Welcome Back

Google icon Sign in with Google
OR
I agree to abide by Pharmadaily Terms of Service and its Privacy Policy

Create Account

Google icon Sign up with Google
OR
By signing up, you agree to our Terms of Service and Privacy Policy
Instagram
youtube
Facebook

Clinical Research Associate, Dental

Colgate-Palmolive Company
0-2 years
Not Disclosed
Mumbai, Navi Mumbai, India
10 May 20, 2026
Job Description
Job Type: Full Time Hybrid Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, mRS and EQ-5D-5L., Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Job Overview

Job Title: Clinical Research Associate, Dental
Company: Colgate-Palmolive
Job Number: #173173
Location: Mumbai
Work Mode: On-site
Travel Requirement: Up to 10%
Relocation Assistance: Offered within country
Posting Start Date: 06/05/2026


About the Company

Colgate-Palmolive is a global consumer products company operating in more than 200 countries across:

  • Oral Care

  • Personal Care

  • Home Care

  • Skin Care

  • Pet Nutrition

The company focuses on innovation, inclusion, sustainability, and creating healthier futures for people and pets.


Role Summary

The Clinical Research Associate, Dental will join the Global Technology Center (GTC) in Mumbai under the Dental-Dermal Health Unit. The role involves managing in-house and external dental clinical studies while ensuring compliance with Good Clinical Practice (GCP), ethical standards, and regulatory requirements.


Key Responsibilities

1. Clinical Coordination & Management

  • Manage daily operations of the in-house dental clinic

  • Support execution of external oral health clinical studies

  • Coordinate study activities and timelines

2. Protocol Development & Documentation

  • Draft research protocols and study-related documentation

  • Ensure compliance with ethical principles and regulatory guidelines

  • Submit protocols for ethics committee approvals

3. Regulatory & Safety Compliance

  • Maintain infection control and hygiene standards

  • Ensure adherence to GCP requirements

  • Monitor participant safety and reporting procedures

4. Study Oversight

  • Supervise scheduling and protocol adherence

  • Monitor data quality and study progress

  • Identify issues and implement corrective actions

5. Governance & Regulatory Interaction

  • Act as primary contact for ethics committees and regulatory bodies

  • Handle adverse event reporting and facility-related inquiries

6. Financial Coordination

  • Assist with department budgeting and expense approvals

  • Coordinate with Clinical Manager on financial matters

7. Staff Training & Leadership

  • Train and supervise clinical support staff

  • Provide training to external site teams

  • Work effectively with cross-functional teams

8. Data Management & Reporting

  • Conduct data management and analysis

  • Prepare:

    • Interim reports

    • Final clinical study reports

    • Manuscripts

    • Scientific presentations


Required Qualifications

Educational Background

  • BDS or MDS degree in Dentistry

  • Licensed and qualified to conduct dental procedures and evaluations

Professional Experience

  • Experience in oral health clinical trials

  • Protocol writing and study execution expertise

  • Knowledge of GCP and clinical site documentation

Preferred Experience

  • Clinical facility administration and management

Skills Required

  • Strong written and verbal communication

  • Leadership and supervisory skills

  • Planning and prioritization abilities

  • Team collaboration skills


Work Environment & Culture

Core Values

  • Caring

  • Inclusive

  • Courageous

Inclusion Commitment

The company promotes diversity, equal opportunity, and an inclusive work environment where employees are encouraged to contribute authentically and meaningfully.