policies and standards for application to specific problems or tasks. • Leads by example and manages staff by commitment. • Self-directed and comfortable working in teams with the ability to work and operate independently within a tight deadline environment. • High degree of creativity, latitude and attention to detail required. • Thorough knowledge of pharmaceutical / biotech clinical development • Ability to produce novel and near optimal clinical development plans through integration of statistical thinking with clinical and regulatory considerations • Expertise in at least one therapeutic indication, including in-depth knowledge of key endpoints and regulatory guidelines • Demonstrated knowledge of regulatory guidelines on drug development, NDA submissions, and statistical practices, e.g., CTD guidance, ICH guidelines • Understanding of the drug approval process worldwide • Ability to serve as statistical consultant to company staff • Strong interpersonal and communication skills, experience managing internal team and CROs • Ability to effectively represent Biostatistics and Data Management in multidisciplinary meetings • Strong project management and leadership skills, especially with regard to planning, organizing, tracking, and motivating teams • Ability to anticipate resource needs and participate in planning • SAS, S-Plus/R, Sample size calculation software (e.g., EaSt and Nquery) May report to a Assoc. Director or above. Requires the ability to influence others to achieve results. May manage subordinate supervisors. This is an opportunity to join our select team that is already leading the way in the Pharmaceutical/Biotech industry. Apply today and learn more about Regeneron's unwavering commitment to combining good science & good business. To all agencies: Please, no phone calls or emails to any employee of Regeneron about this opening. All resumes submitted by search firms/employment agencies to any employee at Regeneron via-email, the internet or in any form and/or method will be deemed the sole property of Regeneron, unless such search firms/employment agencies were engaged by Regeneron for this position and a valid agreement with Regeneron is in place. In the event a candidate who was submitted outside of the Regeneron agency engagement process is hired, no fee or payment of any kind will be paid. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, sexual orientation, gender identity, disability status, protected veteran status, or any other characteristic protected by law. Known for its scientific and operational excellence, Regeneron is a leading science-based LMR, #LI-LR1

Known for its scientific and operational excellence, Regeneron is a leading science-based biopharmaceutical company that discovers, invents, develops, manufactures, and commercializes medicines for the treatment of serious medical conditions. Regeneron commercializes medicines for eye diseases, high LDL-cholesterol, atopic dermatitis and a rare inflammatory condition and has product candidates in development in other areas of high unmet medical need, including rheumatoid arthritis, asthma, pain, cancer and infectious diseases. Summary We are seeking candidates for a Scientist position in the Skeletal Diseases Therapeutic Focus Area. The successful candidate will focus on receptor-ligand interactions and signal transduction pathways that affect skeletal homeostasis, iron homeostasis, and rare diseases of the skeleton. Candidates should be versed in Molecular Biology, Biochemistry, and Cell Biology techniques. Although the focus of the work will be primarily in vitro, familiarity with animal models (animal handling, phenotyping) are desirable. Responsibilities The successful candidate is expected to champion research projects in the Skeletal Diseases Therapeutic Focus Area including generation, collecting, presenting and publishing data. They will be expected to work independently as well as part of a team to define research questions and then design a research program focused on answering them, and to communicate ideas and data within the team, as well as in meetings and forums within and outside of Regeneron. The ability to work within interdisciplinary teams in both the discovery and development areas is a necessary attribute for this position. Requirements: • Molecular biology techniques, such as those required for the expression of recombinant proteins and the generation of bioassays. • Bioassay development: Cell culture, cell line production and data generation/analysis. • Biochemistry: Expression, purification, analysis and testing the bioactivity of recombinant proteins. Structural biology: Use imaging and structural biology approaches to study ligand:receptor complexes • Must communicate clearly to coworkers in the laboratory and management. • The ability to generate and analyze data, as well as, interpreting that data to determine next steps. • Flow cytometry, cloning, cell culture is a plus, and a desire to understand the molecular details governing signaling dynamics is a must. • Must be able to work effectively as part of a team. • Should demonstrate creativity and intellectual independence with the ability to lead. • 0 years of experience after a Ph.D. and trained in cell culture and molecular biology is required for this position. This is an opportunity to join our select team that is already leading the way in the Pharmaceutical/Biotech industry. Apply today and learn more about Regeneron's unwavering commitment to combining good science & good business. To all agencies: Please, no phone calls or emails to any employee of Regeneron about this opening. All resumes submitted by search firms/employment agencies to any employee at Regeneron via-email, the internet or in any form and/or method will be deemed the sole property of Regeneron, unless such search firms/employment agencies were engaged by Regeneron for this position and a valid agreement with Regeneron is in place. In the event a candidate who was submitted outside of the Regeneron agency engagement process is hired, no fee or payment of any kind will be paid. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, sexual orientation, gender identity, disability status, protected veteran status, or any other characteristic protected by law.