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 cutting-edge healthcare solutions.
- About the Role
- Key Responsibilities

Medical Writing- Prepare and review clinical and regulatory documents, including Protocols, CSRs, IBs, ICFs, CRFs/eCRFs, CERs, and regulatory submissions.
- Interpret clinical trial data and scientific literature to develop accurate medical and dental content.
- Ensure documents comply with ICH-GCP and applicable regulatory guidelines.
- Collaborate with cross-functional teams to deliver high-quality documentation.

Clinical Research (Dental)- Serve as a Principal Investigator (PI) or Sub-Investigator (Sub-I) for assigned studies.




- Screen and assess participants for eligibility and conduct protocol-specific dental examinations.
- Obtain and document Informed Consent before study procedures.
- Monitor participant safety and report AEs/SAEs as required.
- Maintain accurate source documents, CRFs/eCRFs, and study records.
- Ensure compliance with study protocols, ICH-GCP, SOPs, and regulatory requirements.
- Participate in sponsor visits, audits, and collaborate with Clinical Operations, CRCs, QA, and Sponsors.

Qualifications- BDS (MDS preferred).
- 2-5 years of experience in clinical research, medical writing, or dental clinical practice.
- Experience in preparing scientific and regulatory documents is preferred.
- Good understanding of ICH-GCP, clinical trial methodology, and regulatory requirements.
- Excellent scientific writing, communication, and documentation skills.
- Ability to manage both clinical research activities and medical writing deliverables.

📌 Dentist (Bengaluru)
🏢 MS Clinical
📍 Bengaluru