Senior Medical Writer – Regulatory Lead (Remote)

Senior Medical Writer – Regulatory Lead (Remote)

Full-Time 60000 - 80000 £ / year (est.) No working from home possible
Meeveem Limited

At a Glance

  • Tasks: Lead the creation of high-quality clinical documents and mentor junior writers.
  • Company: Join Thermo Fisher Scientific, a leader in scientific innovation.
  • Benefits: Enjoy remote work flexibility, competitive salary, and career development opportunities.
  • Other info: Be part of a supportive environment that values your growth.
  • Why this job: Make a real impact in the medical field while working with a dynamic team.
  • Qualifications: Experience in medical writing and strong communication skills required.

The predicted salary is between 60000 - 80000 £ per year.

Thermo Fisher Scientific is expanding its Medical Writing FSP team in Europe, offering a remote Principal Medical Writer position dedicated to a client in the FSP space. The role involves planning, coordinating, and delivering high‑quality clinical documents, with mentoring responsibilities for junior writers. As the lead writer, you will advise on development strategy, ensure regulatory compliance, and collaborate with internal and external clients to enable effective communication.

Senior Medical Writer – Regulatory Lead (Remote) employer: Meeveem Limited

Meeveem Limited is an exceptional employer that values its employees by fostering a collaborative and innovative work culture in the heart of Yorkshire. With a strong focus on professional development, employees are encouraged to grow their skills and advance their careers while enjoying competitive benefits and a supportive environment that prioritises work-life balance. Joining Meeveem means being part of a dynamic team dedicated to making a meaningful impact in the cardiovascular and endovascular sectors.

Meeveem Limited

Contact Details:

Meeveem Limited Recruitment Team

We think you need these skills to ace Senior Medical Writer – Regulatory Lead (Remote)

Medical Writing
Regulatory Compliance
Clinical Document Preparation
Mentoring Skills
Development Strategy
Project Coordination
Effective Communication