German and French Speaking Pharmacovigilance Associate
2 dni temu
Job Summary
Pfizer is seeking a highly motivated and experienced Drug Safety Surveillance / Pharmacovigilance Associate to join its Worldwide Safety department in Poland-Warsaw.
The successful candidate will be responsible for identifying, assessing, and processing cases, including writing and editing case narratives, to allow the generation of reports and ensure adherence to regulatory compliance timelines.
This role requires a good understanding of pharmacovigilance processes and procedures, as well as excellent communication and problem-solving skills. The ideal candidate will have a solid understanding of regulatory compliance and be able to work effectively in a team environment.
Responsibilities
- Select routine cases for processing and determine the appropriate prioritization criteria.
- Review and rank cases to assess their complexity and identify areas requiring proper escalation.
- Collaborate with quality lines and relevant project team subject matter experts to ensure the accuracy and quality of information presented in assigned cases.
- Identify potential areas for process improvements and communicate these to line management.
Requirements
- Bachelor's degree in a science-related field, Pharmacy, or equivalent.
- Experience in pharmacovigilance, regulatory, or in clinical or scientific research is an advantage but not a requirement.
- Fluent English comprehension, reading, and speaking skills (B2 or higher), and German or French (B2 or higher) is a requirement.
- Ability to manage data in a Safety database (Argus preferred) is an advantage but not a requirement.
- Microsoft Office competent user (mainly Word, PowerPoint, Excel).
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Warszawa, Mazovia, Polska Pfizer Pełny etatAbout the RolePfizer is excited to present an opening for an enthusiastic, talented, dynamic international-minded individual to join its Worldwide Safety department as a Drug Safety Surveillance / Pharmacovigilance Associate.The successful candidate will be responsible for reviewing, preparing, and completing individual case safety reports of adverse drug...
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