Clinical Research Coordinator, Dental (Third-Party Payroll)

Colgate Palmolive; Maharashtra; On-site; INR 800,000 - 1,400,000; Full time

Job summary

Colgate-Palmolive in Mumbai, India is seeking a Dentist with 1–2 years post-degree experience to support clinical trial execution, site management, and regulatory compliance. You will participate in end-to-end study execution, recruit and screen participants, obtain informed consent, track safety, manage investigational products, and help prepare reports and documentation.

This role offers exposure to global R&D, opportunities in quality and safety, and collaboration with cross-functional teams

Qualifications

• Bachelor’s Degree in Dentistry (BDS) from a recognized institution.
• 1–2 years of post-degree experience in active clinical practice.
• Familiarity with IEC/IRB, GCP, and regulatory guidelines.
• Strong organizational, written and verbal communication skills.
• Willingness to travel up to 10%.

Responsibilities

• Study Execution: Participate in the end-to-end execution and daily management of internal and external clinical studies.
• Participant Recruitment & Screening: Identify, screen, and enroll eligible study participants according to protocol criteria.
• Informed Consent Process: Facilitate the informed consent process under PI supervision, ensuring participants are properly informed and documentation is accurately completed.
• Safety & Adverse Event Tracking: Monitor study subjects, record adverse events (AEs) or protocol deviations, and report them promptly.
• Investigational Product Handling: Manage clinical test products, including secure storage, accountability, and proper dispensation.
• Data Integrity, Quality Assurance & Scientific Reporting: Maintain data accuracy and integrity in data collection and management.
• Reporting & Dissemination: Assist in compiling clinical trial data and organizing study documentation for reports and presentations.
• Regulatory & GCP Compliance: Maintain TMF and coordinate submissions with IEC/IRB.

Skills

Clinical operations

GCP knowledge

Regulatory compliance

Study coordination

Data management

Education

Bachelor’s Degree in Dentistry (BDS)

Tools

EDC systems

IEC/IRB collaboration

Job description

No Relocation Assistance Offered

Job Number #176382 - Mumbai, Maharashtra, India

Who We Are

Colgate-Palmolive Company is a global consumer products company operating in over 200 countries specialising in Oral Care, Personal Care, Home Care, Skin Care, and Pet Nutrition. Our products are trusted in more households than any other brand in the world, making us a household name!

Key Responsibilities

• Study Execution, Clinical Operations & Subject Management
• Study Execution: Participate in the end-to-end execution and daily management of internal and external clinical studies.
• Participant Recruitment & Screening: Identify, screen, and enroll eligible study participants according to protocol criteria.
• Informed Consent Process: Facilitate the informed consent process under PI supervision, ensuring participants are properly informed and documentation is accurately completed.
• Safety & Adverse Event Tracking: Monitor study subjects, record adverse events (AEs) or protocol deviations, and report them promptly.
• Investigational Product Handling: Manage clinical test products, including secure storage, accountability, and proper dispensation.
• Data Integrity, Quality Assurance & Scientific Reporting
• Data Integrity & Quality Assurance: Maintain the highest standards of accuracy and integrity in data collection, electronic data entry (CRFs/EDC), and data management.
• Reporting & Dissemination: Assist in compiling clinical trial data, populating Case Report Forms (CRFs/EDC), and organizing study documentation for reports and presentations.
• Operations, Administration & Facility Maintenance
• Departmental Administrative Activities: Execute day-to-day administrative and financial operations for the unit, including raising, and tracking Purchase Order requests, verifying study invoices against payment milestones, and assisting with operational budget tracking. Facilitate the drafting, processing, and execution of Clinical Trial Agreements (CTAs), service contracts, and Non-Disclosure Agreements (NDAs) in close collaboration with internal teams. Serve as the primary liaison for third-party vendors and suppliers to ensure timely delivery of research services and clinical supplies.
• Facility & Equipment Maintenance: Ensure clinical facilities, testing equipment, and workspaces are properly calibrated, operational, and maintained per standard operating procedures (SOPs).
• Audit Readiness & Site Compliance: Maintain continuous site inspection and audit readiness in strict adherence to Quality & Safety standards, Good Clinical Practice (GCP), and corporate policies.
• Regulatory Compliance & Collaboration
• Regulatory & GCP Compliance: Maintain Trial Master Files (TMF) and coordinate submissions/approvals with Institutional Ethics Committees (IEC/IRB).
• Multidisciplinary Team Collaboration: Work collaboratively within a multidisciplinary team environment across cross-functional R&D and business units.

Candidate Profile & Requirements

Category

Qualifications & Competencies

Education

Bachelor’s Degree in Dentistry (BDS) from a recognized institution.

Clinical & Professional Experience

Minimum 1 to 2 years of post-degree experience in active clinical dental practice.

Research Background

Demonstrated interest in dental research; prior exposure to clinical trials, basic research, or academic research projects is a strong plus.

Regulatory & Quality

Knowledge of regulatory requirements, ethical guidelines (IEC/IRB), and GCP standards.

Admin & Facility Skills

High organizational ability to handle departmental administration, facility maintenance, and audit readiness.

Teamwork & Communication

Proven ability to work collaboratively in a multidisciplinary environment with excellent written, verbal, and presentation skills.

Operational Flexibility

Flexible working hours to meet trial demands; willing to travel up to 10%.

Computer Skills

Experience working with electronic data management systems and software suites.

What You Will Learn & Career Growth Opportunities

• Functional Linkages & Corporate R&D: Gain a complete view of corporate R&D and global technology integration.
• Operational Excellence: Build advanced capabilities in clinical trial execution, site management, and facility maintenance.
• Mentorship & Coaching: Receive structured coaching on technical rigor and soft skills.
• Quality & Safety Rigor: Master Colgate's premier Quality & Safety principles to ensure safe workplaces and audit-ready research environments.

Our Commitment to Inclusion

Our journey begins with our people—developing strong talent with diverse backgrounds and perspectives to best serve our consumers around the world and fostering an inclusive environment where everyone feels a true sense of belonging. We are dedicated to ensuring that each individual can be their authentic self, is treated with respect, and is empowered by leadership to contribute meaningfully to our business.

Equal Opportunity Employer

Colgate is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, colour, religion, gender, gender identity, sexual orientation, national origin, ethnicity, age, disability, marital status, veteran status (United States positions), or any other characteristic protected by law.

Reasonable accommodation during the application process is available for persons with disabilities. Please complete this request form should you require accommodation.

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