- Daiichi Sankyo, Inc. (Bernards, NJ)
- …areas centered around rare diseases and immune disorders. Job Summary: The Sr. Director , Clinical Safety MD, will lead the development and implementation of ... the optimum benefit-risk for Development Sankyo's development compounds through the Safety Management Team framework. This individual will use strong leadership and… more
- Merck & Co. (Boston, MA)
- Job DescriptionThe Senior Director (Sr. Principal Scientist) has primary responsibility for the planning and directing clinical research activities involving new ... all phases of clinical development (pre-clinical to post-licensure). The Senior Director will manage the entire cycle...the clinical findings from studies to support decisions regarding safety and efficacy as well as new drug applications,… more
- Tris Pharma (Monmouth Junction, NJ)
- …Director / Director , Procurement. Title and salary commensurate with experience. The Director / Senior Director , Procurement is responsible for multiple ... Administration (FDA), Drug Enforcement Administration (DEA), and Occupational Health and Safety Administration (OSHA) regulations, as well as all applicable company… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …future capabilities. We're responsible for regulating accounting, upholding workplace safety , managing our supply chain and sampling, supporting technological and ... IT teams to ensure a strong data and technology foundation Engage senior leaders to drive strategic technology transformations Physical Requirements 10-20% overnight… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …across all Medical Affairs programs. This role involves deputizing for the Sr. Director , representing the Quality organization at senior levels. The Director ... and immune disorders. Job Summary: Reporting to the Sr. Director , Medical Affairs QA, the Director of...broad understanding of post marketing studies and post approval safety studies (PASS).Demonstrated experience and proven track record of… more
- Genmab (NJ)
- …have you join us!The Global Regulatory Labeling, Policy and Intelligence Associate Director will primarily be responsible for leading the development and maintenance ... will be within Global Regulatory Affairs (GRA) and will report to the Sr. Director , Labeling, Policy and Intelligence. The position may be based in our Princeton,… more
- Formation Bio (New York, NY)
- …to bring new treatments to patients faster and more efficiently.About the PositionAs AD/ Director of Data Science - Platform at Formation Bio, you will lead one ... of sophisticated models to predict clinical outcomes-determining drug efficacy, safety profiles, and optimal indications-to create a data-driven portfolio that… more
- Merck & Co. (Rahway, NJ)
- …integrating state-of-the-art technology and applying rigorous scientific and ethical standards.The Senior Director ( Senior Principal Scientist) has primary ... Clinical and Pharmacovigilance teams manage studies to provide the safety and efficacy data required for regulatory approval of...to post-licensure). With a focus on late-stage development, the Senior Director will manage the entire cycle… more
- Merck & Co. (Rahway, NJ)
- Job Description-The Senior Director ( Senior Principal Scientist) has primary responsibility for planning and directing clinical research activities involving ... respiratory medicines. With a focus on late-stage development, the Senior Director will manage the entire cycle...summarizing clinical findings from studies to support decisions regarding safety and efficacy as well as new drug applications,… more
- Merck & Co. (Rahway, NJ)
- …with talented and dedicated colleagues while developing and expanding your career. Senior Director ( Senior Principal Scientist) has primary responsibility ... span all phases of clinical development (pre-clinical to post-licensure).The Senior Director will manage the entire cycle...the clinical findings from studies to support decisions regarding safety and efficacy as well as new drug applications,… more
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