97 jobs found in Redwood City

Bristol-Myers Squibb is a global Biopharma company committed to a single mission: to discover, develop, and deliver innovative medicines focused on helping millions of patients around the world in disease areas such as oncology, cardiovascular, immunoscience and fibrosis. Join us and make a difference. We hire the best people and provide them with a work environment that places a premium on diversity, integrity, collaboration and personal development. Through a culture of inclusion, we create a better, more productive work environment. We believe that the diverse experiences and perspectives of all our employees help to drive innovation and transformative business results. The Research Investigator will join the Cancer Biology Discovery Research team at Bristol-Myers Squibb in Redwood City, CA. The candidate will be expected to effectively collaborate with scientists in the Tumor Microenvironment Modulation (TME) Thematic Research Center (TRC) to develop novel therapies at the intersection of tumor, immune, and stromal biology. The qualified candidate is a highly motivated, interactive, and creative individual that possesses the ability to work across a highly matrixed environment to advance preclinical drug development programs from target identification/validation through IND enabling activities. The successful candidate will demonstrate clear and professional verbal and written communication, capable of presenting scientific results to multidisciplinary teams and key stakeholders. Responsibilities : Providing expertise in cancer biology/genetic and integrating the current scientific literature and available public dataset into research practice and new target identification Independently designing and executing experiments in both human systems and mouse models to accelerate projects in pre-clinical and clinical development Analyzing and presenting scientific results to internal and external scientists Collaborate with scientists in a dynamic environment to meet timelines and solve problems Maintain accurate electronic laboratory notebooks in a timely fashion and prepare technical reports, summaries, protocols, etc. Qualifications: Ph.D. in Cancer Biology or Cancer Genetic with minimal 2-4 years of relevant industrial experience Knowledge of preclinical drugdevelopment including knowledge of designing assays and flowcharts to identify and optimize drug candidates is required In-depth understanding of the methodologies for in-vitro cellular and biochemical assays, including CRISPR-mediated genome editing, western blotting, immunoprecipitation, reporter assays, siRNA/shRNA knockdown, qPCR, cloning, lentivirus generation and transduction is required Experience with in vivo/ex vivo pharmacology is required. Working knowledge of in-vivo PK, PD and efficacy studies is desirable. Experience in data mining through use of desktop tools/interfaces and public databases (e.g., UCSC genome Browser, CBIO, GTex, Oncoland etc) is required. Proficiency in utilizing software such as Graph Pad, Microsoft office etc. for data analysis and figure generation is required. Ability to mentor more junior scientists and colleagues on best practices in the laboratory would be highly valued. Attention to detail with excellent organizational and record keeping skills is a requirement. Proven interpersonal skills with the ability to interact effectively with people, internally and externally is required. This position is located in Redwood City, CA. There will be less than 10% travel. Bristol-Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees the resources to pursue their goals, both at work and in their personal lives.

