- Location
- Bengaluru, India
- Type
- Full-time
- Department
- Healthcare
- Experience
- 3+ years
- Source
- Keka
Description
Location: Bengaluru
Employment Type: Full-time
Experience: 3–5 years
Qualification: BDS / MDS
About the Role
We are seeking a Dentist to support and conduct oral and dental clinical studies at MS Clinical Research. The role will involve performing protocol-specific dental assessments, participant screening and evaluation, clinical documentation, and supporting the successful execution of oral health and dental research studies in compliance with study protocols, ICH-GCP, SOPs, and applicable regulatory requirements.
The ideal candidate should have strong clinical dental knowledge, good documentation skills, and an interest in clinical research.
Key Responsibilities
Oral & Dental Clinical Studies
- Conduct oral and dental examinations as per study protocols and approved procedures.
- Screen and assess participants for study eligibility based on inclusion and exclusion criteria.
- Perform protocol-specific dental assessments, oral examinations, and clinical evaluations.
- Obtain and document informed consent before conducting study-related procedures.
- Assess and document participants' oral health status and clinical findings accurately.
- Perform dental assessments required for oral care, dental products, oral hygiene products, and cosmetic/therapeutic oral studies.
- Monitor participants for adverse events (AEs) and report them appropriately as per the protocol and applicable requirements.
- Ensure participant safety throughout the study and escalate any clinically significant findings.
- Maintain accurate and complete source documents, CRFs/eCRFs, dental examination records, and other study-related documentation.
- Ensure all study procedures are conducted in accordance with the approved protocol, SOPs, ICH-GCP, and applicable regulatory requirements.
- Support investigators during study visits and participant assessments.
- Participate in sponsor meetings, monitoring visits, audits, and inspections as required.
- Coordinate with Clinical Operations, Clinical Research Coordinators, QA, Medical Writing, and Sponsors for smooth study execution.
- Review and provide clinical inputs on study-related dental and oral health documentation when required.
- Contribute to the identification and resolution of protocol deviations and documentation discrepancies.
- Maintain confidentiality and ensure proper handling of participant and study-related information.
Clinical Documentation
- Accurately document clinical findings, dental assessments, procedures, and participant observations.
- Review CRFs/eCRFs and source documents for completeness and consistency.
- Provide appropriate clinical inputs for study reports and other research documentation.
- Ensure timely completion of study-related documentation within defined timelines.
- Maintain proper documentation in accordance with ALCOA+ principles and GCP requirements.
Candidate Profile
- BDS or MDS from a recognized institution.
- 3–5 years of experience in dental clinical practice, clinical research, or oral/dental studies.
- Experience in conducting oral examinations and dental assessments.
- Good understanding of clinical trial methodology and ICH-GCP.
- Prior experience in clinical research or dental/oral product studies will be an added advantage.
- Strong clinical documentation and record-keeping skills.
- Good communication and interpersonal skills.
- Ability to work effectively with cross-functional clinical research teams.
- Detail-oriented, scientifically driven, and comfortable working in a research environment.
- Willingness to participate in participant-facing clinical study activities.
Key Competencies
- Dental & Oral Clinical Assessment
- Participant Screening & Evaluation
- Clinical Documentation
- Informed Consent Process
- ICH-GCP Compliance
- Clinical Trial Protocol Adherence
- Adverse Event Identification & Reporting
- Source Documentation
- Attention to Detail
- Communication & Team Collaboration
Why Join Us?
- Opportunity to work on oral and dental clinical research studies.
- Exposure to clinical research processes and GCP-compliant study conduct.
- Collaboration with multidisciplinary clinical research and scientific teams.
- Opportunity to contribute to research involving innovative oral healthcare and dental products.
Skills
GCPCompliance