- Bristol Myers Squibb (Madison, NJ)
- …of key functions (eg, early development, TM, clinical pharmacology, toxicology, regulatory , HEOR, market access, medical affairs ), applying foresight, scientific ... and will supervise and have accountability for the clinical components of regulatory filings. * Will contribute to overall Therapeutic Area disease strategy while… more
- Otsuka America Pharmaceutical Inc. (Trenton, NJ)
- …to a direct report responsible for day-to-day execution. While initially focusing on Medical Affairs , the vision is to cover all R&D HCP engagement over time. This ... Excellence & Operations Vendor and Contracts Management Lead and directly manages the Manager , HCP Engagement Lead. This position will lead the transformation of how… more
- Sanofi Group (Morristown, NJ)
- …Clinical Operations (EDCO, including Clinical Trial Managers and Data Managers), Regulatory Affairs , Patients Safety & Pharmacovigilance, Therapeutic Area ... Clinical Operations (EDCO, including Clinical Trial Managers and Data Managers), Regulatory Affairs , Patients Safety & Pharmacovigilance, Therapeutic Area… more
- Bristol Myers Squibb (Princeton, NJ)
- …policy innovation that align with organizational objectives. + Analyze legislative and regulatory developments impacting the IRA and Medicare Part D and develop BMS ... access under Part D. + Collaborate with internal teams (legal, government affairs , market access) to align advocacy efforts. + Lead cross-functional workgroups to… more
- Bristol Myers Squibb (Princeton, NJ)
- …in Immunology or Pulmonology is preferred. + Should be experienced in Medical Affairs (US and WW) , preferred Medical Strategy, ideally with experience in medical ... + Familiarity with all phases of drug development, including clinical development, regulatory and life cycle management. + Healthcare landscape knowledge & insight.… more
- J&J Family of Companies (Raritan, NJ)
- …Management, Project Integration Management, Quality Assurance (QA), Quantitative Research, Regulatory Affairs Management, Standard Operating Procedure (SOP), ... encompassing all phases of development. Provides input and oversight of regulatory submission strategy related to functional deliverables, where applicable. +… more
- Bristol Myers Squibb (Princeton, NJ)
- …Focus and Associated Responsibilities **Patients to Pipeline Global Law ( Regulatory Law, Worldwide Therapeutic Areas, Commercialization and Development)** + Develop ... an understanding of the legal and regulatory framework applicable to the commercialization and development of pharmaceutical products. + Provide solutions-oriented… more
- BD (Becton, Dickinson and Company) (Franklin Lakes, NJ)
- …Ensure program success by working cross functionally with R&D-Engineering, Marketing, Medical Affairs , Manufacturing, Quality and Regulatory Affairs . + ... Description Summary** The R&D Senior Scientist reports directly to the Senior R&D Manager and is responsible for delivering technical excellence in the area of… more
- Bristol Myers Squibb (Princeton, NJ)
- …with functional areas outside of medical including marketing, sales, access, legal, regulatory , clinical operations, and research and development + Ensure US medical ... PharmD, DNP) + Prior (3-5+ years) pharmaceutical industry experience in medical affairs is preferred + Highly organized and motivated individual with the ability… more
- Sanofi Group (Morristown, NJ)
- **Job Title:** Clinical Outcome Assessment (COA) Lead **Grade:** L3 **Hiring Manager :** Benoit Arnould **Location** : Cambridge, MA or Morristown, NJ (Hybrid policy ... new COA instruments; the development of briefing books or dossiers for regulatory consideration of COAs Internal customers include primarily Research and Development… more