Hayden Marsh Pharmaceutical recruit for regulatory roles across the board throughout the UK and Europe. These range from Regulatory Affairs Executives to Senior Regulatory Consultants on a permanent, contract or freelance basis.
In this sector we recruit for roles covering global regulatory affairs, pre and post approval activities, as well as regulatory operations for a number of top pharmaceutical and biotech companies and CRO's. Whether you are involved with clinical regulatory activities i.e. compiling and preparing CTA's and MAA's or post-marketing activities i.e. licence maintenance and managing the product lifecycle, your experience is no doubt highly valuable for our prestigious clients. On a national or international basis, you can boost your career to a consultancy level, providing regulatory expertise to various companies across numerous therapeutic areas, by taking the most prosperous steps up the regulatory ladder with Clinical Professionals.
Our candidates are well-educated in scientific or related disciplines. With many regulatory professionals starting their careers at the MHRA (or respective regulatory authority), our candidates have experience in a variety of regulatory environments, with a good understanding of all aspects of the product lifecycle.
Opportunities in Regulatory include:
- Regulatory Affairs Executive
- Regulatory Affairs Manager
- Regulatory Operations Manager
- Regulatory Submissions Associate
- Regulatory Operations Associate
- Regulatory Consultant
- European Regulatory Director
- Regulatory Manager in Submissions Compliance
- Regulatory Manager in Intelligence and Compliance
Contact pharma@haydenmarsh.co.uk 01865 77 77 33
