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ICON

Clinical Trial Liaison

Poland, Warsaw

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hirly's read of this role

Seniority
Mid level
Country
PL
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

  • POL-HB-SCP
  • 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.

As a Clinical Trial Liaison at ICON, you will design and analyse clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies.

What You Will Do:

Your role will involve delivering clinical research work to a high standard, working closely with your team and stakeholders.

Key responsibilities include:

Collaborate with cross-functional teams to design and implement effective clinical trial enrollment strategies.

Analyze and interpret clinical trial data, ensuring accuracy and compliance with regulatory standards.

Foster strong relationships with study sites and investigators to enhance patient recruitment and retention.

Act as a liaison between sponsors, investigators, and study participants, providing support and guidance throughout the enrollment process.

Contribute to the continuous improvement of enrollment processes and strategies to optimize trial outcomes.

Your Profile:

You will bring relevant clinical research experience, along with the following qualifications and skills.

Required qualifications and experience:

Bachelor's degree in a relevant field, such as life sciences or healthcare.

Proven experience in clinical trial enrollment or related roles.

Strong analytical and problem-solving skills with the ability to interpret complex medical data.

Excellent communication and interpersonal skills to build and maintain effective relationships with stakeholders.

Detail-oriented with a commitment to ensuring accuracy and compliance in all aspects of clinical trial enrollment.

#LI-DD1

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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