- University of Miami (Miami, FL)
- …of Executive Dean of Research is currently seeking a Clinical Research Safety Associate to work in Miami. The Clinical Research Safety Associate (CRSA) ... The CRSA works closely with clinical research, regulatory affairs, and pharmacovigilance teams to maintain the safety and compliance of investigational products.… more
- Takeda Pharmaceuticals (Cambridge, MA)
- …will inspire you and empower you to shine? Join us as an Associate Medical Director, Clinical Science in our Gastrointestinal & Inflammation Therapeutic Area Unit ... vital contributor to our inspiring, bold mission **POSITION OBJECTIVES:** The Associate Medical Director leads and drives strategy for the overall global… more
- Takeda Pharmaceuticals (Boston, MA)
- …to inspire you and empower you to shine? Join us as the Associate Director, Supplier Relationship Management (Central/Specialty Labs) based remotely reporting to the ... project management, clinical monitoring, data management process, regulatory affairs, pharmacovigilance , etc.) to enable meaningful dialogue within Takeda and with… more
- Bristol Myers Squibb (Phoenix, AZ)
- …data generation, insight generation and patients' access to medicine. The Regional Associate Director (RAD) role is field-based and focused on managing a team ... Adverse Events (AEs) and fully understand and comply with BMS Pharmacovigilance SOPs regarding identification and reporting timelines + Contributes to managing… more
- Haleon (Warren, NJ)
- …In line with a risk-proportionate framework for product vigilance, the ** Associate Director, Consumer Safety Science** is accountable for developing the safety ... + 5 years+ experience in similar role with extensive knowledge in pharmacovigilance . + In-depth knowledge in causality assessment, evaluation of safety signals and… more
- Insight Global (Wilmington, DE)
- Job Description We are seeking an Associate Director to oversee our pharmaceutical client's Robotic Process Automation (RPA) and AI/ML portfolio, collaborating with ... and drug development areas (Clinical Operations, Data Management, Regulatory Affairs, Pharmacovigilance , Finance, HR, Medical Affairs) null We are a company… more
- AbbVie (North Chicago, IL)
- …be added to our talent pipeline and considered for future opportunities. The Associate Director (AD) of Epidemiology in Pharmacovigilance & Patient Safety leads ... the scientific strategy for pharmacoepidemiology and real-world evidence to support product development and safety across therapeutic areas. They will design and interpret studies, contribute to regulatory submissions, and provide expertise in regulatory… more
- Regeneron Pharmaceuticals (Armonk, NY)
- The Associate Director, Global Development Quality Inspection Management (GDQIM) acting as an Inspection Management Lead (IML) is a key position that is responsible ... transferable skills related to Good Clinical Practice (GCP), and/or Good Pharmacovigilance Practice (GVP). * Experience in training, supervising, line management,… more
- Gilead Sciences, Inc. (Parsippany, NJ)
- …research through post-marketing + Strong experience in Good Clinical and Good Pharmacovigilance Practices and knowledge of evolving regulations, such as ICH E6 R3 ... + Proven experience advising business functions in the biopharma industry on quality and compliance requirements and continuous improvement + Experience working across a broad spectrum of quality and/or compliance activities, including authoring SOPs, leading… more
- AbbVie (Mettawa, IL)
- …subject matter experts and advisors from cross-functional teams including pharmacovigilance , legal, regulatory, medical, office of ethics and compliance (OEC) ... and business technology solutions (BTS) to ensure operational excellence and governance of EPE led processes. + Monitor the external environment, to help to drive AbbVie's patient experience capability, proactively reviewing and identifying opportunities to… more