Senior Regulatory Affairs Specialist
3 days ago
Richmond Pharmacology, a leading Contract Research Organisation (CRO), seeks an experienced Senior Regulatory Affairs Specialist to oversee medical writing and regulatory submissions.
Estimated salary: £80,000 - £110,000 per annum.
We are committed to excellence and innovation in early-phase clinical trials for pharmaceutical and biotechnology sponsors. Our teams strive to advance medical research and contribute to the development of life-changing therapies.
This senior role involves managing the entire medical writing and regulatory submissions process, liaising with sponsors, regulatory authorities, and ethics committees. You will be responsible for high-level Quality Control (QC) across all documents, ensuring consistency and regulatory compliance.
The ideal candidate will have at least 5 years of relevant experience and a postgraduate qualification. They will demonstrate excellent scientific writing, editing, and data comprehension skills, as well as advanced knowledge of core scientific principles.
Key responsibilities include:
- Providing strategic guidance on regulatory affairs and medical writing
- Liaising with internal teams and external sponsors
- Mentoring and supervising less experienced team members
As a leader, you will drive the success of projects, foster sponsor satisfaction, and ensure Richmond Pharmacology remains at the forefront of medical writing and regulatory submissions.
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