Expert in Pharmacovigilance - Belgium - 13-Months
This is a unique opportunity for an Expert in Pharmacovigilance to join our client – an esteemed partner for regulatory and compliance in healthcare. This is a contract opportunity of at least 6 months within the stunning city of Paris. With a globally established presence spanning over countries and partner to some of the top pharmaceutical companies, this is a fantastic company to join to progress your career.
Responsibilities
- Responsible for adverse event management including aggregate and individual case safety report (ICSR) health authority submissions an compliance monitoring
- PV intake
- Management and negotiation of local PV agreements
- Local due diligence activities
- Participation in audits and inspections and related readiness activities
- Review of local initiatives for compliance with PV requirements
- SOP management
- local training
- communication of safety issues
- people development
- special projects as assigned and is able to work on these delegated activities independently
- Working independently yet close together with the team
- Providing guidance and steering to the support in Pharmacovigilance
Job Requirements
3 years of experience in PharmacovigilanceHealth, Life Science, or Medical Science Degree or equivalent experience (ideally within pharmacy)Languages : Fluent in English and DutchFlexibility and Remote wayIf this role is of interest to you, please apply now!
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