Accutest Research Laboratories (India) Pvt. Ltd. is hiring a Medical Writer – Protocol Writer at its Clinical Pharmacology Unit in Navi Mumbai.
This opportunity is ideal for professionals with 2–4 years of experience in clinical research, regulatory writing, and protocol development. With rising demand for clinical trial documentation, regulatory submissions, and CRO services, medical writing roles are among the fastest-growing careers in the pharmaceutical industry.
Company Overview
Accutest Research Laboratories (I) Pvt. Ltd. is a reputed Contract Research Organization (CRO) specializing in clinical research, bioequivalence studies, and regulatory support.
The company supports global pharmaceutical clients with ICH-GCP compliant documentation, clinical trials, and regulatory submissions, making it a strong platform for career growth in medical writing and regulatory affairs.
Job Role: Medical Writer (Protocol Writer)
As a Medical Writer – Protocol Writer, you will play a critical role in preparing and managing clinical trial protocols and regulatory documents.
Key Responsibilities
- Develop and write clinical trial protocols as per regulatory guidelines
- Collaborate with clinical operations and regulatory affairs teams
- Ensure accuracy, clarity, and scientific integrity in documents
- Review and edit protocols for consistency and compliance
- Support preparation of regulatory submission documents
- Maintain documentation as per ICH-GCP guidelines and SOPs
- Update and manage protocol templates and writing standards
Eligibility Criteria
Educational Qualification
- B.Pharm
- B.Sc (Life Sciences / Biotechnology / Microbiology / Biochemistry)
Experience
- 2 to 4 years in medical writing or clinical research
Skills Required
- Strong knowledge of clinical trial protocols
- Understanding of ICH-GCP guidelines
- Excellent scientific writing and documentation skills
- High attention to detail and analytical ability
- Strong communication and coordination skills
Job Location & Salary
- Location: Koperkhairane, Navi Mumbai
- Salary: ₹4.5 LPA – ₹7.5 LPA (Estimated, based on industry standards)
- Preference: Immediate joiners preferred
Benefits of Working at Accutest
- Exposure to global clinical trials and regulatory submissions
- Opportunity to work in a leading CRO environment
- Career growth in medical writing and regulatory affairs
- Hands-on experience with ICH-GCP compliant documentation
- Collaborative and research-driven work culture
How to Apply
Interested candidates can apply by sending their updated resume to:
📧 Email: pradnya.raut@accutestglobal.com