- Parexel (Olympia, WA)
- …basic training in clinical medicine (residency, internship etc.) This role offers the flexibility to work from home in either the US or Canada. \#LI-LB1 ... comprehensive medical reviews, provide expert safety monitoring, and deliver pharmacovigilance guidance across assigned projects. You'll also mentor junior team… more
- Sanofi Group (Cambridge, MA)
- …that could turn the impossible into possible for millions. The Patient Safety & Pharmacovigilance (PSPV) aspiration is to be a cutting-age safety group, to enable us ... our patients and consumers. The Quality Documents Expert is part of the Pharmacovigilance Quality (PVQ) department in PSPV function working in an international and… more
- Bristol Myers Squibb (Pittsburgh, PA)
- …your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career. **Compensation Overview:** Field - ... key scientific updates to internal stakeholders (eg Commercial, Regulatory, Pharmacovigilance , Legal, HEOR, Value Access & Payment) + Provide...your area. If you live in or expect to work from Los Angeles County if hired… more
- Astellas Pharma (Northbrook, IL)
- …allowing time to connect with colleagues at the office with the flexibility to also work from home . We believe this will optimize the most productive ... our website at www.astellas.com . This position is based in Northbrook, Illinois. Hybrid work from certain states may be permitted in accordance with Astellas'… more
- Astellas Pharma (Northbrook, IL)
- …allowing time to connect with colleagues at the office with the flexibility to also work from home . We believe this will optimize the most productive ... our website at www.astellas.com . This position is based in Northbrook, Illinois. Hybrid work from certain states may be permitted in accordance with Astellas'… more
- Sanofi Group (Morristown, NJ)
- …(SMM) responsibilities eg: leading or contributing to key study documents and activities from clinical development plans and trial set-up to clinical study report in ... team developing a molecular entity, provide input to the clinical development plan, work on the development of the clinical trial protocol, clinical trial materials,… more
- Sanofi Group (Cambridge, MA)
- …the therapeutic area project teams and cross-functional Translational Medicine Subteam from preclinical development through post-marketing. A key focus of this role ... is the path from the research phase through early clinical development including...Managers and Data Managers), Regulatory Affairs, Patients Safety & Pharmacovigilance , Therapeutic Area Research & Development Groups. + External… more
- Sanofi Group (Cambridge, MA)
- …safety input into development plans + Support due diligence activities and pharmacovigilance agreements **Impact:** + Ongoing assessment of the safety status of the ... and labeling + Review, preparation, and/or contribution to questions/requests from health authorities, ethics committees/ IRBs, external partners + Management… more
- Sanofi Group (Cambridge, MA)
- …safety input into development plans + Support due diligence activities and pharmacovigilance agreements **Impact:** + Ongoing assessment of the safety status of the ... safety, and labeling + Review, preparation, and/or contribution to questions from health authorities, ethics committees, IRBs, external partners + Management of… more
- Sanofi Group (Morristown, NJ)
- …input into development plans + Support due diligence activities and pharmacovigilance agreements **Signal Detection & Assessment** + Responsible for signal detection ... Excellent clinical judgment + Capability to synthesize and critically analyze data from multiple sources + Ability to communicate complex clinical issues and… more
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