Location: Bangalore
Job Type: Full-time
Experience: 2–5 Years
About Us
MS Clinical Research Pvt. Ltd. (MSCR) is a leading Clinical Research Organization (CRO) specializing in clinical trials across dermatology, dentistry, medical devices, pharmaceuticals, cosmetics, and consumer healthcare. We are committed to delivering high-quality clinical research and scientific documentation that supports innovative healthcare solutions.
About the Role
We are seeking a detail-oriented and scientifically driven Medical Writer to develop high-quality clinical and regulatory documents supporting medical and dental research studies. The ideal candidate should possess strong scientific writing skills, an understanding of clinical research, and the ability to collaborate effectively with cross-functional teams to deliver accurate and compliant documentation.
Key Responsibilities
Medical Writing
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Prepare and review clinical and regulatory documents, including Protocols, CSRs, IBs, ICFs, CRFs/eCRFs, CERs, and regulatory submissions.
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Interpret clinical trial data and scientific literature to develop accurate medical and dental content.
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Ensure documents comply with ICH-GCP and applicable regulatory guidelines.
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Collaborate with cross-functional teams to deliver high-quality documentation.
Clinical Research (Dental)
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Serve as a Principal Investigator (PI) or Sub-Investigator (Sub-I) for assigned studies.
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Screen and assess participants for eligibility and conduct protocol-specific dental examinations.
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Obtain and document Informed Consent before study procedures.
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Monitor participant safety and report AEs/SAEs as required.
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Maintain accurate source documents, CRFs/eCRFs, and study records.
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Ensure compliance with study protocols, ICH-GCP, SOPs, and regulatory requirements.
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Participate in sponsor visits, audits, and collaborate with Clinical Operations, CRCs, QA, and Sponsors.
Qualifications
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BDS (MDS preferred).
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2–5 years of experience in clinical research, medical writing, or dental clinical practice.
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Experience in preparing scientific and regulatory documents is preferred.
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Good understanding of ICH-GCP, clinical trial methodology, and regulatory requirements.
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Excellent scientific writing, communication, and documentation skills.
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Ability to manage both clinical research activities and medical writing deliverables.
