Principal Medical Writer / Senior Medical Writer

Thermo Fisher Scientific UK

Not specified; not specified; competitive salary +...
**
8+ years regulatory medical writing experience
Authoring clinical study reports and protocols
Managing complex medical writing projects
** Thermo Fisher Scientific is seeking a Principal Medical Writer for their remote team in APAC, focusing on producing high-quality medical and scientific documentation. The role requires significant experience in regulatory medical writing and project management, with opportunities for mentorship and collaboration within a global organization. **

Job Summary

  • The role involves providing high-quality medical and scientific writing from planning through delivery of final drafts to internal and external clients.
  • As a subject matter expert, the Principal Medical Writer will develop best practices, lead process improvement initiatives, and provide training to junior team members.
  • Thermo Fisher Scientific offers an award-winning learning and development programme with a flexible working culture that values work-life balance.

Matching Summary

Match Score: 75

** Thermo Fisher Scientific is seeking a Principal Medical Writer for their remote team in APAC, focusing on producing high-quality medical and scientific documentation. The role requires significant experience in regulatory medical writing and project management, with opportunities for mentorship and collaboration within a global organization. **

Salary

Not specified; Not specified; Competitive salary and extensive benefits package

Skills & Requirements

Must-have

  • 8+ years regulatory medical writing experience
  • Authoring clinical study reports and protocols
  • Managing complex medical writing projects
  • Experience in pharmaceutical or CRO industry
  • Senior level document review capabilities

Nice-to-have

  • Experience in Immunology Oncology or Vaccines
  • Submissions document experience
  • AMWA EMWA or RAC qualifications
  • Backup program manager capability
  • Business development support skills

Key Requirements

  • Bachelor's degree in scientific discipline required
  • Advanced degree preferred
  • 8+ years regulatory MW experience
  • Experience managing complex medical writing projects
  • Pharmaceutical/CRO industry experience required

Work Rights

Not specified

Tailored Resume

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