- Takeda Pharmaceuticals (Boston, MA)
- …of my knowledge. **Job Description** **Objective & Purpose:** + Ensures adequate training support to all functional areas within Patient Safety & ... Pharmacovigilance (PSPV) in a Pharmacovigilance (PV) regulated...+ Supports the development and delivery of PSPV employee training to ensure they possess the appropriate curriculum necessary… more
- Taiho Oncology (Princeton, NJ)
- Associate Director , PV Sciences Princeton, NJ, USA Req #444 Thursday, February 27, 2025 Looking for a chance to make a meaningful difference in the oncology ... on a transformative journey with Taiho Oncology as an Associate Director in PV Sciences. At the...regulatory inspections in collaboration with team members. + Maintain training and oversight to clinical operations/ pharmacovigilance vendors… more
- Ascendis Pharma (Palo Alto, CA)
- …offer a dynamic workplace for employees to grow and develop their skills. The Associate Director , Global Pharmacovigilance Operations reports directly to the ... + Raises or increase awareness, knowledge and understanding of pharmacovigilance requirements by conducting education/ training sessions with functional… more
- Bristol Myers Squibb (Princeton, NJ)
- …in their personal lives. Read more: careers.bms.com/working-with-us . **Position Summary** The Associate Director , Therapeutic Area Audit Strategy Lead will be ... of vendors and manage external Quality Systems + Execute GCP and Pharmacovigilance audits and support GCP and Pharmacovigilance Regulatory inspections +… more
- IQVIA (Parsippany, NJ)
- …team to define, build, launch, enhance and grow the SaaS generation of Pharmacovigilance and work closely with our engineering teams and clients to guide products ... champion the products and be part the team shaping the next generation of Pharmacovigilance that impacts the lives of millions of patients across the world. **Key… more
- BD (Becton, Dickinson and Company) (El Paso, TX)
- … pharmacovigilance , post market surveillance, GMP Auditing and Supplier Management. The Associate Director , Quality Management and QA Site Leader ensures that ... and provides leadership during regulatory authority visits. The Assoc. Director leads quality programs, continuous improvement efforts, and provides quality… more
- Novo Nordisk (Plainsboro, NJ)
- …and device safety reporting regulations and ICH guidelines and internal procedures. The Associate Director Medical Review will contribute and maintain the safety ... of the company's product together with HQ. Relationships Reports to the Director of Case Review and Compliance Reporting, with cross-functional working relationships… 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 ... and/or transferable skills related to Good Clinical Practice (GCP), and/or Good Pharmacovigilance Practice (GVP). * Experience in training , supervising, line… more
- Daiichi Sankyo Inc. (Basking Ridge, NJ)
- …3rd party development. This position partners with GRLs and Clinical Safety Pharmacovigilance (CSPV) leads in the maintenance of Company Core Data Sheets (CCDS) ... we also believe in the power of collaboration. We provide employees with the training , tools and technology that they need to excel. Our open communication, emphasis… more
- Boehringer Ingelheim (Ridgefield, CT)
- …equivalent. **_Candidate will be hired_** **_at level commensurate with experience and education._** ** Associate Director Requirements:** + US MD or DO degree or ... the global Inflammation Therapeutic Area of Patient Safety and Pharmacovigilance at BI, whose priority is the wellbeing of...more than 2 years of applicable experience, required. **Sr. Associate Director Requirements:** + US MD or… more