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ICON

Clinical Trial Manager

France, Paris

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hirly's read of this role

Seniority
Lead / management
Country
FR
Work mode
On-site / unstated
First seen by hirly
27 Sept 2026

Derived automatically from the posting. Upload your resume above to see how the role scores against it.

the posting

Clinical Trial Manager At ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON’s global expertise.

As the world’s largest FSP organisation, with over 90 sponsor partnerships, we offer stability, career development and a collaborative environment where your work contributes to the development of treatments that benefit patients worldwide.

The COM role is equivalent Experienced Contract Specialists , who will be responsible for preparing and negotiating budget grids , drafting initial clinical trial agreements , and managing contract amendments (addenda) throughout the lifecycle of the study.

Their responsibilities will include:

  • Developing and reviewing site budget proposals in compliance with sponsor requirements and local regulations.
  • Drafting, negotiating, and finalizing initial agreements with investigational sites and other study vendors.
  • Preparing, reviewing, and executing contract amendments arising from protocol changes, budget revisions, study extensions, or operational updates.
  • Ensuring contractual documents are completed accurately and within agreed timelines.
  • Collaborating closely with Clinical Operations, Legal, Finance, and site personnel to facilitate efficient study start-up and ongoing trial conduct.
  • Maintaining contract documentation and ensuring compliance with applicable regulatory and company requirements.

Your Profile:

You will have solid clinical trial management experience, with the ability to manage competing priorities and develop your team.

Required qualifications and experience:

  • University degree in medicine, science, or equivalent combination of education & experience
  • Demonstrated ability to drive the clinical deliverables of a study
  • Subject matter expertise in the designated therapeutic area
  • Prior monitoring experience is preferred
  • Willingness to travel as required (approximately 25%)

Employment with ICON is contingent upon having the legal right to work in the country where the role is based.

Rewards & Benefits

ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.

Benefits may include:

  • Competitive base salary and performance related incentives
  • Health and wellbeing programmes including medical, dental, and vision coverage where applicable
  • Retirement and pension plans
  • Life assurance and disability coverage
  • Employee assistance programmes and wellbeing resources
  • Learning and development opportunities through structured training and career pathways

Benefits may vary depending on role and location.

Visit our careers site to read more about the benefits ICON offers.

Inclusion and Accessibility

ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.

If you require reasonable accommodations during the recruitment process, please let us know or submit a request here .

Are you a current ICON Employee? Please click here to apply

Original posting on ICON's site ↗

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