Apply for Principal Medical Writer job at Fortrea 2026. Check eligibility, leadership experience, and clinical writing role details online now today.
Introduction
Medical writing is a critical function in clinical research, ensuring accurate communication of scientific data to regulatory authorities and stakeholders. The Principal Medical Writer Job at Fortrea is an excellent opportunity for experienced professionals to lead complex writing projects and contribute to global clinical development programs.
This role is ideal for senior medical writers who want to take leadership responsibilities while working on high-impact clinical and regulatory documents.
Job Overview
| Particulars | Details |
|---|---|
| Job Title | Principal Medical Writer |
| Company Name | Fortrea |
| Location | Pune, India |
| Employment Type | Full-Time |
| Department | Medical Writing |
| Experience Required | 8+ Years |
| Education | Life Sciences Degree (PhD/Master’s Preferred) |
| Salary | As per company norms |
Company Overview
Fortrea is a leading global Contract Research Organization (CRO) delivering clinical development, data, and regulatory services to pharmaceutical and biotechnology companies.
With a strong global presence and expertise in clinical trials, Fortrea focuses on innovation, quality, and scientific excellence to support drug development across all phases.
Job Location & Employment Type
This is a full-time position based in Pune, India. The role may require occasional travel for client meetings, conferences, and project collaborations.
Open Positions / Department Details
The role is part of the Medical Writing team, responsible for preparing high-quality clinical and regulatory documents across early and late phases of clinical development.
Key Roles & Responsibilities
- Lead the development of complex clinical documents such as:
- Clinical Study Protocols
- Clinical Study Reports (CSRs)
- Investigator Brochures (IB)
- CTD Module 2 documents
- Coordinate large-scale writing projects involving multiple deliverables
- Perform scientific review of protocols, statistical plans, and study reports
- Ensure accuracy, consistency, and regulatory compliance of all documents
- Prepare submission-level regulatory documents
- Develop scientific publications, abstracts, posters, and manuscripts
- Act as a liaison between clients and internal teams
- Provide leadership, mentoring, and training to medical writers
- Contribute to business development activities and client presentations
- Support audits and regulatory inspections
- Drive process improvements and adoption of new technologies
- Ensure timely delivery of high-quality documents
Eligibility Criteria
Education
- Bachelor’s degree in Life Sciences or equivalent
- Master’s or PhD preferred
Experience
- Minimum 8+ years of medical writing experience
- At least 3 years as a medical writing project lead
Skills Required
- Strong knowledge of clinical development and regulatory processes
- Expertise in ICH guidelines and regulatory requirements
- Excellent scientific writing and data interpretation skills
- Advanced knowledge of medical terminology
- Strong leadership and project management abilities
- Excellent communication and stakeholder management skills
- Proficiency in MS Word and document preparation tools
Salary & Benefits
- Salary: As per company norms
- Opportunity to lead global clinical writing projects
- Exposure to international regulatory submissions
- Career growth in leadership roles
- Professional development and training programs
- Collaborative and research-driven work environment
Selection Process
The hiring process generally includes:
- Resume screening
- Technical interview (medical writing & regulatory knowledge)
- Managerial/leadership interview
- HR discussion
- Final selection
How to Apply
Candidates can apply through the official online application portal. Ensure your resume highlights your experience in medical writing, leadership roles, and regulatory documentation.
Important Dates
- Last Date to Apply: April 15, 2026
Why Apply for This Job?
The Principal Medical Writer Job at Fortrea offers a senior-level opportunity to lead critical clinical documentation projects and influence global drug development.
Key benefits include:
- Leadership role in medical writing
- Work on complex clinical and regulatory documents
- Exposure to global pharmaceutical clients
- Opportunity to mentor and guide teams
- Strong career growth in clinical research and regulatory writing
This role is ideal for experienced professionals aiming to advance into leadership positions in medical writing and clinical development.
FAQs
1. What is the eligibility for Principal Medical Writer Job at Fortrea?
Candidates must have a life sciences degree with 8+ years of medical writing experience.
2. Is leadership experience required?
Yes, at least 3 years of experience as a project lead is required.
3. What documents will I work on?
You will work on protocols, CSRs, CTD documents, and scientific publications.
4. What is the job location?
The job is based in Pune, India.
5. What is the last date to apply?
The last date to apply is April 15, 2026.
Conclusion
The Principal Medical Writer Job at Fortrea 2026 is a premium opportunity for experienced professionals to take on leadership roles in clinical writing. With global exposure, high-impact projects, and strong career growth, this position is ideal for advancing in the medical writing domain.
Apply soon to secure your position in this competitive role.
Disclaimer
IndiaPharmaJobs.in is an independent job information platform. We do not provide jobs or recruitment and are not affiliated with any company.
