At a Glance
- Tasks: Write and edit clinical and regulatory documents for a leading pharmaceutical client.
- Company: Join ProPharma, a top-tier company in the pharmaceutical industry.
- Benefits: Competitive salary, flexible working options, and opportunities for professional growth.
- Other info: Collaborative environment with mentorship opportunities for junior writers.
- Why this job: Make a real impact in healthcare by ensuring quality and compliance in medical writing.
- Qualifications: Experience in early phase medical writing and strong communication skills.
The predicted salary is between 60000 - 72000 £ per year.
Pro Pharma is seeking a Senior or Principal Medical Writer with proven early phase experience to support a top‑tier pharmaceutical client.
Based in the UK or Ireland, you will author and edit clinical, safety and regulatory documents across multiple programs, ensuring quality, accuracy and timely delivery.
You will lead project communications, coordinate with cross‑functional teams, mentor junior writers, and maintain compliance with ICH guidelines, FDA expectations, and client templates.
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Senior Medical Writer — Clinical & Regulatory Leader employer: ProPharma
ProPharma is an exceptional employer that fosters a dynamic and collaborative work culture, ideal for those looking to thrive in the fast-paced world of commercial finance. Employees benefit from comprehensive professional development opportunities, working alongside industry leaders while contributing to impactful projects. Located in a vibrant area, ProPharma offers a unique blend of career growth and a supportive environment, making it a rewarding place to advance your career.
