- Otsuka America Pharmaceutical Inc. (Boise, ID)
- **Job Summary** Otsuka is looking for a strong Clinical Statistician in the Medical and Real World Data Analytics organization to provide statistical expertise for ... analysis of clinical trials data beyond the study endpoints, including secondary,...scientists and data programmers, and external stakeholders including Medical Affairs , Value and Real World Evidence to provide end-to-end… more
- Otsuka America Pharmaceutical Inc. (Jackson, MS)
- **Position Summary:** The Director GVE Operations oversee and coordinates projects within the department to ensure alignment with organizational goals. This role is ... other integrated data generation initiatives. This position reports to the Senior Director , Global Integrated Evidence & Innovation Operations and can be based in… more
- Bristol Myers Squibb (Princeton, NJ)
- …optimize brand strategy and execution. + Work closely with sales, market access, regulatory , and medical affairs teams to align marketing initiatives with ... and in their personal lives. Read more: careers.bms.com/working-with-us . **Associate Director - US GI Marketing - Hepatocellular Carcinoma (HCC)** **Position… more
- Bristol Myers Squibb (Madison, NJ)
- …their personal lives. Read more: careers.bms.com/working-with-us . **Summary:** The Associate Director of US Access Marketing is responsible for developing and ... for Breyanzi. This individual will report to the Executive Director of US access strategy and will work closely...other matrix partners such as commercial, Legal, Medical and Regulatory functions and cross functional partners such as US… more
- Otsuka America Pharmaceutical Inc. (Oklahoma City, OK)
- …& Translational Medical, Clinical Development, Value and Real-World Evidence, Regulatory , Medical Affairs , Data and Analytics, Digital Health and Commercial ... evidence generation strategy, operational excellence and digital innovation. The Director , Global Integrated Evidence Strategy is an important leadership position… more
- Merck (Boston, MA)
- …information clearly and concisely to diverse audiences, including researchers, clinicians, regulatory affairs professionals, and other stakeholders + Familiarity ... through information science. We are seeking a passionate, experienced Associate Director to connect scientists and stakeholders with focused scientific literature… more
- Banner Health (Tucson, AZ)
- …responsibility for the Department's financial and operational performance in its clinical practice, research, and educational and training activities. This position ... department in the College of Medicine (UACOM), and its clinical business enterprise which operates, in a variety of...Officer and the Deputy Dean for Financial and Administrative Affairs of the UACOM to develop and monitor operating… more
- Merck (Rahway, NJ)
- …with a cross-functional group of experts in commercialization, regulatory affairs , statistics, and manufacturing to manage clinical development projects + ... monitoring, analysis, regulatory reporting, and publication. **Specifically, the Senior Director may be responsible for:** + Evaluating pre- clinical and… more
- Merck (Upper Gwynedd, PA)
- …with a cross-functional group of experts in commercialization, regulatory affairs , statistics, and manufacturing to manage clinical development projects; and ... clinical development, including study design, placement, monitoring, analysis, regulatory reporting, and publication. Specifically, the Senior Director may… more
- Gilead Sciences, Inc. (Foster City, CA)
- …& Manufacturing (PDM) and partner with Quality, Supply Chain, Manufacturing, CMC Regulatory Affairs , Clinical Development and Technical Development to ... **Job Description:** **We are seeking a talented and highly motivated Director for our Structural Characterization team in Biologics Pivotal and Commercial… more