- Takeda Pharmaceuticals (Boston, MA)
- …**Job Description** **OBJECTIVES:** + Provides oversight from a clinical research and pharmacovigilance perspective of regulated post-authorization activities ... units and the affiliate and enables them to deliver their clinical research and pharmacovigilance-related regulated activities with high compliance and agility.… more
- Ascendis Pharma (Palo Alto, CA)
- …We offer a dynamic workplace for employees to grow and develop their skills. The Associate Director , PV Vendor Management Team reports to the Director ... Safety (GPS) organization. Under the direction of the Head, PV Vendor Management Team is responsible for all Vendor...Master File (PSMF) + Work collaboratively with ICSR Management, Clinical Trial, QPPV office and Medical Safety Science team… more
- Takeda Pharmaceuticals (Boston, MA)
- …company that will inspire you and empower you to shine? Join us as a PV Risk Management Scientist/ Associate Director . At Takeda, we are transforming the ... strive for excellence in everything we do. As an Associate Director / PV Risk Management...(eg patient preference studies) + Collaborate with Safety Leads, Clinical Leads, PV scientists and Clinical… more
- Takeda Pharmaceuticals (Boston, MA)
- …**Job Description** **About the role:** As a member of Takeda Oncology, as an Associate Director , your work will contribute to our bold, inspiring vision: We ... strategic training program for the Oncology pipeline, including Polycythemia Vera ( PV ) disease state education. + Provide coaching for Regional Directors, Oncology… more
- Actalent (Frederick, MD)
- …ideal candidate will be a highly motivated professional who can oversee Quality Assurance clinical operations. The Associate Director of QA will oversee ... Description Quality Assurance Director with extensive experience in biopharmaceutical quality assurance...Pharmacovigilance ( PV ) Quality Management System (QMS) and PV System for clinical and commercial operations,… more
- Sumitomo Pharma (Augusta, ME)
- …seeking a dynamic, highly motivated, and experienced individual for the position of ** Associate Medical Director .** The Associate Medical Director ... products. + Conduct safety surveillance over product life cycle, reviewing clinical trial and post-marketing Individual Case Safety Reports (ICSRs), including… more
- Takeda Pharmaceuticals (Boston, MA)
- …improvement + Lead CPMQ continuous improvement initiatives to enable optimization of clinical and safety quality compliance activities. + Provide expert advice and ... metrics for CPMQ activities eg audit, inspection, QE, CAPA. + Organise Clinical and Pharmacovigilance Quality council meetings and proactively manage the agenda and… more
- AbbVie (Irvine, CA)
- …and Tik Tok (https://www.tiktok.com/@abbvie) . Job Description Purpose: Group Medical Director manages other Associate Medical Directors, Medical Directors, ... development, and discovery + Works closely with Executive Medical Director to establish safety strategy for each indication and...industry, and regulatory authorities + A clear understanding of PV and clinical development and monitoring … more
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