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  5. Clinical Trial Liaison
Investigative Reporters and Editors logo

Clinical Trial Liaison

Not Disclosed•Full-TimeRemote

location_on1769, San Jacinto Street, Downtown, Houston, Harris County, Texas, 77002, United States

Apply Now

About ICON

ICON plc is a world-leading healthcare intelligence and clinical research organization. We are proud to foster an inclusive environment that drives innovation and excellence. Our mission is to shape the future of clinical development by bringing together the best talent to solve complex challenges in healthcare.

About the Role

As a field-based Clinical Trial Liaison, you will serve as a highly trained site engagement specialist, bridging the gap between clinical strategy and on-the-ground execution. Your primary focus is to provide scientific and clinical support to investigators and site staff, ensuring a thorough understanding of study design and procedures to achieve clinical trial goals.

Beyond technical support, you will function as a recruitment specialist, developing and optimizing strategies at both the site and study levels to drive successful patient enrollment. This role thrives on active engagement, whether visiting study sites or attending industry meetings and conferences. You will be responsible for executing strategies that widen access for patients and translating best practices into local tactical actions.

The ideal candidate will collaborate cross-functionally with key stakeholders, including medical and scientific leaders, advocates, and decision-makers across the ecosystem. Success in this position requires a proactive approach to cultivating relationships and recruiting the most appropriate sites to participate in trials, all while navigating a landscape that requires up to 75% travel.

Hiring Process

If you are interested in this role but unsure if you meet all the requirements, we encourage you to apply regardless. There is a strong chance you are exactly what we are looking for, whether for this position or other opportunities within ICON.

Our Culture and Commitment

At ICON, inclusion and belonging are fundamental to our culture and values. We are dedicated to providing an inclusive and accessible environment for all candidates. Our success depends on the quality of our people, which is why we prioritize building a diverse culture that rewards high performance and nurtures talent.

ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or protected veteran status. If you require a reasonable accommodation for any part of the application process due to a medical condition or disability, please let us know or submit a request through our careers site.

Work location

Work model: Remote

location_on

1769, San Jacinto Street, Downtown, Houston, Harris County, Texas, 77002, United States

Houston, Texas

Key Responsibilities

  • check_circleProvide scientific and clinical support to investigators and site staff
  • check_circleCultivate relationships and recruit appropriate sites to participate in trials
  • check_circleEnsure study sites thoroughly understand study design and procedures
  • check_circleCollaborate cross-functionally with medical leaders and key decision makers
  • check_circleEngage on-site and at industry meetings to execute patient access strategies
  • check_circleTranslate best practices into local tactical actions for clinical trials
  • check_circleDevelop and optimize strategies to drive successful patient enrollment

Requirements

  • verifiedDoctoral degree (M.D., PharmD or PhD) required
  • verifiedExperience in clinical research environment in Pharma, Biotech, or CRO preferred
  • verifiedTherapeutic expertise in cardiometabolic, neuroscience, or oncology preferred
  • verifiedAbility to travel up to 75% nationally and internationally
  • verifiedBased within easy access to a major airport

Nice to Have

Experience in a clinical research environment in Pharma, Biotech, or CRO in scientific and/or clinical operations. Ideal therapeutic expertise in cardiometabolic, neuroscience or oncology.

Benefits & Perks

check_circleVarious annual leave entitlementscheck_circleA range of health insurance offerings for you and your familycheck_circleCompetitive retirement planning offerings to maximize savingscheck_circleGlobal Employee Assistance Programme via TELUS Health with 24-hour accessLife assurance coverage
Investigative Reporters and Editors logo
Company

Investigative Reporters and Editors

Industry

scientific & qa

View company profilearrow_forwardlanguageWebsite
Quick Overview

Experience

Mid Level

Education

Doctoral degree (M.D., PharmD, or PhD) required

Job Type

Full-Time

Skills Required

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Skills, education and keywords

Skills: Clinical Research, Clinical Operations, Clinical Development, Cardiometabolic, Neuroscience, Oncology.

Education: Doctoral degree (M.D., PharmD, or PhD) required.

Frequently asked questions about Clinical Trial Liaison at Investigative Reporters and Editors

What does a Clinical Trial Liaison at Investigative Reporters and Editors do?expand_more
In this Clinical Trial Liaison at Investigative Reporters and Editors role, you will provide scientific and clinical support to investigators and site staff; cultivate relationships and recruit appropriate sites to participate in trials; ensure study sites thoroughly understand study design and procedures; and collaborate cross-functionally with medical leaders and key decision makers.
What are the requirements for this Clinical Trial Liaison role?expand_more
To qualify for the Clinical Trial Liaison at Investigative Reporters and Editors position, applicants should have: Doctoral degree (M.D., PharmD or PhD) required; Experience in clinical research environment in Pharma, Biotech, or CRO preferred; Therapeutic expertise in cardiometabolic, neuroscience, or oncology preferred; Ability to travel up to 75% nationally and internationally; and Based within easy access to a major airport.
Where is the Clinical Trial Liaison role at Investigative Reporters and Editors located?expand_more
Clinical Trial Liaison at Investigative Reporters and Editors is based in 1769, San Jacinto Street, Downtown, Houston, Harris County, Texas, 77002, United States. This is a remote role.
Is this Clinical Trial Liaison job remote, hybrid, or on-site?expand_more
Investigative Reporters and Editors has listed this Clinical Trial Liaison role as remote.
How much experience is required for this Clinical Trial Liaison role?expand_more
Candidates for Clinical Trial Liaison at Investigative Reporters and Editors should have mid level.
What skills do you need for the Clinical Trial Liaison role at Investigative Reporters and Editors?expand_more
Key skills for Clinical Trial Liaison at Investigative Reporters and Editors include Clinical Research; Clinical Operations; Clinical Development; Cardiometabolic; Neuroscience; and Oncology.
What education is required for Clinical Trial Liaison at Investigative Reporters and Editors?expand_more
Educational requirements for this role: Doctoral degree (M.D., PharmD, or PhD) required.
What category does the Clinical Trial Liaison role belong to?expand_more
Clinical Trial Liaison at Investigative Reporters and Editors is part of the scientific & qa job category on Recrutus.
Recrutus

Curating the world's most innovative career opportunities. We bridge the gap between visionary talent and industry-leading companies.

Search roles by city, category, skill, or job type — explore verified US employers, salary benchmarks, and remote-friendly teams hiring nationwide.

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Recrutus helps candidates discover roles that match their skills and helps teams reach qualified applicants faster. Browse by metro, discipline, or work style — from internships to senior leadership.

© 2026 Recrutus. All rights reserved.
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check_circle
check_circleFlexible country-specific optional benefits including childcare vouchers
check_circleBike purchase schemes
check_circleDiscounted gym memberships
check_circleSubsidised travel passes
check_circleHealth assessments
Clinical ResearchClinical OperationsClinical DevelopmentCardiometabolicNeuroscienceOncology
US privacy notice
Accessibility