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ICON plc

Clinical Trial Liaison

Posted 4 days ago
$110K - $138K per year
2-5 years experience
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AI Summary

The Clinical Trial Liaison designs and implements clinical trial enrollment strategies while analyzing complex medical data to ensure regulatory compliance. They act as a primary point of contact between sponsors, investigators, and participants to optimize trial outcomes and patient retention.

Clinical Trial Liaison, Northeast

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.


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.

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

$110,520.00-$138,150.00

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

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