- Takeda Pharmaceuticals (Boston, MA)
- …to the best of my knowledge. **Job Description** **About the role:** The Associate Director, Clinical and Safety Quality Compliance is responsible for ensuring the ... compliance teams for regulations impacting Clinical, Safety and Clinical Pharmacovigilance Medical Quality (CPMQ) processes and procedures and determined by… more
- Ascendis Pharma (Princeton, NJ)
- …We offer a dynamic workplace for employees to grow and develop their skills. Associate Director, Global Patient Safety Medical Science reports to Head of GPS Medical ... + Assists Head of GPS Medical Science for drug safety and pharmacovigilance activities for ensuring corporate compliance with all applicable laws and regulations… more
- Amgen (Washington, DC)
- …Join us and transform the lives of patients while transforming your career. **Senior Associate , R&D Compliance** **What you will do** Let's do this! Let's change the ... Qualifications:** + High school/GED + 4 years quality compliance work experience OR Associate 's + 2 years quality compliance work experience OR Bachelor's + 6 months… more
- Daiichi Sankyo Inc. (Basking Ridge, NJ)
- …areas centered around rare diseases and immune disorders. **Summary:** The Associate Director, Laboratory Data Management is accountable for the end-to-end delivery ... Sankyo R&D collaborating with clinical and medical teams, clinical safety and pharmacovigilance , CROs and other vendors to ensure high quality of laboratory data… more
- Daiichi Sankyo Inc. (Basking Ridge, NJ)
- …areas centered around rare diseases and immune disorders. **Summary:** The Associate Director, Data Management Processes, Training and Inspection Readiness, is ... Sankyo R&D collaborating with clinical and medical teams, clinical safety and pharmacovigilance , CROs and other vendors to ensure high quality of deliverables to… more
- Takeda Pharmaceuticals (Boston, MA)
- …to the best of my knowledge. **Job Description** **About the role:** Associate Director, Clinical Program Quality Investigations is responsible for ensuring the ... Clinical Program Quality team and share insights to trends to Clinical Pharmacovigilance and Medical Quality and R&D Quality leadership for proactive risk mitigation… more
- Takeda Pharmaceuticals (Boston, MA)
- …CPMQ activities eg audit, inspection, QE, CAPA. + Organise Clinical and Pharmacovigilance Quality council meetings and proactively manage the agenda and ensure key ... include successful development and implementation of a clinical or pharmacovigilance audit program, hosting/leading regulatory inspections, investigations and remediation… more
- AbbVie (North Chicago, IL)
- …to support potential product related issues *Key medical quality interface with Pharmacovigilance & Patient Safety (PSEQ), Global Medical Affairs (GMA) and Clinical ... device/ combination product vigilance (safety signal detection, data mining techniques, pharmacovigilance / device vigilance databases, etc.) + Track record of… more
- Amgen (Washington, DC)
- …experience in a hospital, university or clinical research unit setting **Or** Associate 's degree (ADN) and 10 years of Safety/ Pharmacovigilance or Clinical ... degree (PhD or DNP) OR PharmD OR MD and 2 years of Safety/ Pharmacovigilance or Clinical Research experience in a hospital, university or clinical research unit… more
- Lilly (Indianapolis, IN)
- …to make life better for people around the world. The purpose of the Associate /Senior Associate /Principal Associate - MQO is to support the development ... + Understand the roles and responsibilities of the EU Qualified Person for Pharmacovigilance (EU QPPV), if applicable. + Serve as an IT systems business quality… more
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