Pharmacovigilance Specialist (Case Processing)
Indexed description
CV must be in English language for further assessment.
Position is full-time remote/home-based in any European country and Turkey.
Responsibilities:
- Oversee and manage the workflow of safety case reports, ensuring efficient processing
- Perform triage on safety case reports to assess priority and necessary actions
- Review, manage, and file source documentation in compliance with regulatory requirements
- Process safety case reports, including SDB data entry, narrative writing, seriousness assessment, medical review (including causality and expectedness assessments), and reporting requirements evaluation
- Conduct follow-up activities and manage queries related to safety case reports
- Execute quality control checks on data entry and case processing to ensure accuracy and compliance
- Reconcile safety case reports to ensure consistency and completeness of data
- Prepare line listings to summarize and report on safety case data
- 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
- Experience of clinical trial case processing in a safety database
- Proficiency in both verbal and written local language and English
- Strong expertise with MS Office
- Beneficial experience with Veeva Vault Safety system
- Knowledge of EU GVP modules and applicable global safety regulations (e.g. ICH, FDA reporting requirements)
- Full remote flexible work
- Professional growth and career opportunities
- International team and environment
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