With deep industry knowledge, global reach and a loyal network of talented jobseekers, we can successfully fill permanent and contract life sciences roles anywhere in the world.
This is an excellent opportunity to advance your career and gain exposure to CMC Regulatory Affairs in a varied pipeline of products.
Regulatory Affairs Submissions Specialist required to coordinate regulatory submissions within the EMEA region. The successful candidate will be responsible for the planning, review and submission of regulatory documents.
The desired candidate will have experience with case processing, medical review and ensuring quality control and quality assurance.
Work is an adventure.
And we're here to take you where you want to go.
Whether you’re looking for payroll benchmarking or pre-screening, we can offer you end-to-end and standalone recruitment solutions specially designed for your business.
I'm tenacious, driven, focused on providing direction to help others succeed, highly energetic and fun!
+44 (0)20 7002 0000
Client director - North America
I have over six years' experience developing contingent recruitment strategies for Medical Device, Pharmaceutical & CRO companies across the USA and EMEA.
Client services manager - EMEA
I am a highly experienced recruiter, dedicated to continually making our client relationships and service levels even better.
I manage our contract team in EMEA. This includes defining the ongoing client strategy for the contract practice, expanding our market share as well as contractor growth.
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