Senior Medical Writer – Regulatory Lead (Remote/Hybrid UK) in Cambridge

Senior Medical Writer – Regulatory Lead (Remote/Hybrid UK) in Cambridge

Cambridge Full-Time 60000 - 80000 Β£ / year (est.) No working from home possible
Trilogy

At a Glance

  • Tasks: Lead the creation of essential regulatory documents for the pharmaceutical industry.
  • Company: Join Trilogy Writing & Consulting, a forward-thinking company in the healthcare sector.
  • Benefits: Enjoy flexible working options, competitive pay, and opportunities for professional growth.
  • Other info: Work remotely or in a hybrid model with a dynamic team.
  • Why this job: Make a significant impact in healthcare by supporting vital regulatory processes.
  • Qualifications: Experience in medical writing and strong collaboration skills are essential.

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

Trilogy Writing & Consulting, an Indegene Company, seeks Senior/Principal Medical Writers to support regulatory documentation for the international pharmaceutical industry.

Roles offer remote, hybrid, or UK in-office arrangements from Cambridge, with UK residence required.

Writers will lead the preparation of protocols, CSRs, CTD modules, Investigator Brochures, and related documents in collaboration with client teams and QC staff.

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Senior Medical Writer – Regulatory Lead (Remote/Hybrid UK) in Cambridge employer: Trilogy

Trilogy Writing & Consulting, an Indegene Company, is an exceptional employer that values innovation and collaboration in the pharmaceutical industry. With flexible remote and hybrid working options from the vibrant city of Cambridge, employees enjoy a supportive work culture that fosters professional growth and development. The company offers unique opportunities to lead impactful projects while contributing to meaningful advancements in healthcare.

Trilogy

Contact Details:

Trilogy Recruitment Team

We think you need these skills to ace Senior Medical Writer – Regulatory Lead (Remote/Hybrid UK) in Cambridge

Regulatory Writing
Protocol Preparation
Clinical Study Reports (CSRs)
Common Technical Document (CTD) Modules
Investigator Brochures
Collaboration Skills
Quality Control (QC) Coordination