Senior Associate, Aggregate Reporting Physician
ClinChoice · Erevan
Job description
About the role
ClinChoice is seeking a Senior Associate, Aggregate Reporting Physician to join its in‑house team on a permanent basis. The role focuses on creating high‑quality safety and pharmacovigilance documents that support the surveillance and regulatory compliance of consumer health products.
Key responsibilities
- Prepare, review, and maintain pharmacovigilance and risk‑management documents for consumer health products.
- Synthesize safety information from individual case safety reports, aggregate data analyses, clinical trial safety data, post‑marketing surveillance, epidemiology studies, literature, and signal‑detection activities.
- Draft and support Periodic Safety Update Reports (PSURs/PBRERs/PADERs), Development Safety Update Reports (DSURs), ad‑hoc safety reports, signal assessment reports, and risk‑management documentation.
- Collaborate with Safety Scientists, Medical Reviewers, Drug Safety, Medical Affairs, Regulatory Affairs, Clinical Development, Quality, and R&D teams to evaluate emerging safety information.
- Assist in interpreting safety trends, potential signals, and benefit‑risk considerations.
- Support literature surveillance and summarize relevant safety findings.
- Ensure all documents comply with global pharmacovigilance regulations, company SOPs, and applicable guidance.
Required profile
- Experience in pharmacovigilance and safety data synthesis for consumer health products.
- Familiarity with regulatory submission requirements and risk‑management processes.
- Ability to work collaboratively across multidisciplinary teams.
Required skills
What we offer
- Professional development opportunities within a global CRO.
- Collaborative "one‑team" culture focused on work‑life balance.
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Published 1 month ago
Expires 3 weeks from now
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ClinChoice
Erevan
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