FSP Medical Writer – Clinical & Regulatory Writing Jobs in Bangalore | Thermo Fisher Scientific | Remote Opportunity
Job Title: FSP Medical Writer
Company: Thermo Fisher Scientific
Division: PPD Clinical Research Services
Location: Bangalore
Job Type: Full-Time
Work Mode: Fully Remote
Industry: Clinical Research / Medical Writing / Pharmaceutical Services
Experience Required: 2+ Years
Eligibility: Life Sciences, Pharmacy, Biotechnology, Medical, or Scientific Graduates/Postgraduates
About the Company
Thermo Fisher Scientific is one of the world’s leading organizations in scientific research, healthcare innovation, and clinical development services. Through its PPD Clinical Research portfolio, the company supports pharmaceutical, biotechnology, and healthcare organizations in accelerating drug development and delivering life-changing therapies globally.
With clinical trials conducted across 100+ countries, Thermo Fisher Scientific continues to lead innovation in decentralized clinical trials, regulatory documentation, and AI-enabled scientific communication.
Job Overview
Thermo Fisher Scientific is hiring experienced professionals for the position of FSP Medical Writer within its expanding Medical Writing Functional Service Provider (FSP) team in India. This opportunity is ideal for candidates with strong expertise in regulatory writing, clinical documentation, and pharmaceutical or CRO environments.
Candidates with exposure to structured content authoring systems, AI-driven content creation, and automated medical writing workflows will have an added advantage.
Key Responsibilities
Write, edit, and review high-quality clinical and regulatory documents
Prepare documents including:
Clinical Study Reports (CSRs)
Clinical Protocols
Investigator Brochures (IBs)
Regulatory Submission Documents
Collaborate with cross-functional clinical and regulatory teams
Ensure all documentation complies with global regulatory guidelines and internal quality standards
Contribute to document structure, formatting, scientific accuracy, and presentation
Review documents prepared by junior writers or team members
Manage project timelines and submission deliverables
Stay updated with global medical writing trends, regulatory requirements, and industry best practices
Educational Qualification
Bachelor’s Degree in:
Pharmacy
Life Sciences
Biotechnology
Medicine
Related Scientific Discipline
Advanced degree preferred
Experience Required
Minimum 2+ years of Medical Writing or Regulatory Writing experience
Prior experience in:
Pharmaceutical Industry
CRO Industry
Clinical Research Organizations
Experience in safety writing such as DSUR preparation will be advantageous
Exposure to:
Structured Content Management Systems
AI-assisted Content Creation
Natural Language Generation tools preferred
Freshers are not eligible for this role.
Required Skills
Strong clinical and regulatory writing expertise
Excellent written and verbal communication skills
Knowledge of global drug development processes and regulatory guidelines
Strong project management and organizational abilities
Ability to work independently and manage multiple deliverables
Leadership and mentoring capabilities
Attention to detail with high-quality compliance standards
Adaptability and problem-solving mindset
Why Join Thermo Fisher Scientific?
Opportunity to work with one of the world’s leading CRO organizations
Exposure to global clinical trials and international regulatory projects
Flexible and remote working environment
Strong learning and development programs
Career growth in clinical research and regulatory affairs
Collaborative global work culture
Competitive compensation and employee wellness benefits
Preferred Keywords for Job Seekers
Medical Writer Jobs in Bangalore, Clinical Regulatory Writer Jobs India, Remote Medical Writing Jobs, Pharmacovigilance Writing Careers, CRO Medical Writer Vacancy, Clinical Study Report Writer Jobs, Regulatory Writing Jobs for Pharma Professionals, Thermo Fisher Scientific Careers, PPD Medical Writing Jobs, Clinical Research Writing Opportunities India
How to Apply
Candidates with experience in medical writing, clinical documentation, regulatory submissions, and CRO operations are encouraged to apply for this exciting remote opportunity with Thermo Fisher Scientific.
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