Clinical research associate india Jobs

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Clinical Research Associate, Dental

Colgate-Palmolive -
Mumbai, Maharashtra

Apply Now

Job details

Qualifications

Clinical research
Supervising experience
Clinical trials
Communication skills

Full job description

Relocation Assistance Offered Within Country
Job Number #173173 - 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!

Join Colgate-Palmolive, a caring, innovative growth company reimagining a healthier future for people, their pets, and our planet. Guided by our core values—Caring, Inclusive, and Courageous—we foster a culture that inspires our people to achieve common goals. Together, let's build a brighter, healthier future for all.

Brief Introduction

We are seeking a qualified dental professional to join our Global Technology Center (GTC) in Mumbai, India to join our Dental-Dermal Health Unit. The candidate will play a critical role in managing in house and external dental clinical studies, adhering to good clinical practice guidelines which encompass drafting and submitting protocols for ethics committee approval, training clinical staff and sites, ensuring participant safety, maintaining proper documentation and reporting procedures involving adverse events, and maintaining strict adherence to regulatory standards.

Key Responsibilities

Clinical Coordination & Management: Manage day-to-day operations of the in-house dental clinic. Help support the execution of external oral health clinical research studies.
Protocol & Documentation: Develop research protocols and other study documentation ensuring compliance to ethical principles and regulatory guidelines.
Regulatory & Safety Compliance: Oversee stringent infection control procedures, health and hygiene practices, and adherence to Good Clinical Practice (GCP) requirements and safety and quality standards.
Study Oversight: Manage clinical coordination, including scheduling, protocol adherence, data quality oversight (i.e. integrity of data collection), and reporting. Monitor study progress, identify potential issues, and implement corrective actions as needed to keep research on track.
Governance: Act as the primary on-site contact for ethics committees and regulatory bodies, particularly regarding Adverse Events or facility inquiries.
Financial Oversight: Coordinate approval of expenses and department budget with Clinical Manager.
Staff Leadership: Train and supervise in house clinical support staff and be available to train external site teams.
Data: Management and analysis.
Clinical study reports: Prepare interim and final reports, manuscripts, and presentations to disseminate research findings to the scientific community and other stakeholders.

Required Qualifications & Experience

Professional Credentials: Must be a trained dentist (BDS or MDS) with the appropriate credentials to conduct dental evaluations and procedures.
Clinical Research Expertise: Demonstrated experience in writing and executing protocols and conducting oral health clinical trials.
GCP Knowledge: Familiarity with Good Clinical Practice (GCP) requirements and site documentation.
Facility Management: Experience in administration and managing clinical facilities is preferred.
Communication: Good oral and written communication skills
Leadership: Demonstrated ability to work effectively in cross functional teams. Demonstrated ability to plan and prioritize tasks and have some supervisory experience.

#CPIL
#LI-AP1

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.

#LI-On-site

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Refine Your Search

Clinical Research Associate, Dental

Clinical Research Associate - II

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Research Associate—Medical Writing

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Senior Clinical Research Associate

Trainee Research Associate (C)

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Sr. Prosthetics and orthotics & Associate Manager for Mobility India (Assam)

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Sr. Research Associate

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