PHARMAFull-time
Principal Medical Writer
APAC (IN)REMOTEPOSTED: 8/13/2026
PHARMAFull-time
HIRING ORGANIZATIONTHERMO FISHER SCIENTIFICLife Sciences / Scientific Instruments / Biotechnology
ROLE DEFINITION & RESPONSIBILITIES
Author, research, and edit complex clinical and regulatory documents including Clinical Study Reports (CSRs), study protocols, Investigator's Brochures (IBs), ICFs, INDs, and MAA submissions.
Provide senior-level review and quality control across routine and complex regulatory medical writing deliverables.
Train, mentor, and guide junior medical writers on regulatory guidelines, therapeutic concepts, and document preparation tools.
Act as subject matter expert to advise internal and external clients on document development strategy, industry best practices, and regulatory standards.
Assist with program management tasks including timeline creation, budget forecasting, out-of-scope identification, and bid defense presentations.
REQUIRED VERIFIED SKILLS
Regulatory Medical Writing
Clinical Study Reports
Study Protocols
Investigator's Brochure
Submissions
AMWA/EMWA Standards
COMPENSATION & REWARDS
Salary: Competitive / Disclosed upon candidate shortlisting
ORGANIZATION CONTEXT & CULTURE
Thermo Fisher Scientific is a global leader in serving science, providing an extensive range of analytical instruments, laboratory equipment, reagents, consumables, software, and services. They partner with pharmaceutical and biotech companies, hospitals, clinical diagnostic labs, universities, research institutions, and government agencies. The company's mission is to enable its customers to make the world healthier, cleaner, and safer.
TEAM SIZE: 130,000+ employees
INDUSTRY: Life Sciences / Scientific Instruments / Biotechnology
RECOMMENDED TRAINING
1/2
READY TO SUBMIT?
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