- Merck & Co. (Rahway, NJ)
- …supports statistical programming activities for multiple and/or late stage drug / vaccine clinical development projects. -Accountability predominantly includes the ... that include coordinating the activities of a programming team.US and/or worldwide drug or vaccine regulatory application submission experience at the leadership… more
- Merck & Co. (Rahway, NJ)
- Job Description Position Description This position is for a principal scientist in biostatistics.-The candidate should have a solid knowledge of statistical ... analysis of clinical trials; Experience with regulatory filing for approval of drug / vaccine products; Prior experiences with immunology clinical trials design,… more
- Merck & Co. (North Wales, PA)
- …the statistical programming activities for multiple and/or large/complex late-stage drug / vaccine clinical development projects.Develop and execute statistical ... procedures, SAS/MACRO, SAS/GRAPH and systems and database expertise;US and/or worldwide drug or vaccine regulatory application submission experience at the… more
- Merck & Co. (South San Francisco, CA)
- …development and is an integral part of our Company's powerful world-class network of drug and vaccine discovery.At our Company, we are inspired by the belief ... advancing your career.Our Company is currently seeking a highly motivated and exceptional scientist in the Chemistry Modeling & Informatics group at our South San… more
- Merck (West Point, PA)
- **Job Description** Vaccine Drug Product Development, a part of our company's Research Laboratories, is seeking a Principal Scientist to join our ... department in West Point, PA. Our mission is to develop novel vaccine drug products that will profoundly improve global human health-directly building from our… more
- Merck (Rahway, NJ)
- …and routes of administration, including inhalation, implantation, and injection. The Associate Principal Scientist will lead the definition and execution of ... which focuses on the design, development, and commercialization of novel biologic/ drug / vaccine -device combination products for safe and effective delivery to… more
- Merck (West Point, PA)
- …model-based scientific and business insights across all phases of drug and vaccine development. Additionally, the scientist serves as the Health Economic and ... **Job Description** Principal Scientist /Director provides strategic development and implementation of cutting-edge mathematical and economic models to enhance… more
- Merck (Rahway, NJ)
- **Job Description** **Position Description** This position is for a principal scientist in biostatistics. The candidate should have a solid knowledge of ... analysis of clinical trials; Experience with regulatory filing for approval of drug / vaccine products; Prior experiences with immunology clinical trials design,… more
- Merck (South San Francisco, CA)
- …clinical development and is an integral part of our Company's powerful world-class network of drug and vaccine discovery. At our Company, we are inspired by the ... your career. Our Company is currently seeking a highly motivated and exceptional scientist in the Chemistry Modeling & Informatics group at our South San Francisco,… more
- Merck (Rahway, NJ)
- …supports statistical programming activities for multiple and/or late stage drug / vaccine clinical development projects. Accountability predominantly includes the ... the activities of a programming team. + US and/or worldwide drug or vaccine regulatory application submission experience at the leadership level including the… more
- Merck (North Wales, PA)
- …Lead the statistical programming activities for multiple and/or large/complex late-stage drug / vaccine clinical development projects. + Develop and execute ... and systems and database expertise; + US and/or worldwide drug or vaccine regulatory application submission experience at the leadership level including… more
- Pfizer (Pearl River, NY)
- **ROLE SUMMARY** The primary purpose is to serve as a Clinician within a Pfizer vaccine development program. This role may serve as a clinical lead for one or more ... clinician medical monitor may delegate these responsibilities to the study clinician scientist identified in the SSRP. The specific components of safety data review… more
