Clinical Research Coordinator, Dental – Colgate-Palmolive
Colgate-Palmolive is hiring a Clinical Research Coordinator, Dental (Third-Party Payroll) for its R&D operations in Mumbai, Maharashtra.
The role is focused on coordinating oral care clinical trials, participant management, clinical data integrity, regulatory compliance and audit readiness.
Candidates with a BDS degree and 1–2 years of active clinical dental practice are eligible for this opportunity.
The position offers exposure to clinical research, global R&D collaboration, Good Clinical Practice (GCP), clinical trial methodologies and cross-functional operations.
Colgate-Palmolive Clinical Research Coordinator – Dental
Job Details
- Company: Colgate-Palmolive Company
- Position: Clinical Research Coordinator, Dental (Third-Party Payroll)
- Job Number: 176382
- Department: Research & Development
- Location: Mumbai, Maharashtra, India
- Work Mode: On-site
- Employment Type: Full Time
- Payroll: Third-Party Payroll
- Travel: Up to 10%
- Posting Start Date: 27 September 2026
- Relocation Assistance: Not offered
Clinical Research Coordinator – Study Execution & Clinical Operations
The Clinical Research Coordinator will support the end-to-end execution and daily management of internal and external clinical studies related to oral care.
Participant Recruitment & Screening
- Identify, screen and enroll eligible study participants according to protocol criteria.
- Facilitate the informed consent process under Principal Investigator supervision.
- Ensure participants are properly informed and documentation is accurately completed.
- Monitor study subjects and record adverse events (AEs) or protocol deviations.
- Report safety events and protocol deviations promptly.
Investigational Product Handling
- Manage clinical test products.
- Ensure secure storage and accountability of clinical test products.
- Support proper dispensation of investigational or clinical test products.
Data Integrity & Quality Assurance
Clinical Data Management
- Maintain accuracy and integrity of clinical trial data.
- Perform electronic data entry using CRFs/EDC.
- Support clinical data management activities.
- Assist in compiling clinical trial data and organizing study documentation.
Scientific Reporting
- Support preparation of clinical trial reports and presentations.
- Populate Case Report Forms (CRFs/EDC).
- Maintain study-related documentation according to applicable requirements.
Operations & Administrative Responsibilities
Departmental Administration
The Clinical Research Coordinator will support day-to-day administrative and financial operations, including:
- Raising and tracking Purchase Order requests.
- Verifying study invoices against payment milestones.
- Supporting operational budget tracking.
- Assisting with Clinical Trial Agreements (CTAs).
- Supporting processing and execution of service contracts and Non-Disclosure Agreements (NDAs).
- Coordinating with internal teams for study-related agreements and documentation.
Vendor & Supplier Coordination
- Serve as a primary liaison for third-party vendors and suppliers.
- Coordinate timely delivery of research services and clinical supplies.
- Support vendor-related activities associated with clinical research operations.
Facility Maintenance & Audit Readiness
Facility and Equipment Management
- Ensure clinical facilities and testing equipment remain operational.
- Ensure workspaces are properly maintained.
- Support calibration and maintenance of testing equipment according to SOPs.
Audit & Site Compliance
- Maintain continuous inspection and audit readiness.
- Follow Quality & Safety standards.
- Ensure compliance with Good Clinical Practice (GCP) and corporate policies.
Regulatory Compliance & Clinical Research
Regulatory and GCP Activities
- Maintain Trial Master Files (TMF).
- Coordinate submissions and approvals with Institutional Ethics Committees (IEC/IRB).
- Follow applicable regulatory and ethical requirements.
- Support compliance throughout the clinical trial lifecycle.
Cross-Functional Collaboration
- Work within a multidisciplinary team.
- Collaborate with cross-functional R&D and business units.
- Coordinate effectively with internal teams, external vendors and other stakeholders.
Eligibility & Qualifications
Educational Qualification
- Bachelor’s Degree in Dentistry (BDS) from a recognized institution.
Clinical Experience
- 1–2 years of post-degree experience in active clinical dental practice.
Research Background
Prior exposure to any of the following is a strong advantage:
- Dental research
- Clinical trials
- Basic research
- Academic research projects
Regulatory & Quality Knowledge
Candidates should have knowledge of:
- Regulatory requirements
- Ethical guidelines
- IEC/IRB requirements
- Good Clinical Practice (GCP) standards
Skills & Competencies
- Strong organizational skills
- Clinical research coordination
- Excellent written and verbal communication
- Presentation skills
- Ability to work in a multidisciplinary environment
- Ability to manage departmental administration
- Facility maintenance and audit-readiness activities
- Attention to detail
- Ability to work with electronic data management systems
- Familiarity with relevant software suites
- Flexibility to meet clinical trial requirements
- Willingness to travel up to 10%
Eligible Qualification Courses
BDS | Bachelor of Dental Surgery
Career Growth & Learning Opportunities
The role provides exposure to:
- Corporate R&D and global technology integration
- Clinical trial execution
- Clinical research operations
- Site management
- Facility maintenance
- Clinical data integrity
- Quality and Safety systems
- Audit-ready research environments
- Global R&D collaboration
- Technical and professional mentorship
Location & Work Environment
Job Location: Mumbai, Maharashtra, India
Work Mode: On-site
Travel Requirement: Up to 10% of working time.
The position requires flexibility in working hours according to clinical trial requirements.
How to Apply
Interested and eligible candidates can apply through the official Colgate-Palmolive careers portal:
Apply for Clinical Research Coordinator, Dental – Colgate-Palmolive
Job Number: 176382
Job Summary
| Category | Details |
|---|---|
| Company | Colgate-Palmolive Company |
| Vacancies | Clinical Research Coordinator, Dental (Third-Party Payroll) |
| Required Education | BDS, Bachelor’s Degree in Dentistry |
| Experience | 1–2 years of post-degree experience in active clinical dental practice |