Pharmacovigilance Specialist, Submissions
ProPharma(1 month ago)
About this role
The Pharmacovigilance Specialist, Submissions at ProPharma supports pharmacovigilance regulatory reporting and submission compliance for biotech, medical device, and pharmaceutical clients using a multi-tenant Argus environment. The role helps ensure adherence to reporting processes, periodic safety reporting requirements, and submission testing to maintain compliance with health authorities and safety partners.
Required Skills
- Argus
- ICSR Submissions
- Periodic Reporting
- Gateway Testing
- Data Migration
- Microsoft Office
- Excel
- Detail-Oriented
- Written Communication
- Teamwork
Qualifications
- Post-Secondary Education
- Life Science Degree Preferred
About ProPharma
propharmagroup.comProPharma helps navigate the complexities of drug development and ensure patient health and safety throughout the product lifecycle.
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