Pharmacovigilance Medical Writer II
Full-time
Mid-Senior Level
Job Overview
We are looking for a pharmacovigilance medical writer to join our team. The Medical Writer will be responsible for medical writing including:
- PSURs/PBRERs
- PADERs
- ACOs
- DSURs
- RMPs
- QC and review of all written output from the operations team as required
- Supporting the project managers to determine scheduling of the aggregate reports for which they are responsible
- In conjunction with the Quality, Compliance and Training Manager identify areas for improvement and address via training, clarifying changes to SOPs/OGs/templates
- Complete quality documentation of aggregate reports
- Attending kick off meetings with new clients as required
- Attending audits and inspections as required
- Providing aggregate report training