Posted to MedZilla on 8/20/2017


England, Associate Director, Regulatory Affairs RA_AC_12994-MZ


ProClinical is currently working with a well-established pharmaceutical development organisation who are seeking an Associate Director of Regulatory Affairs to work on their pharmaceutical and biotech projects. They are growing in size and are looking to develop their RA function further.

The AD of RA will act as a lead on a number of technical projects and will focus on a range of activities including:

  • Submission of Clinical Trial Applications, ODDs, PIPs, MAA's, Post approval changes
  • Management of complex projects and liaising with health authorities
  • People management of internal/external contractors and partners
  • Input into Regulatory strategy

The ideal candidate will have a broad skill set covering pre-and post approval Regulatory Affairs. Being in an emerging organisation, candidates should have demonstrable experience in pharma/biotech/CRO with proven ability to work under their own initiative.

NB: Applicants should also be eligible to work in the UK.

To Apply:

Please click on the Apply button. Please include a short note outlining why you are interested in the role and why you think you are suitable.
In case you have difficulty in applying or if you have any questions, please call Alex Czuprynski on +44 203 8692 328 or upload your CV on our website -
A full job description is available on request.
ProClinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies. 

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* If a direct employer requests that you go to their web site and complete your application there in order to be
  considered, please do so. Applications for all positions are subject to each employer's specific requirements.