Clinical Research Manager (Dentist/Hygienist) (Therwil, BL, CH)

No Relocation Assistance Offered Job Number #175262 - Therwil, Switzerland, Switzerland

Who We Are

Colgate-Palmolive Company is a global consumer products company operating in over 200 countries specializing 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.

Clinical Research Manager (Dentist/Hygienist)

Job Details

• Position: Clinical Research Manager - Permanent (No relocation assistance).

• Expected Gross Annual Salary Range: 130,000 CHF - 153,000 CHF per year, determined on the basis of objective, transparent, and gender-neutral criteria.

• Variable Compensation: Eligibility to participate in bonus and incentive programs linked to company and/or individual performance.

Pay Transparency Notice

Initial compensation and benefits are determined in accordance with strict principles of equal pay, transparency, and non-discrimination. Detailed information regarding compensation, benefits, applicable employment terms and job classification will be provided during the recruitment process. In compliance with applicable legislation, candidates will not be asked to disclose their current or previous remuneration, nor will such information be sought during the recruitment process.

About the Post

Based at the Colgate-Palmolive facility in Therwil, Switzerland, this role focuses on conducting clinical studies and providing comprehensive support for clinical trials executed by the Dental Health Unit. We are seeking a highly motivated, capable individual with experience in applied health research.

The postholder will collaborate with team members to coordinate and undertake research studies aimed at improving global oral health, advancing oral care through novel methodologies, and translating knowledge into clinical care and best practices.

Core Responsibilities

• End-to-End Study Management: Manage the entire clinical research process, from protocol composition and study design to administration, execution, and analysis of oral care products, novel diagnostic devices, and interventions.

• Data & Analysis: Independently build relevant research databases and perform statistical analyses using statistical packages.

• Clinical Trial Execution: Serve as a clinical examiner in studies and perform trials in collaboration with other global Colgate-Palmolive Technology Centers.

• Compliance & Documentation: Maintain Trial Master Files (TMF) and clinical trial documentation in strict compliance with Good Clinical Practice (GCP) and local/national/company policies.

• Cross-Functional Collaboration: Partner with external research groups and internal business functions to identify collaborative links to dental diagnostic methods and support corporate research priorities.

• Reporting & Dissemination: Manage the drafting, writing, and reviewing of study reports and manuscripts for peer-reviewed publication.

• Site Supervision: Contribute to the training, onboarding, and supervision of clinical trial site staff.

Operational Requirements

• Flexibility: A flexible approach to working hours is essential to support the dynamic nature of clinical trials.

• Travel: Willingness and capability to travel to and operate at remote clinical sites for extended periods.

• Confidentiality: Strict adherence to confidentiality protocols regarding research data sponsored by commercial or pharmaceutical entities.

Required Qualifications

• A recognized Dental Degree (DDS / BDS) or a BSc in Dental Hygiene & Therapy (or equivalent recognized credential).

• Minimum 6 years of demonstrable clinical research experience.

• Track record of drafting clinical trial protocols and ethics forms.

• Experience managing CROs and protocol compliance.

• Strong organizational and prioritization skills.

• Accredited training in Good Clinical Practice (GCP).

• Excellent communication skills.

Preferred Qualifications

• Specific certifications relevant to clinical research operations.

• History of publishing peer-reviewed papers.

• Experience running clinical trials for Medical Devices.

• Proficiency in statistical analysis packages.

• Proficiency in a second language.

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, color, 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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