- 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 ... and functions + Collaborate with teams (eg, Safety, Regulatory, Clinical , IT) to embed PV data standards into systems and workflows across the organization… more
- Lilly (Indianapolis, IN)
- …to make life better for people around the world. **Job Responsibilities:** The Sr. Director PV Case Management ICSR provides technical leadership for the design, ... for managing key ICSR vendor relationships. In addition, the Sr. Director leads global projects involving complex safety systems, ensuring strategy and… 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
- 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 ... Ascendis Safety Database as assigned. + Functions as a PV advisor to Ascendis Clinical Development Organizations,...team (specifically from: Talent Acquisition Partner or Human Resources Director ) is not allowed. If this occurs your ownership… more
- Parexel (Columbia, SC)
- …success, we are expanding our esteemed Medical Sciences Team and seeking an Associate /Medical Director to support the growth of our Global Immunology and ... Inflammation Therapeutic Franchise. As an Associate / Medical Director , you will work...the development and/or review of study documents, such as clinical protocols, Medical Monitoring Plans (MMP), integrated clinical… 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 ... quality. **HOW YOU CONTRIBUTE** + Lead strategic quality oversight activities for clinical , laboratory, medical, and PV suppliers. + Develop, execute, and… 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...Pharmacist, or similar. + Minimum of 10 years of Clinical Trial and Post-marketing Pharmacovigilance ( PV ) experience… more
- BeOne Medicines (San Mateo, CA)
- …+ Experience working with Life Sciences data, including exposure to R&D, Clinical Operations, TechOps, or Manufacturing domains. Understanding of key systems (CTMS, ... EDC, eTMF, LIMS, MES, PV systems), data models (CDISC, SDTM, ADaM), and typical data challenges (quality, lineage, integration, governance) is highly desirable… more
- Boehringer Ingelheim (Ridgefield, CT)
- …be an asset. + People leadership potential required. Senior Associate Director : + Total applicable experience (incl. clinical practice, plus research or ... **Description** Director OR Senior Associate Director...relevant industry) of greater than three (3) years required. Director : + Total applicable experience (incl. clinical … more