Regulatory Affairs Strategist

Job Details

A global, leading Pharmaceutical company are looking to bring on a Regulatory Affairs Strategist to their team, to be based at their office in Kent, ideally with French speaking skills.

Role:
- To manage projects and product-related registration strategies.
- Single point of contact for worldwide RA strategy
- Interpretation of regulatory requirements to the drug development process, including promulgation of health authority marketing authorisation dossiers.
- Partners with relevant functional teams, including Global Chemistry Manufacturing and Control, Commercial, Business and Development, Global Manufacturing, and Worldwide Regulatory Operations.
- Preparation and submissions for Module 1, Marketing Authorisations and Variations.
- Clinical, labelling, project management, development and scientific advice.
- Provide input to the regulatory strategy for the development of products.

Experience and Qualifications:

- Scientific degree
- Beneficial to have French speaking skills.
- 2 - 4 years Regulatory Affairs experience.
- Project management skills.

To Apply:

To apply, please click on the Apply button. Ideally, 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 me (Elise Lambeth) on +44 (0) 207 440 0633 or upload your CV on our website. Full description available on request.

Please note that not all of our vacancies are advertised. To register as a priority candidate, please upload your CV on our website with a short description of what you are looking for or call 0800 988 4437. We will then contact you with relevant roles: www.proclinical.co.uk. We regard all correspondence as confidential.

Proclinical is a specialist Employment Agency and Recruitment Business, providing employment opportunities within major companies in the Pharmaceutical and Biopharmaceutical industries across Europe.