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Pharmacovigilance Trainee Position
Il y a 3 mois
Key Responsibilities:
- Document and maintain records of adverse events within the pharmacovigilance database.
- Enhance data integrity by identifying duplicates and confirming the accuracy of information.
- Oversee departmental email correspondence with partners and distributors.
- Engage in the search and importation of adverse event reports.
- Support the testing and validation processes of the new pharmacovigilance database.
- Perform literature reviews and compose technical documentation.
Qualifications:
- Currently enrolled in veterinary studies, pharmacy (Master 1/2), pharmacology engineering, or life sciences with a specialization in the pharmaceutical sector (Master 1/2).
- Fluent in both French and English.
Benefits Offered:
- Attractive salary and comprehensive benefits package.
- Opportunities for career advancement and skill development.
