- Otsuka America Pharmaceutical Inc. (Princeton, NJ)
- …but not limited to Translational Research & Biomarkers, Clinical Management, Global Regulatory Affairs , Global Clinical Development (late phase), Data & ... on the early development CNS portfolio and Early Development Teams. This Senior Director is a strategic scientific and clinical leader accountable for the… more
- AbbVie (North Chicago, IL)
- …research programs; for generating scientific evidence to support medical affairs strategies; and for interacting with regulatory agencies, medical community, ... they are scientifically sound, aligned with the product strategy, and meet scientific and/or applicable regulatory needs. Ensure statistical methodology is… more
- BeOne Medicines (Emeryville, CA)
- …**Cross-Functional & External Engagement** + Serve as the analytical liaison across GCO, Regulatory , Medical Affairs , Access, and Corporate Affairs to ensure ... **General Description:** Reporting to the Head/ Director of Clinical Trial Diversity, the Associate Director will operationalize BeOne's clinical trial diversity… more
- Sanofi Group (Morristown, NJ)
- **Job Title:** US Medical Director , Dermatology (NextGen Immunology) **Location** : Cambridge, MA Morristown, NJ **About the Job** A strategic medical leadership ... role within Sanofi's Next Gen Immunology Medical Affairs organization, driving evidence-based medical strategy in dermatology and rheumatology therapeutic areas.… more
- Astellas Pharma (Northbrook, IL)
- …with rigorous statistical insight. + Collaborate with Clinical Development, Medical Affairs , Regulatory , Market Access, and Commercial to ensure alignment ... Scientific contributions through publications, presentations, or participation in industry/ regulatory working groups. + Experience working with real-world data… more
- J&J Family of Companies (Spring House, PA)
- …Design Mindset, Drug Discovery Development, Industry Analysis, Innovation, Market Research, Regulatory Affairs Management, Research Ethics, Scientific ... partnership with the Compound Development Team (CDTL) and project management, global regulatory affairs , clinical pharmacology, health economics, and the disease… more
- Gilead Sciences, Inc. (Santa Monica, CA)
- …their aspirations. Join Kite and help create more tomorrows. **Job Description** The Director , Medical Affairs , US Real World Evidence Center of Excellence is ... clinicians + Providing leadership and oversight of non-interventional study protocols, regulatory documents, and scientific publications + Provide excellent… more
- Bristol Myers Squibb (Princeton, NJ)
- …and in their personal lives. Read more: careers.bms.com/working-with-us . The Senior Director for Milvexian Global Medical Strategy will provide deep disease state ... focus on strategy, planning, development, and implementation of the medical plan. The Director will report to the Executive Director , Thrombosis Disease Area… more
- Merck (Rahway, NJ)
- …Work closely with a cross-functional group of experts in commercialization, regulatory affairs , statistics, and manufacturing to manage clinical development ... including development strategy, study design, initiation, execution, monitoring, analysis, regulatory reporting, and publication. **Specifically, the Senior Director… more
- AbbVie (North Chicago, IL)
- …of an overall Product Development Plan, based on strong medical and scientific principles, knowledge of compliance and regulatory requirements, AbbVie's ... generate, deliver, and interpret high-quality clinical data supporting overall product scientific and business strategy. Responsibilities: + Manages the design and… more