Regulatory Writer, senior, consultancy, pharmaceutical, North-West - Successful Regulatory consultancy based in the North-West (close to Manchester) is urgently seeking a Senior Regulatory Writer to join their small yet innovative team. This company are now over 10 years old and were established as part of an umbrella group in order to deal with Regulatory submissions for their high-profile pharmaceutical clients. The right candidate will quickly become integrated as part of a small team, primarily working on producing regulatory documentation within a wide range of therapeutic areas. You will be producing regulatory documentation including clinical study reports, CTD clinical summaries and regulatory response documents. You will also be involved with the following duties:
- Critically reviewing documentation
- Being responsible for monitoring project costs
- Constantly liaising with clients in order to keep them informed on regulatory issues
- Mentoring more junior members of the team
This role would ideally suit someone from a strong pharmaceutical or clinical research regulatory background and from a regulatory writing role. You will have experience in producing high quality documentation to present to clients and regulatory authorities. You must therefore possess excellent communication skills, both oral and written, be ambitious and be able to take the initiative. Any team leading or managerial experience would be advantageous but not essential.
This is a fantastic opportunity to join a world-renowned Regulatory group. This company will not only offer an excellent working environment, but also the help and support you need in order to thrive. This is an URGENT role, so apply today to Charlie Clough on +44 (0)121 616 5067 or email Charlie.clough@paramountrecruitment.co.uk

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