Parexel, one of the world’s leading Clinical Research Organizations (CROs), is hiring for Medical Writer I and Senior Medical Writer positions in India. These remote opportunities are ideal for life sciences professionals with expertise in clinical research, regulatory documentation, and scientific writing who want to contribute to global drug development programs.
If you’re looking for Medical Writer jobs in India, remote medical writing jobs, or clinical regulatory writing careers, this Parexel recruitment offers an excellent opportunity to work with global pharmaceutical and biotechnology clients while supporting life-changing therapies.
Job Overview
| Details | Information |
|---|---|
| Company | Parexel |
| Job Roles | Medical Writer I, Senior Medical Writer |
| Job Type | Full-Time |
| Work Mode | Remote |
| Location | Bengaluru, India (Remote) |
| Department | Medical Writing |
| Industry | CRO / Clinical Research |
| Posted On | July 31, 2026 |
| Last Date to Apply | August 30, 2026 |
Position 1: Medical Writer I
Key Responsibilities
- Author, edit, and review clinical and regulatory documents.
- Prepare Clinical Study Reports (CSRs), Interim Study Reports, Patient Narratives, Safety Update Reports, and Informed Consent Forms (ICFs).
- Conduct literature searches and scientific reviews.
- Analyze clinical study data and prepare scientific documentation.
- Ensure compliance with ICH-GCP guidelines and regulatory standards.
- Perform document quality checks for consistency and accuracy.
- Collaborate with Clinical Operations, Data Management, Biostatistics, Regulatory Affairs, and Medical Affairs teams.
- Support document review cycles and stakeholder feedback management.
Position 2: Senior Medical Writer
Key Responsibilities
- Author and review Protocols, Clinical Study Reports, Investigator Brochures, Clinical Summaries, Clinical Overviews, Safety Reports, and CTD documents.
- Interpret clinical and statistical data for regulatory submissions.
- Conduct literature reviews and scientific analysis.
- Ensure compliance with FDA, EMA, ICH-GCP, and client requirements.
- Lead cross-functional document review meetings.
- Manage timelines and deliver high-quality regulatory documents.
- Mentor junior medical writers.
- Contribute to SOP improvements and process optimization.
- Serve as Medical Writing representative on project teams.
Required Qualifications
Candidates should possess any of the following:
- B.Pharm
- M.Pharm
- B.Sc Life Sciences
- M.Sc Life Sciences
- Biotechnology
- Pharmacy
- Medicine
- MBBS
- PharmD
- MD
- PhD
- Other relevant healthcare or life sciences degrees
Required Skills
- Clinical and regulatory medical writing
- Clinical Study Reports (CSR)
- Investigator Brochures (IB)
- Patient Narratives
- Clinical Protocol Writing
- CTD Documentation
- Literature Review
- Scientific Writing
- ICH-GCP Guidelines
- FDA & EMA Regulations
- Medical Communication
- Microsoft Word & Excel
- Document Management Systems
- Stakeholder Management
- Cross-functional Collaboration
Preferred Experience
Medical Writer I
- Medical writing or scientific writing experience preferred.
- Experience in CRO, pharmaceutical, biotechnology, healthcare, or medical communications organizations is advantageous.
Senior Medical Writer
- Strong medical writing experience within CRO, pharmaceutical, or biotechnology organizations.
- Experience preparing Protocols, CSRs, Investigator Brochures, Clinical Summaries, Clinical Overviews, and CTD documents.
Why Join Parexel?
- Work remotely from India.
- Global exposure to international clinical trials.
- Opportunity to contribute to innovative therapies.
- Collaborative and inclusive work culture.
- Career growth in medical writing and regulatory affairs.
- Exposure to multinational pharmaceutical clients.
- Learning and development opportunities.
- Competitive compensation and employee benefits.
How to Apply
Application Link For Medical Writer I
Application Link For Senior Medical Writer
