Senior Manager/Director of Regulatory Affairs
3 weeks ago
Regulatory Affairs Manager
This organization has a strong pipeline and portfolio across multiple therapeutic areas, and they are seeking a Regulatory Affairs Manager to join their European General Medicine Regulatory team.
#You’ll provide regional regulatory expertise, guiding strategies and submissions that shape the future of their portfolio.
Plan and manage regulatory submissions for clinical trials and marketing applications.
Implement product-related regulatory strategies in line with national legislation.
Provide guidance on regional regulatory mechanisms (e.g., Conduct regulatory research, monitor evolving legislation, and assess competitor labelling.
#Scientific degree with proven experience in a regulatory role.
Understanding of drug development and the regional regulatory environment.
Planet Pharma is an American parented Employment Business/Agency that provides global staffing services with its head-quarters in Chicago and our EMEA regional office located in Central London. We have invested significantly in creating a robust international platform that enables us to work compliantly in 30+ countries with a current network of 2500+ active contractors globally as well as a very strong permanent / direct hire recruitment offering.
Our specialist knowledge and close relationships with our clients and the wider industry really makes us unique in our field. Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs / Writing.
We are an equal opportunities Recruitment Business and Agency. We welcome applications from all suitably qualified candidates regardless of their race, sex, disability, religion/belief, sexual orientation or age.
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