Associate, Pharmacovigilance Operations/Drug Safety
Orca Bio
WorldwideFully remoteFull TimeJuniorHealthcare & Telemedicine
No salary statedPosted 14 days ago2w agoApply link checked 24 minutes ago
Why we think you can apply
- Hiring model
- Open worldwide · the employer states no country restriction
- Work from
- Anywhere, the UAE included
Posted 14 days ago · apply link checked 24 minutes ago
About the role
Responsibilities
- 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
What we look for
- Reviewing adverse events
- Assisting in regulatory reporting
- Collaboration with functional groups
PharmacovigilanceDrug SafetyClinical Operations
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Orca Bio
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NeverApply scores every new listing against your CV, salary floor and visa. A handful of real matches by morning.
Get your daily matchesAssociate, Pharmacovigilance Operations/Drug SafetyOrca Bio · 3 free applies a month