Pharmacovigilance and medical information associate
Pierre Fabre group
Employer Active
Posted 6 hrs ago
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Nationality
Any Nationality
Gender
Not Mentioned
Vacancy
1 Vacancy
Job Description
Roles & Responsibilities
Pierre Fabre is the 2nd largest dermo-cosmetics laboratory in the world, the 2nd largest private French pharmaceutical group and the market leader in France for products sold over the counter in pharmacies.
Its portfolio includes several medical franchises and international brands including Pierre Fabre Oncology, Pierre Fabre Dermatology, Eau Thermale Av ne, Klorane, Ducray, Ren Furterer, A-Derma, Naturactive, Pierre Fabre Oral Care.
Established in the Occitanie region since its creation, and manufacturing over 95% of its products in France, the Group employs some 10,000 people worldwide. Its products are distributed in about 130 countries. 86% of the Pierre Fabre Group is held by the Pierre Fabre Foundation, a government-recognized public-interest foundation, while a smaller share is owned by its employees via an employee stock ownership plan.
In 2019, Ecocert Environment assessed the Group s corporate social and environmental responsibility approach in accordance with the ISO 26000 sustainable development standard and awarded it the Excellence level.
Pierre Fabre is recognized as one of the "World's Best Employers 2021" by Forbes. Our group is ranked in the Top 3 in the cosmetics industry and in the Top 10 in the pharmaceutical industry worldwide.
Your mission
Ensure continuous monitoring of the safety profile of products in development and on the market:
- Validate deliverables from vigilance officers -
Continuously monitor and analyze the safety profile and benefit/risk ratio of products, based on information collected in France and internationally
- Review and, where applicable, provide justification for paragraphs concerning product tolerability in trial protocols, investigator brochures, IMPDs, clinical trial reports, and marketing authorization dossiers -
Verify the existence of a local vigilance system
- Draft risk management plans and ensure their dissemination to subsidiaries
- Draft responses to all questions from authorities -
Ensure signal detection activities
- Analyze the impact of regulatory texts
- Update procedures inherent to the activity
- Participate in due diligence
We are convinced that diversity is a source of fulfillment, social balance and complementarity for our employees, which is why our offers are open to all, without restriction.
Company Industry
Department / Functional Area
Keywords
- Pharmacovigilance And Medical Information Associate
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