Data Officer
ProductLife GroupTunisiaPubliée le
- CDI
- Junior (1-3 ans)
- Information Technology
- $6,500.00/yr - $9,300.00/yr
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Compétences demandées
- Pharmacovigilance
- Gestion de données
- Triage
- Dossiers de sécurité
Description de l'offre d'emploi
ProductLife Group recrute : Data Officer, Tunisia (CDI).
Position Overview
We are looking for a Pharmacovigilance Data Officer to support our Patient Safety team in managing an increasing volume of pharmacovigilance cases.
The successful candidate will contribute to the triage, assessment, follow-up and data entry of safety cases received from different sources. The role requires strong attention to detail, good organizational skills and the ability to work in a regulated environment.
Main Responsibilities
- Perform the initial triage and assessment of pharmacovigilance cases.
- Process cases received from spontaneous reports, health authorities, scientific literature and other sources.
- Perform pre-data entry and data entry of safety information into the pharmacovigilance database.
- Review available case information and identify missing or incomplete data.
- Prepare and send follow-up requests when additional information is required.
- Update internal Excel trackers and case management tools.
- Complete internal checklists and quality control activities.
- Support CAPA-related checks and follow-up actions.
- Archive case-related documents in accordance with internal procedures.
- Ensure that cases are processed according to applicable timelines, SOPs and work instructions.
- Collaborate with Pharmacovigilance Officers, medical writers, database administrators and other team members.
- Support additional routine pharmacovigilance activities when required.
Education
- University degree in pharmacy, life sciences, biology, healthcare or another relevant scientific field.
- A pharmacy degree would be considered an advantage but is not mandatory.
Required Experience
- At least 6 months to 1 year of experience in pharmacovigilance case management.
- Previous experience in safety data entry, case processing or drug safety activities.
- Understanding of basic pharmacovigilance processes and regulatory reporting timelines.
Language Requirements
- Good professional level of English is required.
- French languag
Annonce repérée sur LinkedIn et réunie par Alzotech. Valable jusqu'au 30 octobre 2026 au plus tard.