Bristol-Myers Squibb is a global Biopharma company committed to a single mission: to discover, develop, and deliver innovative medicines focused on helping millions of patients around the world in disease areas such as oncology, cardiovascular, immunoscience and fibrosis. Join us and make a difference. We hire the best people and provide them with a work environment that places a premium on diversity, integrity, collaboration and personal development. Through a culture of inclusion, we create a better, more productive work environment. We believe that the diverse experiences and perspectives of all our employees help to drive innovation and transformative business results. We are seeking a rigorous, well organized and detail-oriented Research Scientist/Investigator 1 to join the NGS team to perform and develop NGS workflow assays to support immune-oncology drug discovery and translational researches. Candidate will be responsible for establishment, optimization and routine execution of NGS processes including but not limited to single cell or bulk level transcriptomic, genomic and epigenomic sequencing platforms, operating and maintaining NGS equipment, interacting with multiple databases, completing projects in a timely fashion and giving presentations. The candidate should be a problem-solver and able to suggest and to perform assays derived from currently available methods. This position will be located at our state-of-the-art research facility in Redwood City, CA. Responsibilities • Operation of different genomics analysis technologies such as NGS liquid-handler and sequencers, real time PCR, Bioanalyzer for quantification, QC and validation. • Develops, validates, and applies methods for various genomic, epigenomic and transcriptomic sequencing methods. • Processes HT/LT single cell dissociation and nucleic acid isolation from diverse tissue and cell types as needed. • Works with senior and junior members of the team, instrument vendors and IT group to create new workflows that are robust, cost-effective and time efficient. • Accurately and consistently records experimental methods, materials and results in electronic laboratory notebooks. Analyzes data, evaluates results, forms conclusions, and determines future experiments. • Presents findings or project status reviews at internal seminars/meetings. • Establishes and maintains productive relationship with personnel in development; orients and trains other scientists on-site and peers as needed. Requirements • MS or Ph.D in Molecular Biology or other biology background with 4 years of relevant experience and strong knowledge of Molecular Biology. • Strong analytical mindset, detail oriented, and adept at communicating ideas, concepts, and presenting data • Hands-on experience performing qPCR, NGS library prep and biochemistry assay development or other molecular biology methods. • Past experience working in a NGS core facility and/or a company developing assays/products is preferred. • Past experience using bioinformatic pipeline for analysis of NGS data is a plus. • Versatile and adaptable to new methods, technologies and approaches • Proficiency in Microsoft Office applications. • Ability to collaborate in a dynamic and innovative research environment. • Strong verbal and written communication skills. Bristol-Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees the resources to pursue their goals, both at work and in their personal lives.

Oncology is a key therapeutic area for AbbVie, with a portfolio consisting of three marketed products - Imbruvica®, Venclexta™, and Empliciti™ - and a pipeline containing multiple promising new molecules that are being studied in nearly 200 clinical trials in 19 different types of cancer. AbbVie is growing its oncology hub on the West Coast, with three sites in the San Francisco Bay Area (Redwood City, South San Francisco, and Sunnyvale) passionate about the discovery and development of novel oncology therapies. More than 1,000 AbbVie scientists, clinicians, and product developers with strong entrepreneurial roots work across these three sites. They combine their expertise in immuno-oncology, stem cells, and cell-signaling with their knowledge of bispecific antibodies, antibody-drug conjugates (ADCs), and covalent-inhibitor technologies to discover and develop novel cancer treatments. This position will be based at AbbVie Biotherapeutics (ABR), AbbVie's Center of Innovation in Oncology Research and Development, located in Redwood City. ABR R&D efforts are focused on: Immuno-Oncology (I-O): developing therapeutics that activate the immune system to recognize and eliminate cancer cells The Oncology Biologics Department is seeking a highly motivated and experienced in vivo pharmacology scientist to join our Immuno-Oncology Discovery team. In this position, you will participate in the design and execution of high quality in vivo studies supporting the discovery and development of new therapeutics in cancer immunotherapy as part of a multidisciplinary research team in a fast-paced and well supported discovery environment. Key responsibilities: Work with multiple project teams to propose study designs, coordinate logistics and to conduct in vivo studies. Perform all aspects of in vivo studies from receiving animals, to inoculation, randomization using Study Director software, dosing, tumor measurements and pharmacodynamic studies during the study and at necropsy Conduct studies within timelines to help achieve milestone decisions; anticipate potential hurdles and identify alternative strategies to minimize impact to project goals. Maintain accurate and timely records of research, and develop and deliver scientific presentations and reports for internal meetings Work as part of a highly collaborative interdisciplinary team in an integrated and well-supported research laboratory Review, comprehend and follow all SOP's and quality assurance standard pertaining to specific area Bachelor's Degree or equivalent education with typically 5+ years of experience or a Master's Degree (or equivalent education) with 2+ years of experience. Basic: Strong in vivo skills, significant experience with subcutaneous and orthotopic mouse tumor models, including cell inoculations, tumor measurements, and multiple dosing routes. Experience with syngeneic mouse tumor models Experience with mouse autoimmune disease models Experience with mouse autoimmune disease models Strong ex vivo skills such as flow cytometry, ELIspot, ELISA, Luminex, Hemavet highly preferred Demonstrated ability to multi-task on more than one study at a time is highly preferred As this position is part of a dynamic matrixed organization, excellent oral and written communication skills are essential. The ideal candidate has a willingness to adopt new skills as needed. Proficiency with software programs, including Study Director, MS Excel, Powerpoint, Word Preferred: Background in immuno-oncology research Experience with in vitro mammalian cell culture Proficiency with the software programs Prism and Study Director Key Leadership Competencies: Builds strong relationships with peers and cross functionally with partners outside of team to enable higher performance Learns fast, grasps the "essence" and can change course quickly where indicated Raises the bar and is never satisfied with the status quo Creates a learning environment, open to suggestions and experimentation for improvement Embraces the ideas of others, nurtures innovation and manages innovation to reality

