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Clinical Research Manager (CRM) Lead

MSD


Job Location:

Paris - France

Monthly Salary: Not provided by the employer
Posted: 7 August 2026 (25 days ago)
Application Deadline: 4 November 2026
Vacancies: 1 Vacancy

Job Summary

Job Description

An amazing opportunity has arisen for a Clinical Research Manager (CRM) Lead.

We aspire to be the premier research-intensive biopharmaceutical company. Were at the forefront of research to deliver innovative health solutions that advance the prevention and treatment of diseases around the world.

Join us in our mission to use the power of leading-edge science to save and improve lives.

Responsibilities

  • Lead and oversee a portfolio of clinical trials across one or more Therapeutic Areas ensuring successful delivery from feasibility through study close-out.

  • Drive study performance by ensuring enrollment quality timelines milestones and compliance with ICH-GCP local regulations and our standards.

  • Develop and implement operational strategies quality plans and risk mitigation approaches to ensure optimal execution of the clinical trial portfolio.

  • Lead coach and develop a team of Clinical Research Managers fostering high performance talent development succession planning and employee engagement.

  • Build strong partnerships with internal cross-functional stakeholders and external collaborators including investigators sites vendors and regulatory authorities.

  • Contribute to country and global strategic initiatives supporting the growth of clinical research capabilities and the successful delivery of the development pipeline.

Skills & Experience

  • Extensive experience in clinical research operations including clinical trial management project leadership and team management.

  • Strong knowledge of ICH-GCP regulatory requirements clinical trial processes and the local clinical research environment.

  • Demonstrated leadership capabilities with experience developing motivating and managing high-performing teams.

  • Excellent project management organizational and problem-solving skills with the ability to prioritize multiple complex initiatives simultaneously.

  • Strong communication collaboration and stakeholder management skills in a global and cross-functional environment.

  • Strategic mindset with the ability to drive execution manage change influence stakeholders and build long-term partnerships.

Required Skills:

Clinical Research Management Clinical Sciences Clinical Study Design Decision Making Early Clinical Development Medical Research Oncology Trials People Leadership

Preferred Skills:

Current Employees apply HERE

Current Contingent Workers apply HERE

Search Firm Representatives Please Read Carefully
Merck & Co. Inc. Rahway NJ USA also known as Merck Sharp & Dohme LLC Rahway NJ USA does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place introductions are position specific. Please no phone calls or emails.

Employee Status:

Regular

Relocation:

VISA Sponsorship:

Travel Requirements:

Flexible Work Arrangements:

Hybrid

Shift:

Valid Driving License:

Hazardous Material(s):

Job Posting End Date:

08/19/2026

*A job posting is effective until 11:59:59PM on the day BEFOREthe listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.


Required Experience:

Manager


About Company

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Merck & Co., Inc., Kenilworth, New Jersey, USA is known as “Merck” in the United States, Canada & Puerto Rico. We are known as “MSD” in Europe, Middle East, Africa, Latin America & Asia Pacific. We are a global biopharmaceutical leader with a diverse portfolio of prescription medicine ... View more

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