Clinical Research Coordinator, Dental – Colgate-Palmolive

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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