Oncology is a key therapeutic area for AbbVie, with a portfolio consisting of three marketed products - Imbruvica®, Venclexta™, and Empliciti™ and a pipeline containing multiple promising new molecules that are being studied in nearly 200 clinical trials in 19 different types of cancer. In AbbVie Oncology Early Development (OED), we strive to develop a rich and innovative pipeline of transformative cancer therapies by uniquely combining our deep knowledge in core areas of biology with cutting-edge technologies, and working together with our partners - scientists, clinical experts, industry peers, and patients - to discover and develop medicines that drive transformational improvements in cancer treatment. We are seeking a Bioassay Development Scientist to join our Analytical Development team to support the development and evaluation of newly discovered drugs and existing clinical candidates. In this lab-based role, your major responsibilities will include bioassay development, analytical testing, and molecular characterization to support the development of therapeutic antibodies, antibody variants, and antibody drug conjugates (ADC). Bachelor's Degree in biology, cell/molecular biology, or a related field with typically 5 years of applicable industry experience, or Master's Degree in biology, cell/molecular biology, or a related field with typically 2 years of applicable industry experience. Experience performing biological activity and target binding assays in a Bioassay Development group or QC lab setting within a Chemistry Manufacturing and Controls (CMC) organization. Strong working knowledge and hands-on experience with mammalian cell culture and cell-based functional assays. Demonstrated proficiency with current cell-based assay technologies and methodologies, such as cytotoxicity assays, reporter assays, and flow cytometry. Experience with ELISA, TR-FRET, AlphaScreen/AlphaLISA, Octet, and/or other binding assay platforms is desirable. Proven ability to work in a highly collaborative scientific environment. Strong verbal and written communication skills. The ideal candidate will be hard-working, self-motivated, detail-oriented, highly organized, and able to learn and adapt quickly.

Bristol-Myers Squibb is a global Biopharma company committed to a single mission: to discover, develop, and deliver innovative medicines focused on helping millions of patients around the world in disease areas such as oncology, cardiovascular, immunoscience and fibrosis. Join us and make a difference. We hire the best people and provide them with a work environment that places a premium on diversity, integrity, collaboration and personal development. Through a culture of inclusion, we create a better, more productive work environment. We believe that the diverse experiences and perspectives of all our employees help to drive innovation and transformative business results. Summary The qualified candidate is a highly motivated, interactive, and creative individual that possesses the ability to work across a highly matrixed environment to support and advance preclinical drug discovery programs. The candidate will be expected to effectively collaborate with colleagues in the oncology, immunology, protein engineering/antibody development and medicinal chemistry groups. The successful candidate will demonstrate a knowledge of mechanisms of tumor resistance to immunotherapy and a clear understanding of principals of target identification and validation, professional verbal and written communication, capable of presenting scientific results to multidisciplinary teams and key stakeholders. The primary responsibilities for this role include target validation, evaluation and modeling of cancer cell associated mechanisms of immune suppression and testing the effectiveness of therapeutic molecules using in vitro and in vivo immunological assays Qualifications A B.S. with a minimum of 7 years of experience, or an M.S. with a minimum of 4 years of academic/industrial experience with a strong scientific background and research experience in immune-oncology or oncology is required. Hands on experience with a wide range of in-vitro cellular, biochemical and immune assays (ELISA, MSD, Western blot), including isolation, culture and differentiation of human/mouse immune cell populations, MLR, T-cell proliferation assays, cytotoxicity assays Experience with multicolor flow cytometry (10-14 colors), including characterization of intra-tumor immune cell populations in mouse syngeneic tumors is required Good knowledge of cell engineering technologies, siRNA/shRNA knockdown, CRISPR-mediated genome editing, lentivirus generation and transduction of cancer cells and primary immune cells is required. Knowledge of small molecule pre-clinical drug development including knowledge of designing assays and flowcharts to identify and optimize drug candidates is preferred. Demonstrated leadership skill, independence in the experiment design, execution, data interpretation, troubleshooting and analysis of a scientific literature are required. Experience with isolation, culture and differentiation of human/mouse immune cell populations, MLR, T-cell proliferation assays, cytotoxicity assays, multicolor flow cytometry including characterization of intra-tumor immune cell populations in mouse syngeneic tumors would be valued. Ability to mentor more junior scientists and colleagues on best practices in the laboratory would be highly valued. Attention to detail with excellent organizational and record keeping skills is a requirement. Excellent interpersonal skills with the ability to interact effectively with people, internally and externally is required. Proficiency in utilizing software such as Graph Pad, Microsoft office etc. for data analysis and figure generation is required. This position is located in Redwood City, CA. There will be less than 10% travel. Bristol-Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees the resources to pursue their goals, both at work and in their personal lives.

