Medical Writer
Thermo Fisher Scientific · Remote
Medical AffairsRemoteFull timeCompany career page
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Role summary
Thermo Fisher Scientific seeks a Medical Writer to produce high-quality scientific documentation for clinical and regulatory purposes. The role involves authoring study reports, protocols, and regulatory submissions while collaborating with internal and external stakeholders in a remote setting based in India.
What they're looking for
- Bachelor's degree in scientific discipline or equivalent qualification
- 3+ years of experience in medical writing or related scientific role
- Pharmaceutical or CRO industry experience preferred
- Strong medical writing, editorial, and proofreading skills
- Knowledge of regulatory documentation and drug development processes
- Proficiency with document management systems and Microsoft Office applications
- Ability to interpret and present complex data accurately and concisely
What you'll be doing
- Author clinical study reports, study protocols, and related regulatory documentation
- Summarize and interpret data from clinical studies for various audiences
- Assist with complex documents including Investigator Brochures, INDs, and Marketing Authorization Applications
- Ensure compliance with quality processes and best practices for assigned deliverables
- Participate in project meetings and represent the department at key review sessions
Privacy & handoff
This role links to Thermo Fisher Scientific's own application system. RoleLantern records your interest and checks the link, but the application happens on the employer's site and status updates may not come back to us. Clicking apply does not mark you as applied automatically.