Line Manager - Regulatory Submissions
Permanent, Full-Time, Office-Based role
Extremely competitive basic salary + excellent benefits package
Multiple Locations available: Madrid; Lyon; Munich.
Following a period of rapid growth, our client (Global CRO) is undergoing heavy expansion and they are currently looking for skilled industry professionals to take on a leading role within their Regulatory Affair departments across key central Europe locations.Specifically, they are looking for Line Managers to guide the strategy and the development of the local and regional teams of Regulatory Submissions Coordinators. The Line Manager of Regulatory Submissions will be responsible for the single teams and will have an impact on the Clinical Studies on a project basis.
Further responsibilities include:
- Ensure consistent communication with research sites regarding the distribution and review of site essential documentation is kept across the team;
- Assess and oversee quality reviews of Trial Master File (TMF);
- Be responsible for the overall regulatory start-up submissions process;
- Ensure all main site start-up timelines are met.
- Provide advice and guidance to internal and external team members to ensure compliance with applicable regulations and requirement
- Life Science or Healthcare related degree;
- Strong experience in Regulatory Submissions department within a CRO environment;
- Proven track record of team(s) Line Management
- Fluent in English and local language (according to location).
WANT TO APPLY?
For an immediate consideration please press 'apply' or alternatively contact Emanuele either via email (email@example.com) or call (+44 0203 910 9516) now and get more information about the role.Our team at SRG Clinical also cover roles in Biometrics, Medical Affairs, Clinical Operations, Medical Information, Pharmacovigilance and Regulatory Affairs so do not hesitate to get in touch.
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