Senior Medical Writing and Regulatory Strategist
3 weeks ago
Barrington James is a prominent organisation within the clinical trials sector, focusing on early-phase studies for pharmaceutical and biotechnology clients.
This role offers the opportunity to lead and manage teams within a dynamic, research-driven environment, dedicated to advancing medical innovation and supporting the development of transformative therapies.
Key Responsibilities:
- Lead recruitment efforts for the medical writing team, ensuring clear career progression and succession planning.
- Attend senior leadership pipeline meetings to align upcoming studies with organisational priorities and timelines.
- Monitor team performance, timesheets, and productivity to optimise resource allocation and billing accuracy.
$120,000 - $180,000 per annum
The ideal candidate will have a minimum of 5 years' experience in medical writing and regulatory submissions, along with a postgraduate qualification in a relevant scientific, medical, or life sciences field.
This is an excellent opportunity for a highly skilled professional looking to make a significant impact in the fields of medical writing and regulatory submissions.
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