- Daiichi Sankyo, Inc. (Bernards, NJ)
- …pharmaceutical therapies to improve standards of care and address diversified, unmet medical needs of people globally by leveraging our world-class science and ... around rare diseases and immune disorders. Summary: Oversees Local/Global Pharmacovigilance (PV) service providers responsible for Call Center, individual safety… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …lives for a living. Are you ready to make a difference? The Position The Director Medical Review oversees a team of Medical Reviewers responsible for ... Case Safety Reports and other safety reports pertaining to Novo Nordisk Products. The Medical Review Director is a key Leadership Team member and advisor on… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- About the Department The Clinical, Medical and Regulatory (CMR) department at Novo Nordisk is one of the most diverse and collaborative groups within the ... and developing and implementing regulatory strategies with the FDA to providing medical education and collecting data to support efficacy and new product… more
- Lupin Pharmaceuticals (Coral Springs, FL)
- OverviewThe Respiratory Clinical Development Medical Lead will oversee the clinical and medical aspects of new respiratory medicines, including new drug or ... This role involves strategic leadership in clinical trials, clinical sciences, medical monitoring, target product profile (TPP) development, due diligence projects,… more
- Merck & Co. (Montgomery County, PA)
- …interactions and case management.Act as primary liaison with commercial, medical affairs, market access, legal/compliance, pharmacovigilance , and external ... the Pipeline Advertisemen We are currently recruiting for several Associate Director positions within US Marketing, covering Physician (HCP), Consumer (HCC),… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- About the Department The Clinical, Medical and Regulatory (CMR) department at Novo Nordisk is one of the most diverse and collaborative groups within the ... and developing and implementing regulatory strategies with the FDA to providing medical education and collecting data to support efficacy and new product… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …pharmaceutical therapies to improve standards of care and address diversified, unmet medical needs of people globally by leveraging our world-class science and ... areas centered around rare diseases and immune disorders. Job Summary: The Director of Data Management (DM) Reporting provides leadership in Data Management… more
- Merck & Co. (Rahway, NJ)
- …Training Programs, FDA Regulations, IT Coordination, IT Operation, Pharmacovigilance , Policy Implementation, Regulatory Compliance, Regulatory Labeling, Regulatory ... applicable.We offer a comprehensive package of benefits.- Available benefits include medical , dental, vision healthcare and other insurance benefits (for employee… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …pharmaceutical therapies to improve standards of care and address diversified, unmet medical needs of people globally by leveraging our world-class science and ... global role that will cover signal activity across all DS regions. The Associate Director of the Signal Management Center of Excellence (CoE) will lead the daily… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- … case processing experience is preferred Experience in patient safety or pharmacovigilance preferred Knowledge of medical terminology required Knowledge of ... About the Department The Clinical, Medical and Regulatory (CMR) department at Novo Nordisk...projects in Patient Safety. Relationship Reports directly to the Director , Patient Safety Case Management. This role involves the… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- About the Department The Clinical, Medical and Regulatory (CMR) department at Novo Nordisk is one of the most diverse and collaborative groups within the ... and developing and implementing regulatory strategies with the FDA to providing medical education and collecting data to support efficacy and new product… more
- Merck & Co. (North Wales, PA)
- Job DescriptionOur Clinical and Pharmacovigilance teams manage studies to provide the safety and efficacy data required for regulatory approval of potential new ... technology and applying rigorous scientific and ethical standards.The Senior Director (Senior Principal Scientist) has primary responsibility for the planning… more
- Merck & Co. (North Wales, PA)
- …and pipeline products to produce safe, effective, innovative medicine.The Clinical Director is responsible for protocol development and medical / scientific ... Job DescriptionOur Clinical Research and Pharmacovigilance team pushes the boundaries of global healthcare...including but not limited to the design, oversight and medical monitoring of Phase I to V clinical trials,… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- About the Department The Clinical, Medical and Regulatory (CMR) department at Novo Nordisk is one of the most diverse and collaborative groups within the ... and developing and implementing regulatory strategies with the FDA to providing medical education and collecting data to support efficacy and new product… more
- Kelly Services (South San Francisco, CA)
- **Kelly(R) Science & Clinical** is seeking a Medical Director of Pharmacovigilance for a fulltime, Direct Hire role with a pharmaceutical client based in the ... within the continental US The position will report to Senior Director , Medical Monitoring and Pharmacovigilance . **Key Duties& Responsibilities:** Key… more
- AbbVie (Chicago, IL)
- …and CAPA investigations as necessary Qualifications + MD or equivalent + Associate Medical Director I - Drug safety experience preferred but not required ... that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a...Purpose: The primary focus of this position is the medical review of clinical trial SAEs including causality assessment… more
- Takeda Pharmaceuticals (Boston, MA)
- …my knowledge. **Job Description** **About the role:** Join Takeda as a Senior Medical Director , Pharmacovigilance in Gastrointestinal and Inflammation (GI2). ... and Governance. As part of the Patient Safety and Pharmacovigilance (PSPV) team, you will report to the Vice...the Takeda Safety Board and similar forums. The Senior Medical Director will be a key player… more
- Amgen (Washington, DC)
- …us and transform the lives of patients while transforming your career. Director of Observational Research, Pharmacovigilance Epidemiology and Causal Inference ... world. In this vital role you will lead a Pharmacovigilance Epidemiology and Causal Inference team within the Data...within the Data and Analytics Center (DAC). A CfOR director is recognized as a strong scientific contributor and… more
- Gilead Sciences, Inc. (Foster City, CA)
- …Join Gilead and help create possible, together. **Job Description** The Associate Director , Good Pharmacovigilance Practice (GVP) Audits, serves as a key ... lead complex audits across the broader R&D, vendor, and pharmacovigilance workstreams. This position requires close collaboration with cross-functional stakeholders,… more
- Takeda Pharmaceuticals (Boston, MA)
- …**OBJECTIVES:** + Provides oversight from a clinical research and pharmacovigilance perspective of regulated post-authorization activities in the commercial business ... affiliate and enables them to deliver their clinical research and pharmacovigilance -related regulated activities with high compliance and agility. + Establish and… more
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