PPD clinical research services (part of Thermo Fisher Scientific) is expanding its Medical Writing Functional Service Partnership (FSP) Team in India. Two high-demand remote pharma roles are open in Bangalore:
- FSP Document Review Specialist II (APAC)
- FSP Medical Writer
If you are targeting medical writing jobs in India, regulatory document review roles, or CRO medical writer remote positions, this is a strong opportunity with a global clinical research organization.
1️⃣ FSP Document Review Specialist II (APAC) – Fully Remote
Location: Bangalore, India (Remote)
Experience: 2+ years editorial / regulatory review
Industry: Pharmaceutical / CRO
Key Responsibilities
- Review regulatory documents (CSR, IB, protocols, submissions)
- Verify scientific accuracy in tables, listings, and figures
- Ensure compliance with ICH, GCP, FDA, and international guidelines
- Edit for clarity, consistency, grammar, and template adherence
- Query authors for scientific correctness
- Maintain document quality standards in client-dedicated FSP model
Required Qualifications
- Bachelor’s degree in Life Sciences / Pharmacy / related field
- 2+ years editorial experience
- Experience in pharmaceutical/CRO industry preferred
- Knowledge of ICH, FDA guidelines, GCP
- Strong document management system experience
- High English proficiency and scientific understanding
Ideal For
- Regulatory document reviewers
- Scientific editors in CRO
- Clinical document QC professionals
- Medical writing quality specialists
2️⃣ FSP Medical Writer – Fully Remote
Location: Bangalore, India (Remote)
Experience: 2+ years regulatory writing
Industry: Pharmaceutical / CRO
Key Responsibilities
- Write and edit Clinical Study Reports (CSR)
- Develop protocols and Investigator Brochures
- Prepare regulatory submissions
- Support DSUR and safety writing (advantage)
- Collaborate cross-functionally with clinical teams
- Work on structured content authoring systems
- Apply AI-driven content generation tools where applicable
Required Qualifications
- Bachelor’s degree in scientific discipline (Advanced degree preferred)
- 2+ years regulatory medical writing experience
- CRO/pharma industry experience required
- Knowledge of structured content management systems
- Understanding of global regulatory guidelines
Ideal For
- Regulatory Medical Writers
- Clinical Scientific Writers
- DSUR / Safety Writers
- Structured Content Authors in Pharma
💰 Salary (Estimated India Range)
| Role | Expected CTC (INR per annum) |
|---|---|
| Document Review Specialist II | ₹8 – 14 LPA |
| FSP Medical Writer | ₹10 – 18 LPA |
(Based on industry benchmarks for 2–5 years CRO experience in India.)
🌟 Benefits at PPD (Thermo Fisher Scientific)
- Fully Remote Work Model
- Competitive Salary
- Global Client Exposure
- Award-winning Learning & Development
- Work-Life Balance Culture
- International Regulatory Experience
- Career Growth in Medical Writing FSP
🎯 Why This Opportunity Matters
With increasing demand for:
- Medical writing jobs in India
- Remote regulatory writing jobs
- CRO document review roles
- FSP medical writer positions
These openings offer strong career stability and international exposure.
Thermo Fisher conducts clinical trials in 100+ countries, making this a globally aligned role.
📌 How to Apply
Application Link For Document Review Specialist II
Application Link For FSP Medical Writer
