Medical Writer (Protocol Writer) Accutest Research
- Accutest Hiring Medical Writer (Protocol Writer) | B.Pharm & B.Sc Apply Now
- Company Overview
- Job Role & Responsibilities
- Eligibility / Qualifications
- Educational Qualification:
- Experience:
- Skills Required:
- Location & Salary
- Application Process
- Frequently Asked Questions (FAQs)
- Is this role suitable for freshers?
- What does a protocol writer do?
- What skills are essential for this role?
- Is experience in CRO mandatory?
- What is the work location?
Accutest Hiring Medical Writer (Protocol Writer) | B.Pharm & B.Sc Apply Now
Looking to build a career in medical writing and clinical research? Accutest Research Laboratories (India) Pvt. Ltd. is hiring for the position of Medical Writer – Protocol Writer in the Clinical Pharmacology Unit at Navi Mumbai. This is an excellent opportunity for candidates with 2–4 years of experience in clinical research, regulatory writing, and protocol development to work with a reputed CRO.
With the increasing demand for clinical trials, regulatory documentation, and pharmaceutical research, medical writing roles are becoming one of the most in-demand and high-growth career paths in the pharma and CRO industry.
Company Overview
Accutest Research Laboratories (I) Pvt. Ltd. is a well-established Contract Research Organization (CRO) known for delivering high-quality clinical research, bioequivalence studies, and regulatory support services. The company plays a key role in accelerating drug development and ensuring compliance with global regulatory standards.
Working at Accutest offers exposure to clinical trial protocols, regulatory submissions, and scientific documentation aligned with global guidelines such as ICH-GCP, making it an ideal workplace for professionals aiming to grow in medical writing and regulatory affairs.
Job Role & Responsibilities
As a Medical Writer (Protocol Writer), you will be responsible for preparing, reviewing, and managing clinical trial protocols and regulatory documents.
Key responsibilities include:
- Develop and write clinical trial protocols in compliance with regulatory guidelines
- Collaborate with cross-functional teams including clinical operations and regulatory affairs
- Ensure accuracy, clarity, and scientific integrity in documentation
- Review and edit protocol documents for consistency and compliance
- Support preparation of regulatory submission documents
- Maintain documentation standards as per ICH-GCP and SOPs
- Assist in updating and maintaining protocol templates and writing standards
This role directly contributes to the safe and efficient execution of clinical trials and supports global drug development processes.
Eligibility / Qualifications
Candidates must meet the following criteria:
Educational Qualification:
B.Pharm, B.Sc Life Sciences, Biotechnology, Microbiology, Biochemistry
Experience:
- 2 to 4 years of experience in medical writing or clinical research
Skills Required:
- Strong understanding of clinical trial protocols and regulatory guidelines
- Good knowledge of ICH-GCP standards
- Excellent scientific writing and documentation skills
- Attention to detail and analytical thinking
- Strong communication and coordination skills
Location & Salary
- Location: Koperkhairane, Navi Mumbai
- Salary: Not disclosed (competitive as per industry standards)
- Preference: Immediate joiners preferred
Application Process
Interested candidates can apply by sending their updated resume:
Email: pradnya.raut@accutestglobal.com
Ensure your resume highlights relevant experience in medical writing, protocol development, or clinical research documentation.
Frequently Asked Questions (FAQs)
Is this role suitable for freshers?
No, this role requires 2–4 years of relevant experience in medical writing or clinical research.
What does a protocol writer do?
A protocol writer develops detailed clinical trial plans that guide how a study is conducted.
What skills are essential for this role?
Strong writing skills, knowledge of regulatory guidelines, and attention to detail are critical.
Is experience in CRO mandatory?
Experience in CRO or clinical research is highly preferred.
What is the work location?
The job is based in Navi Mumbai.
| Category | Details |
|---|---|
| Company | Accutest Research Laboratories |
| Vacancies | Medical Writer (Protocol Writer) |
| Required Education | B.Pharm, B.Sc Life Sciences, Biotechnology, Microbiology, Biochemistry |
| Experience | 2–4 Years |
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