Bristol-Myers Squibb is a global Biopharma company committed to a single mission: to discover, develop, and deliver innovative medicines focused on helping millions of patients around the world in disease areas such as oncology, cardiovascular, immunoscience and fibrosis. Join us and make a difference. We hire the best people and provide them with a work environment that places a premium on diversity, integrity, collaboration and personal development. Through a culture of inclusion, we create a better, more productive work environment. We believe that the diverse experiences and perspectives of all our employees help to drive innovation and transformative business results. The Associate Research Scientist will join the Cancer Biology Discovery Research team at Bristol-Myers Squibb in Redwood City, CA. The candidate will be expected to effectively collaborate with scientists in the Tumor Microenvironment Modulation (TME) Thematic Research Center (TRC) to develop novel therapies at the intersection of tumor, immune, and stromal biology. The qualified candidate is a highly motivated, interactive, and creative individual that possesses the ability to work across a highly matrixed environment to advance preclinical drug development programs from target identification/validation through IND enabling activities. The successful candidate will demonstrate clear and professional verbal and written communication, capable of presenting scientific results to multidisciplinary teams and key stakeholders. Qualifications: B.S. with a minimum of 5 years of experience, or an M.S. with a minimum of 3 years of academic/industrial experience with strong scientific knowledge and research experience in cancer biology/cellular and molecular biology is required. Attention to detail with excellent organizational, record keeping and interpersonal skills is required. Experience in immune-oncology and/or stromal biology research is a plus. Demonstrated independence in experimental design, execution, data analysis and troubleshooting is required. Hands on experience with a wide range of in-vitro cellular and biochemical assays, including cell culture, western blotting, immunofluorescence, immunoprecipitation, ELISAs (MSD), reporter assays, siRNA/shRNA knockdown, CRISPR-mediated genome editing, qPCR, cloning, lentivirus generation and transduction is required. Proficiency in utilizing software such as Graph Pad and Microsoft office for data analysis and figure generation is required. Working knowledge of multi-color FACS is highly desirable. This position is located in Redwood City, CA. There will be less than 10% travel. Bristol-Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees the resources to pursue their goals, both at work and in their personal lives.

Bristol-Myers Squibb is a global Biopharma company committed to a single mission: to discover, develop, and deliver innovative medicines focused on helping millions of patients around the world in disease areas such as oncology, cardiovascular, immunoscience and fibrosis. Join us and make a difference. We hire the best people and provide them with a work environment that places a premium on diversity, integrity, collaboration and personal development. Through a culture of inclusion, we create a better, more productive work environment. We believe that the diverse experiences and perspectives of all our employees help to drive innovation and transformative business results. We are looking for an Associate Research Scientist to join our In Vivo Pharmacology group to execute preclinical studies to provide in vivo data on drug candidates. This individual contributor role will collaborate across groups to plan, execute and analyze in vivo studies. Within a dynamic and engaging environment, you will interact with scientific investigators to plan and execute preclinical mouse studies. Strong technical skills and excellent communication ability are required. We value both what you do and how you do it. Requirements: Bachelor's degree with 4+ years experience working with mouse models required Experience with preclinical mouse models - oncology, immuno-oncology or immunology models using biologics and small molecules. Blood collection techniques Dosing techniques Tissue collection Basic knowledge of flow cytometry and analysis desired, but not required Data Analysis using Excel, StudyLog, Spotfire, Prizm, and similar software Bristol-Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees the resources to pursue their goals, both at work and in their personal lives.

