Medical Writing Director for Clinical Trials
3 weeks ago
We are seeking a highly experienced Medical Writing Director to lead our clinical trials team. This role will be responsible for overseeing the preparation of high-quality regulatory submissions and medical writing deliverables.
Key Responsibilities:- Liaise with internal teams and external sponsors to ensure strategic advice and guidance on regulatory affairs and medical writing.
- Manage the entire process, from preparing documentation to maintaining quality and consistency across all submissions.
- Mentor and develop junior staff, while continuously updating SOPs and document templates to reflect the latest regulatory guidelines.
Barrington James is a leading organisation in the clinical trials space, specialising in early-phase studies for pharmaceutical and biotechnology sponsors.
Benefits:- Competitive salary: £80,000 - £120,000 per annum (dependent on experience)
- Private medical insurance, private dental insurance, pension scheme, 25 days annual leave plus bank holidays
We are looking for an experienced professional with at least 5 years of proven experience in medical writing and regulatory submissions. Postgraduate qualification in a relevant scientific, medical, or life sciences field is required.
- Proven experience in submissions for Phase I-III clinical trials
- Experience in mentoring and developing junior staff
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