At a Glance
- Tasks: Author regulatory and clinical documents while leading quality delivery and timelines.
- Company: ProPharma, a leader in medical writing with a focus on collaboration.
- Benefits: Competitive salary, mentorship opportunities, and a chance to shape the future of healthcare.
- Other info: Join a dynamic team with opportunities for professional growth and development.
- Why this job: Make a real impact in early-phase regulatory writing and guide junior talent.
- Qualifications: 7+ years in clinical/regulatory writing and strong knowledge of FDA guidelines.
ProPharma is seeking a Senior/Principal Medical Writer based in the UK or Ireland. The role focuses on authoring regulatory and clinical documents across phases, with leadership in delivery quality and timelines.
You will collaborate with cross-functional teams and mentor junior writers to maintain high standards. Ideal candidates have 7+ years of clinical/regulatory writing experience, strong knowledge of FDA/regulatory guidelines, and excellent communication and project-management skills.
#J-18808-Ljbffr
Senior/Principal Medical Writer: Early-Phase Regulatory Expert employer: PPG UK ProPharma Group MIS Ltd
PPG UK ProPharma Group MIS Ltd is an excellent employer that values diversity and inclusion, providing a supportive work culture where every team member can thrive. With a strong focus on employee growth opportunities, you will have the chance to enhance your skills while working alongside a dedicated team committed to excellence in clinical research. Located in a vibrant area, the company offers a dynamic environment that fosters collaboration and innovation.
Contact Details:
PPG UK ProPharma Group MIS Ltd Recruitment Team