We are seeking a capable and enthusiastic associate scientist/scientist to join our Immuno-Oncology team in Redwood City, CA. This position supports multiple projects by contributing in vitro assay development and implementation, and cell line generation. Key Responsibilities: Perform routine tasks competently and independently and generate reliable and consistent results. Analyze and critique results, noting significant deviations. Troubleshoot experiments and instrumentation. Learn and understand new experimental techniques. Demonstrate skill in multiple techniques and appropriately modify protocols, as required, to suit the changing needs of research or development sciences. Place data in proper scientific context by consulting and citing relevant literature. Demonstrate technical proficiency in his/her field. Impact projects predominantly through lab and/or pilot plant based activities. Understand and adhere to corporate standards regarding code of conduct, safety, appropriate handling of materials, controlled drug and radioactive compounds, GxP compliance, and animal care where applicable. Scientist I: Bachelor's Degree or equivalent education and typically 5 years of experience, Master's Degree or equivalent education and typically 2 years of experience. Scientist II: Bachelor's Degree or equivalent education and typically 7 years of experience, Master's Degree or equivalent education and typically 5 years of experience. For both positions: Good cell culture skills in support of primary cell assay development as well as creating and carrying cell lines for various uses. A background in immunology or cancer biology is helpful. Experience performing basic in vitro assays such as ELISAs, MSD, Luminex, ELIspot, and fluorescence-based reporter assay is desirable. Able to independently generate precise, reliable and reproducible data in a timely manner. Demonstrate experimental precision and strong data interpretation skills and should possess understanding of core discipline.

Position Description: We are seeking a senior scientist to join a talented team developing purification/downstream processes for biologics GMP applications. In this position the candidate will perform purification development, scale-up, viral clearance and technology transfer activities in a well-supported and dynamic environment to help advance novel cancer therapies to human clinical studies. Responsibilities include: Innovate, develop, optimize, and scale-up purification processes Conceive and evaluate novel advanced separation technologies and techniques Proactively seek out new information in the literature and incorporate this into individual project(s) as well as the overall program Transfer processes to GMP manufacturing for clinical material production Work with contract labs and carry out viral clearance studies Write technical publications, reports, presentations, and regulatory filings including publishing research in peer-reviewed journals and presenting work at scientific conferences Work efficiently, collaboratively, and cross-functionally toward project timelines and goals Participate on cross-functional project teams Mentor, supervise and train junior scientists; may be accountable for the effective performance of the team/individual s Basic: Doctorate (Ph.D.) degree in chemical engineering, bioengineering, or a related field, with at least 4 years of experience Must have expertise in protein purification including chromatography separations and filtration operations Able to independently design, execute, and interpret laboratory experiments to answer scientific questions Must be forward-thinking and be able to lead and contribute to scientific/technical discussions Able to independently learn, understand and execute novel/advanced scientific techniques Has excellent attention to detail and ability to keep detailed written records in lab notebook Able to author publications, technical reports, regulatory documents, and presentations Has strong communication skills including verbal, written, and scientific data presentation Has good understanding of biochemistry and bioprocess engineering concepts Able to work collaboratively within and outside of the group Has proficiency with Microsoft Office software, ability to learn new software applications Preferred: • Hands on experience with protein purification Has a strong understanding of analytical techniques, such as HPLC and ELISA Has hands on experience with monoclonal antibody or antibody-like molecule purification at GMP, pilot and/or laboratory scale Experience with AKTA chromatographic instruments (such as AKTA Avant, AKTA Purifier, AKTA Pure, AKTA Ready or similar) Demonstrated scientific aptitude through authorship of peer-reviewed publications Has a strong understanding of statistical analysis

