- Sumitomo Pharma (Boston, MA)
- …a dynamic, highly motivated, and experienced individual for the position of Pharmacovigilance Scientist to perform PV activities for assigned programs(s). Ability to ... to, Clinical Development, Translational Medicine/Early Development, Regulatory Affairs, Data Management and Biostatistics is essential. **Job Duties and Responsibilities**… more
- Sanofi Group (Cambridge, MA)
- …+ Quality focused, able to develop good practices, using a critical data-driven and risk management approach + Ability to work autonomously and efficiently to ... for the clinical studies on activities pertaining to the Study Medical Manager (SMM) responsibilities eg: leading or contributing to key study documents and… more
- Sanofi Group (Cambridge, MA)
- …agencies + Demonstrated capability to challenge decision and status quo with a risk - management approach + Ability to work within a matrix organization, within ... Trial Managers and Data Managers), Regulatory Affairs, Patients Safety & Pharmacovigilance , Therapeutic Area Research & Development Groups. + External contacts:… more
- Parexel (Boston, MA)
- …does not include any direct medical advice on patient care or management + Communicate with relevant sponsor counterparts on challenges and accomplishments related ... actions contributing to the success of the study/project and risk mitigation + Creating a sense of urgency on...Senior Medical Director/ Global Head of TA (as appropriate) Pharmacovigilance Support * Provide medical input into PV workflows… more