- Boehringer Ingelheim (Ridgefield, CT)
- **Description** Director OR Senior Associate Director has responsibility for the pharmacovigilance risk management activities of marketed and/or ... the BI-internal Asset Benefit Risk Team, consisting of experts in Pharmacovigilance , Medical Affairs, Epidemiology and Biostatistics and other disciplines… more
- Otsuka America Pharmaceutical Inc. (Princeton, NJ)
- …training programs in GxP compliance, Ethics & Compliance, and Pharmacovigilance , ensuring alignment with regulatory requirements and business objectives. This ... (Good Manufacturing/Clinical/Laboratory Practice) compliance + Ethics and Compliance + Pharmacovigilance + Partner with Quality, Regulatory, R&D, Manufacturing, Supply… more
- Otsuka America Pharmaceutical Inc. (Waltham, MA)
- **Job Summary** The Senior Director will serve as the Translational Medicine CNS Therapeutic Area Head, reporting to the VP, Translational Medicine and Early ... Clinical Development within OPDC's Early Development Organization (EDO). The Senior Director Translational Medicine will oversee a small team of CNS… more
- Sanofi Group (Cambridge, MA)
- **Job Title:** Senior Clinical Research Director **Location:** Cambridge, MA or Morristown, NJ **About the Job** Join the engine of Sanofi's mission - where deep ... turn the impossible into possible for millions. As the ** Senior Clinical Research Director ** ( Senior ...improve people's lives. **Main Responsibilities:** The role of the Senior CRD is to: + Provide medical … more
- Sanofi Group (Morristown, NJ)
- **Job Title:** Senior Clinical Research Director **Location:** Morristown, NJ Cambridge, MA **About the Job** Join the engine of Sanofi's mission - where deep ... could turn the impossible into possible for millions. The Senior Clinical Research Director (CRD) is an...Senior CRD is to: + Provide ophthalmology focused medical and scientific expertise to the cross functional project… more
- Lilly (Indianapolis, IN)
- …inform Medical Review work. + Present strong understanding of pharmacovigilance and clinical research principles, regulations, and be able to interpret complex ... life better for people around the world. **Purpose:** The Case Management Medical Review Scientist is responsible for conducting comprehensive medical review… more
- Lilly (Durham, NC)
- …are determined to make life better for people around the world. **Responsibilities** The Senior Director , Global Process Owner for Quality Risk Management, as a ... agency standards, industry trends and scientific principles. **Key Objectives/Deliverables** The Senior Director , Global Process Owner for Quality Risk… more
- Teva Pharmaceuticals (West Chester, PA)
- Director , Senior Counsel, Global R&D Compliance Date: Dec 10, 2025 Location: West Chester, United States, Pennsylvania, 19380 Company: Teva Pharmaceuticals Job ... a difference, and new people to make a difference with. **The opportunity** The Director , Senior Counsel, Global R&D Compliance role reports into our Global R&D,… more
- Takeda Pharmaceuticals (Cambridge, MA)
- …of Quality/Compliance experience. + Advanced knowledge of clinical research (GCP), pharmacovigilance (GVP) and medical throughout R&D and commercialization, and ... are resourced, prioritized, and expeditiously reported. + Serves as a senior strategic Quality Partner to relevant R&D stakeholders and strategic suppliers.… more
- AbbVie (Irvine, CA)
- …medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's ... in support of the overall product development plan, based on strong medical and scientific principles, knowledge of compliance and regulatory requirements, AbbVie's… more