- Takeda Pharmaceuticals (Boston, MA)
- …adequate training support to all functional areas within Patient Safety & Pharmacovigilance (PSPV) in a Pharmacovigilance (PV) regulated environment. + Supports ... of 5 years prior experience in pharmaceutical industry in a drug safety/ pharmacovigilance global setting + Experience in developing procedural documents and training… more
- Sumitomo Pharma (Boston, MA)
- …seeking a dynamic, highly motivated, and experienced individual for the position of ** Associate Medical Director .** The Associate Medical Director ... + Knowledge of ICH, US & EU regulations, and requirements for Pharmacovigilance . + Excellent interpersonal skills, with demonstrated ability to work in a… more
- United Therapeutics (Boston, MA)
- …You are passionate about PV and enjoy being part of a collaborative team. The Associate Global PV Case Management Director plays a key role in management and ... role is critical in ensuring that commercial operational aspects of pharmacovigilance activities are managed with rigorous global standards in proper documentation,… more
- Takeda Pharmaceuticals (Boston, MA)
- …you and empower you to shine? Join us as a PV Risk Management Scientist/ Associate Director . At Takeda, we are transforming the pharmaceutical industry through ... strive for excellence in everything we do. As an Associate Director / PV Risk Management Scientist, being...Affairs, Biostats) to ensure alignment of global position for pharmacovigilance risk management processes to maximize patient safety +… more
- Rhythm Pharmaceuticals (Boston, MA)
- …barriers, together. Opportunity Overview Rhythm seeks an experienced and highly motivated Associate Director of Medical Writing (MW) who can independently ... + Ensure accuracy and consistency across clinical, medical, regulatory and pharmacovigilance documents, providing expert review of study and program-level documents… more
- 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 ... compliance teams for regulations impacting Clinical, Safety and Clinical Pharmacovigilance Medical Quality (CPMQ) processes and procedures and determined by… more
- Takeda Pharmaceuticals (Boston, MA)
- …true to the best of my knowledge. **Job Description** **About the role:** Associate Director , Clinical Program Quality Investigations is responsible for ensuring ... 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
- Takeda Pharmaceuticals (Cambridge, MA)
- …that will inspire you and empower you to shine? Join us as an Associate Medical Director , Clinical Science in our Gastrointestinal & Inflammation Therapeutic ... a vital contributor to our inspiring, bold mission **POSITION OBJECTIVES:** The Associate Medical Director leads and drives strategy for the overall global… more
- Takeda Pharmaceuticals (Boston, MA)
- …**The Global Category Manager (GCM) - Clinical Development Services Procurement at the Associate Director level, plans and leads category projects for a clearly ... or buying of Compliance Services categories, including but not limited to pharmacovigilance services.** You will be assigned to support Takeda's Research &… more