Associate, Medical Writing (PSUR)
ClinChoice(1 month ago)
About this role
This role supports ClinChoice’s pharmacovigilance functions by overseeing the processes related to Periodic Safety Update Reports (PSURs). The position works with cross-functional teams across quality, medical operations, clinical, regulatory affairs, and safety to support timely regulatory safety reporting. It contributes to maintaining organizational and regulatory compliance for marketed products.
Required Skills
- PSUR Coordination
- Stakeholder Communication
- Data Compilation
- Schedule Adherence
- Regulatory Compliance
- Issue Escalation
About ClinChoice
clinchoice.comClinChoice is a full‑service global contract research organization (CRO) that helps accelerate drug and medical device approvals to market. They offer end‑to‑end clinical development, regulatory strategy, and operational support across study design, execution, data management and safety to guide sponsors through all phases of development. With global site networks, therapeutic expertise and data‑driven processes, ClinChoice aims to shorten timelines and reduce risk for development programs. They partner with biotech, pharma and device companies to navigate complex regulatory pathways and bring safer products to patients.
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