Job Title: Senior Manager, CTA Regulatory Strategy Location: Remote (UK or Germany) Employment Type: Full-time, Permanent Were partnering with a leading global pharmaceutical organisation to identify an experienced Senior Manager, CTA Regulatory Strategy to support the
The FTE Medical Writer will serve as an integrated member of the team, delivering medical writing services for the development of clinical documents, including Clinical Trial Reports (CTRs), Trial Design Outlines/Clinical Trial Protocols (TDOs/CTPs) and CTP amendments, Briefing Books, Investigator’s Brochures (IBs) and
Senior Manager, CTA Regulatory Strategy | EU & UK We’re looking for an experienced Senior Manager, CTA Regulatory Strategy to play a key role in shaping and executing global regulatory strategy for clinical trial applications. This
Role: Regulatory Associate – CTA Contract: 12-month rolling Office- Maidenhead (hybrid) – 3 days on site SRG are partnered with a global biopharmaceutical company with focus and capabilities to address some of the world’s greatest health
Regulatory Consultant – Clinical Trial Strategy & Submissions Location: Maidenhead - 3 days a week on site – Tues, Wed, Thurs Contract: 12 months We are currently seeking an experienced Regulatory Consultant to join a Clinical
IQVIA in Frankfurt/Main is seeking an FTE Medical Writer to deliver high-quality clinical documents for regulatory submissions, including CTRs, IBs, and CTP amendments, with a focus on eye health and inflammation. The FTE Medical Writer will work
Frankfurt/Main, Germany | Full time | Hybrid | R The FTE Medical Writer will serve as an integrated member of the team, delivering medical writing services for the development of clinical documents, including Clinical Trial Reports