Conceive and execute novel scientific research or development that achieves projects and area goals. Generate new scientific proposals and lead those efforts. Investigate, identify, develop, and optimize new methods and techniques. Act as a lead scientist in his/her area of expertise and critically evaluate relevant scientific and regulatory advances and integrate this knowledge into research or development programs. Key Responsibilities: Responsible for IO target identification and biological molecule development Leading and executing scientific research of early stage immune oncology discovery programs Ability to resolve key project hurdles with available information from literature and internal experts Ability to generate scientific proposal and maintain a high level of productivity in the lab Excellent skills in scientific writing for internal reports, external presentations and publications in peer-reviewed journals. May mentor/supervise small group of scientists and evaluate the performance of those individuals if management skills demonstrated Bachelor's Degree or equivalent education and typically 12 years of experience, Master's Degree or equivalent education and typically 10 years of experience, PhD and typically 4 years of experience in the area of immunology or tumor biology. Strong capability of doing multicolor flowcytometry analysis, proficiency in performing data clustering with different software and familiar with single cell related technology. Excellent skills in conventional immune assays and capability of developing comprehensive culture models containing immune cells and tumor cells. Experiences in using in vivo model to test IO therapeutics, such as syngeneic model, xenograft/PDX model, and NSG mouse model with human cell implanted. Drug development experiences in fusion protein, monoclonal antibodies, bi-specific molecules and antibody drug conjugate will be a plus. Effective writer and communicator of research or other regulatory materials.

Bristol-Myers Squibb is a global Biopharma company committed to a single mission: to discover, develop, and deliver innovative medicines focused on helping millions of patients around the world in disease areas such as oncology, cardiovascular, immunoscience and fibrosis. Join us and make a difference. We hire the best people and provide them with a work environment that places a premium on diversity, integrity, collaboration and personal development. Through a culture of inclusion, we create a better, more productive work environment. We believe that the diverse experiences and perspectives of all our employees help to drive innovation and transformative business results. A B.S. with 5 years of experience, or an M.S. with 3 years of working experience with strong scientific knowledge and research experience in cancer biology, cellular and molecular biology or immunology is required. Experience in preclinical drug discovery including knowledge and hands on experience of assay validation for optimizing drug candidates is required. Hands-on experience with a wide range of in vitro cellular and biochemical assays, preferably with cell culture, Western blotting, ELISAs (MSD), reporter assays, qPCR, HTRF, AlphaLisa and flow cytometry Proficient with Microsoft Office Suites required Prior experience with liquid handling instrumentation, automation and sample management is a plus. Experience working in diverse, multi-disciplined groups and demonstrated ability to work in a matrix work environments, manage multiple priorities, and at times, be self-directed Excellent oral and written communication skills This position is located in Redwood City, CA. Bristol-Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees the resources to pursue their goals, both at work and in their personal lives.

AbbVieData Science is the best-in-class team within its cross-industry peer group and is responsible for bringing people, process, and technology together to generate business value from clinical trials data. Our operational model is exemplified through execution and innovation. This role is key to ensuring successful delivery against the program- and study-level accountabilities assigned to Data and Statistical Sciences. Responsibilities: • Aligns DSS study teams with program- and study-level strategies. Assigned programs may include programs that are of low complexity and size. For assigned programs and studies, leads the DSS Study Team and represents DS as a member of the cross-functional study team • For assigned programs and studies, acts as single point of contact and accountable operational lead from DSS. Coordinates associated DSS study teams to meet operational objectives. Engages and connects global functional and cross-functional teams at the study level • Interacts with and influences cross-functional team members to achieve program objectives • Utilizes operational analytics and project management tools to optimize execution of programs and studies, to manage internal and external resources, to track study progress, and to prepare study status reports. Anticipates and identifies issues that could affect timelines or quality and develops options and solutions • Ensures adherence to federal regulations and applicable local regulations, Good Clinical Practices (GCPs), ICH Guidelines, AbbVie Standard Operating Procedures (SOPs), and to functional quality standards. Stays abreast of new and/or evolving local regulations, guidelines and policies related to clinical development. If assigned, participates as the DS study owner in regulatory inspections and internal quality audits • Participates in oversight of vendors and provides feedback related to clinical trial operations, issues, and trends in performance • Responsible for coaching and mentoring team members • Leads DSS innovation and process improvement initiatives and participates in cross-functional initiatives • Conducts study execution "lessons learned" across functions • May include indirect supervision of employee as well as supervision of work of contract resources • Bachelor's degree in business, management information systems, computer science, life sciences or equivalent. Master's preferred. PMP Certification or Lean Six Sigma Green Belt desired. • Must have 6+ years of pharma / clinical research / data management / health care experience or 8+ years of project management experience (and / or applicable work experience). • In-depth understanding of clinical trial processes and clinical technology. Management of a clinical trial from initiation through to completion in a lead role is preferred • Demonstrated performance as a functional leader • Demonstrated ability to influence others without direct authority • Demonstrated ability to successfully coach / mentor in a matrix environment • Demonstrated effective communication skills • Demonstrated effective analytical skills

