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ICON

Senior Clinical Trial Manager - Biotech

Romania, Bucharest · Spain, Madrid · Bulgaria, Sofia · Portugal, Lisbon · Poland, Warsaw · South Africa, Johannesburg · Ireland, Dublin · Hungary, Budapest · UK, Reading · Latvia, Riga · Lithuania, Vilnius · Poland, Gdansk · Czech Republic, Prague

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hirly's read of this role

Seniority
Lead / management
Countries
RO, ES, BG, PT, PL, ZA, IE, HU, GB, LV, LT, CZ
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
  • ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.

As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.

We are currently seeking a Clinical Trial Manager to join our diverse and dynamic team at ICON Plc - this position will sit within ICON Biotech. In this critical role, you will be responsible for overseeing the planning, execution, and successful completion of clinical trials, ensuring adherence to timelines, budgets, and regulatory guidelines. As a leader in our research department, you will collaborate with cross-functional teams, manage site relationships, and provide strategic guidance to drive the successful delivery of clinical trial outcomes.

What you will be doing

Plan and manage all aspects of clinical trials, ensuring adherence to timelines, budget, and quality standards.

Collaborate with cross-functional teams to establish and implement clinical trial protocols and procedures.

Build and manage strong relationships with trial investigators and stakeholders.

Ensure all trials are conducted in compliance with local, national, and international regulations and ethical guidelines.

Problem-solve and make critical decisions regarding trial design, vendor selection, and risk management.

Your Profile

  • University degree in medicine, science, or equivalent combination of education & experience
  • Multi country Clinical Trial Management expertise

Demonstrated ability to drive the clinical deliverables of a study

Subject matter expertise in the designated therapeutic area

Prior monitoring experience is preferred

Ability to travel up to 20%

#LI-JD1

#LI-Remote

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 .

Salary Range

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

Original posting on ICON's site ↗

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