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OrcaBio
Full-time
Middle
🇺🇸 USA
🚀 Management
🏠 Remote
Associate, Pharmacovigilance Operations/Drug Safety
Summary: Responsible for reviewing adverse events and assisting in the determination of regulatory reporting for assigned investigational products. May serve as a liaison to internal and external stakeholders for AE reporting issues (i.e. site staff, CRAs, case processing vendor). Works in collaboration with other functional groups such as data management, clinical operations, regulatory affairs, quality, and medical affairs.
Full-time
Employment
Remote
Work Format
Middle
Grade
B2 - Upper-Intermediate
English Level
Other
Specialization
BioTech
Industry
Startup
Company Type
Full-time
Employment
Remote
Work Format
Middle
Grade
B2 - Upper-Intermediate
English Level
Other
Specialization
BioTech
Industry
Startup
Company Type
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