Pharmacovigilance Specialist (Case Processing)
RemoteTurkey
Job Summary
Oversee and manage the workflow of safety case reports, performing triage to assess priority and necessary actions. Review, manage, and file source documentation in compliance with regulatory requirements while processing reports that include SDB data entry, narrative writing, and medical review assessments. Execute quality control checks on data entry and case processing, reconcile reports for consistency, and conduct follow-up activities to manage queries. Prepare line listings to summarize and report on safety case data. Ensure operational delivery of assigned tasks with communication regarding potential risks, quality standards, and client relationships. Full-time remote role in Europe or Turkey requiring a Life Science degree and one year of safety experience.
Required Qualifications
- University degree in Life Science field
- At least 1 year of experience in Safety and Pharmacovigilance within the pharmaceutical or Contract Research Organization (CRO) industry
- Proficiency in both verbal and written local language and English
- Strong expertise with MS Office
- Knowledge of EU GVP modules and applicable global safety regulations (e.g. ICH, FDA reporting requirements)
Desired Qualifications
- Beneficial experience with Veeva Vault Safety system
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