- Lilly (Indianapolis, IN)
- …determined to make life better for people around the world. The purpose of the Associate Director PV Systems Strategy and Implementation is to develop, ... implement, and maintain streamlined and compliant systems that enable the PV organization's objectives. This role will work with stakeholders to analyze workflows… more
- CSL Behring (King Of Prussia, PA)
- …to developing therapies that make a meaningful difference worldwide. Could you be our next Associate Director , PV Standards and Governance? The job is in our ... will establish and maintain global standards, policies, and governance frameworks for pharmacovigilance ( PV ) data and processes. You will ensure compliance,… 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
- Ascendis Pharma (Princeton, NJ)
- …We offer a dynamic workplace for employees to grow and develop their skills. The Associate Director , ICSR Management Team reports to the Director , Head, ICSR ... Business Partner agreements. + Responsible for operational activities of ICSRs processed by PV Vendor and provide feedback and guidance as applicable. Assists in the… more
- CSL Behring (King Of Prussia, PA)
- …therapies that make a meaningful difference worldwide. We are looking for a ** Associate Director ,** **Case Management Intake & Submissions** to join our R&D ... schedule_ _. #LI-hybrid_ **The Role:** Reporting to the Sr. Director , Global Case Management, you will: + Oversee intake...Minimum of 10 years of Clinical Trial and Post-marketing Pharmacovigilance ( PV ) experience with 5 years of… more
- Takeda Pharmaceuticals (Boston, MA)
- …true to the best of my knowledge. **Job Description** **ABOUT THE ROLE** The Associate Director , GCP Audit & Compliance provides strategic quality oversight to ... clinical, medical, and pharmacovigilance suppliers across Takeda's global network. You will lead...strategic quality oversight activities for clinical, laboratory, medical, and PV suppliers. + Develop, execute, and continuously improve the… more
- Boehringer Ingelheim (Ridgefield, CT)
- **Description** Director OR Senior Associate Director has responsibility for the pharmacovigilance risk management activities of marketed and/or ... subspecialty would be an asset. + People leadership potential required. Senior Associate Director : + Total applicable experience (incl. clinical practice, plus… more