Bristol-Myers Squibb is a global Biopharma company committed to a single mission: to discover, develop, and deliver innovative medicines focused on helping millions of patients around the world in disease areas such as oncology, cardiovascular, immunoscience and fibrosis. Join us and make a difference. We hire the best people and provide them with a work environment that places a premium on diversity, integrity, collaboration and personal development. Through a culture of inclusion, we create a better, more productive work environment. We believe that the diverse experiences and perspectives of all our employees help to drive innovation and transformative business results. The Immuno-oncology Discovery of Bristol Myers Squibb in Redwood City, CA, is seeking a highly motivated research scientist to join a group of researchers for identification of novel therapeutics in cancer immunotherapy. Building on our current successes in clinic, Yervoy (Ipilimumab) and Opdivo (Nivolumab) discovered by scientists in Bristol-Myers Squibb, we have created a dedicated effort to understand how a patient's immune response can be activated to achieve durable benefit and potentially cure, extending our understanding of cancer immunology to pursue new and innovative targets. We are seeking an outstanding individual to lead research efforts in areas of immunology that are key to understanding cancer immunity. Consideration will be given to candidates with demonstrated expertise in any of these areas: cytokine biology, T cell biology, myeloid biology, and immune cell signaling pathways Requirements: PhD, MD, DVM, or MD/DVM-PhD with at least 3 years of relevant post-doctoral research experience in immunology We are also inviting talented non-doctoral applicants who have demonstrated experience in leading therapeutic discovery Demonstrated accomplishments, as evidenced by first or senior authored publications in top-tier journals, and/or primary inventorship in patents Excellent written and oral communication skills are essential Bristol-Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees the resources to pursue their goals, both at work and in their personal lives.

Machine Learning Scientist Are you passionate about medicine and the advancement of science? Want to work on meaningful products that will revolutionize scientific discovery and medical diagnostics for years to come? We are a RAPIDLY GROWING company with late-stage venture FUNDING, on a mission to disrupt the medical & scientific community. Our proprietary technology makes DNA sequencing significantly more accessible by providing an affordable, scalable and incredibly accurate product. We are looking for a Machine Learning Scientist to join our team as we approach bringing our product to market! If you want to make a positive impact, love solving complex challenges & thrive in a fast paced environment, please apply! What You Will Be Doing -working with cross-functional team members to produce quality DNA sequencing data What You Need for this Position -MS or PhD in Computer Science, Physics or a related field -2+ years' professional experience applying machine learning in a production environment -Strong Python programming skills -Strong Tensorflow experience -Experience with time series data analysis -Strong experience developing Deep Learning models & Neural Networks and troubleshooting -Experience working with biological data is a plus What's In It for You -Competitive compensation -Stock options -Medical, dental, vision + FSA -Fully covered life insurance -401(k) -Free daily lunches and snacks! -Free onsite gym membership! -An amazing environment to learn & make an impact So, if you are a Machine Learning Scientist with experience, please apply today! - Applicants must be authorized to work in the U.S. CyberCoders, Inc is proud to be an Equal Opportunity Employer All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability, protected veteran status, or any other characteristic protected by law. Your Right to Work In compliance with federal law, all persons hired will be required to verify identity and eligibility to work in the United States and to complete the required employment eligibility verification document form upon hire.