At a Glance
- Tasks: Lead the creation of regulatory documents and manage complex submissions.
- Company: GSK, a global leader in healthcare innovation.
- Benefits: Hybrid work model, relocation support, and a focus on professional growth.
- Other info: Join a diverse team dedicated to high-quality standards and collaboration.
- Why this job: Make a significant impact in healthcare while working in a supportive environment.
- Qualifications: PhD-level expertise in medical writing and regulatory compliance.
The predicted salary is between 51750 - 63250 £ per year.
GSK in Stevenage is seeking a Ph D‑level Regulatory Medical Writer to author and manage CTD submissions, protocols, CSRs and Investigator’s Brochures.
You will lead complex dossiers, ensure compliance with ICH/GCP, and partner across global teams to reflect clinical and statistical data in regulatory narratives.
Hybrid work with ongoing relocation planning to Cambridge, and a focus on delivering high‑quality regulatory documents while growing within a supportive, inclusive environment.
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Senior Medical Writer - Regulatory Dossier Lead in Stevenage employer: GlaxoSmithKline
GlaxoSmithKline is an exceptional employer, offering a dynamic work environment that fosters innovation and collaboration in the pharmaceutical industry. With a strong commitment to employee development, you will have access to numerous growth opportunities while enjoying a competitive salary, annual bonus, and a flexible hybrid working model that promotes work-life balance. Located in the UK, GSK's culture prioritises teamwork and inclusivity, making it a rewarding place for professionals passionate about making a difference in healthcare.
