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Why this grade This listing scored 22/100, which is an F. It lost the most ground on pay transparency. See the breakdown
- Description depth 20 / 20 How much the posting actually says about the work, measured in characters of real text.
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- Pay transparency 0 / 25 A published salary range, worth more than any other single factor because it is what a candidate cannot find out without applying.
-15 Ghost-job penalty — Deducted for signals that this posting may not be a real, currently-open role — staleness, repeated relisting, or talent-pool language.
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The Pharmacovigilance Specialist will be responsible for ensuring the operational delivery of assigned tasks at the project level, with a focus on safety case reporting, processing of safety case report data, and literature screening activities. The role involves communication with the Pharmacovigilance Team Leader and Pharmacovigilance Manager regarding potential risks related to operational delivery, quality standards, client relationships, and the company's reputation, as well as addressing ad hoc project tasks and requirements.
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
Requirements
- 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)
Benefits
- Full remote flexible work
- Professional growth and career opportunities
- International team and environment
Originally posted on Himalayas
Apply for this role Opens himalayas.app — the link as listed; we have not yet verified it is the employer's own page
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Where this listing came from
- 21 Aug 2026 Himalayas first sighting
Seen on 1 board over 0 days.