Senior Medical Writer - Non-clinical

Thermo Fisher Scientific UK

United Kingdom
Competitive salary; benefits: extensive health + w...
Fully remote
5+ years medical writing experience
Author clinical study reports and protocols
Write complex regulatory documents like inds and maas
The role involves providing high-quality medical and scientific writing for internal and external clients within a Functional Service Partnership team

Job Summary

  • The role involves providing high-quality medical and scientific writing for internal and external clients within a Functional Service Partnership team.
  • Candidates must possess the versatility to author both clinical and preclinical regulatory documents with specific expertise in infectious diseases or oncology.
  • The company offers an award-winning learning and development program, competitive salary, and a flexible working culture that values work-life balance.

Matching Summary

The role involves providing high-quality medical and scientific writing for internal and external clients within a Functional Service Partnership team.

Salary

Competitive salary; Benefits: extensive health and well-being package; Not specified

Skills & Requirements

Must-have

  • 5+ years medical writing experience
  • Author clinical study reports and protocols
  • Write complex regulatory documents like INDs and MAAs
  • Expertise in infectious diseases or oncology
  • Strong data interpretation and proofreading skills

Nice-to-have

  • Experience working in client-dedicated CRO roles
  • AMWA, EMWA, or RAC certifications
  • Mentorship and training capabilities
  • Program management and budget forecasting skills
  • Collaborative global team environment

Key Requirements

  • Bachelor's degree in scientific field (Advanced preferred)
  • 5+ years of relevant medical writing experience
  • Previous pharmaceutical or CRO industry experience
  • Knowledge of global document development guidelines

Work Rights

Not specified

Tailored Resume

Cover Letter