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Icon Clinical Trial Jobs (NOW HIRING)

410 ICR United States USA

$110K - $138K/yr

Clinical Trial Liaison - Mid- Atlantic 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 ...

ICON

Senior Manager Clinical Trial Lead

Blue Bell, PA · On-site

Senior Clinical Trial Lead 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 ...

ICON

Team Lead, Site Operations (Oncology)

Lisle, IL · On-site

$68K - $85K/yr

This role is with Accellacare, part of ICON's clinical research network, where you'll play a key role in transforming the clinical trial experience for patients and sponsors alike. Our global site ...

ICON

Senior Clinical Research Associate

Blue Bell, PA · On-site

As a Senior CRA at ICON Plc, you will oversee and manage clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards. What You Will ...

Icon plc

Sr. Clinical Trial Manager

Blue Bell, PA · On-site

Senior Local Operations Manager - Oncology Solid Tumor - Home Based (US) ICON is a global health ... This may require development of local trial specific procedures and tools, recruitment planning ...

Icon plc

Team Lead, Site Operations (Oncology)

Lisle, IL · On-site

$68K - $85K/yr

This role is with Accellacare, part of ICON's clinical research network, where you'll play a key role in transforming the clinical trial experience for patients and sponsors alike. Our global site ...

ICON

Patient Recruitment Associate I

Winston Salem, NC · On-site

This role is with Accellacare, part of ICON's clinical research network, where you'll play a key role in transforming the clinical trial experience for patients and sponsors alike. Our global site ...

ICON

Patient Recruitment Associate I

Statesville, NC · On-site

This role is with Accellacare, part of ICON's clinical research network, where you'll play a key role in transforming the clinical trial experience for patients and sponsors alike. Our global site ...

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How much do icon clinical trial jobs pay per hour?

As of Aug 7, 2026, the average hourly pay for icon clinical trial in the United States is $37.67, according to ZipRecruiter salary data. Most workers in this role earn between $25.72 and $48.08 per hour, depending on experience, location, and employer.

What are the typical career advancement opportunities for individuals working in Icon Clinical Trial roles?

Professionals working in ICON Clinical Trial Associate roles often have clear pathways for career advancement within clinical research. Starting as an associate or coordinator, many progress to roles such as Clinical Research Associate (CRA), Project Manager, or Clinical Trial Manager, with increasing responsibilities in oversight and leadership. ICON supports professional development through mentorship, on-the-job training, and access to industry certifications, helping employees build expertise in regulatory standards and project management. This structure allows motivated individuals to gain diverse experience and move into higher-level positions, either within ICON or across the broader clinical research industry.

What are the key skills and qualifications needed to thrive in the Icon Clinical Trial position, and why are they important?

To thrive in an ICON Clinical Trial Associate or related role, you need a strong background in life sciences or a health-related field, familiarity with Good Clinical Practice (GCP), and strong organizational skills. Experience with clinical trial management systems (CTMS), electronic data capture (EDC) platforms, and relevant certifications such as SOCRA or ACRP are typically valuable. Attention to detail, effective communication, and the ability to work both independently and in teams are crucial soft skills. These competencies ensure the accurate and ethical conduct of clinical trials, facilitate regulatory compliance, and contribute to successful project outcomes.

What is an Icon Clinical Trial?

An ICON Clinical Trial job involves working for ICON plc, a global contract research organization (CRO) that provides outsourced development and commercialization services to pharmaceutical, biotechnology, and medical device companies. Employees in these roles support clinical research trials by managing study protocols, ensuring regulatory compliance, collecting and analyzing data, and coordinating with sponsors and healthcare professionals. Positions may range from clinical research associates (CRAs) and data managers to project managers and regulatory specialists. These roles require attention to detail, strong organizational skills, and knowledge of clinical trial processes and guidelines.

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What are the most commonly searched types of Icon Clinical Trial jobs? The most popular types of Icon Clinical Trial jobs are:
What states have the most Icon Clinical Trial jobs? States with the most job openings for Icon Clinical Trial jobs include:
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Icon Clinical Trial jobs near you
Infographic showing various Icon Clinical Trial job openings in the United States as of August 2026, with employment types broken down into 3% As Needed, 71% Full Time, 18% Part Time, and 8% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $78,347 per year, or $37.7 per hour.

Clinical Trial Liaison

410 ICR United States USA

On-site

$110K - $138K/yr

Full-time

Posted 17 days ago

Job description

Clinical Trial Liaison - Mid- Atlantic

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 analyze clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies.

What you will do:

Clinical Investigator Management 

  • Accountable for the full spectrum of investigator engagement from identification and qualification through enrollment, and support database lock, and study closeout 

  • Serve as a clinical trial scientific ambassador, ensuring investigators deeply understand protocol intent, scientific rationale, and patient eligibility requirements 

  • Develop and sustain strategic, high-trust relationships with investigators that span trials and therapeutic areas 

  • Influence enrollment by co-creating tailored recruitment strategies aligned with site capabilities, patient population realities, and study objectives 

  • Proactively find opportunities to reach new patients, accelerate enrollment and increase impact at priority sites, including for example, novel site models, community-based research initiatives etc 

  • Capture and elevate critical insights from sites to optimize feasibility, protocol design, and study conduct 

Clinical Trial Management 

  • Lead site-level strategy and risk planning to ensure strong and predictable enrollment and data delivery 

  • Leverage performance metrics to anticipate issues, intervene decisively, and maintain momentum toward clinical milestones 

  • Drive inspection readiness as a continuous discipline across sites 

  • Collaborate across functions and with vendor partners to resolve operational barriers, ensuring delivery with speed and quality 

  • Maintain advanced understanding of local treatment paradigms and standard of care to influence strategic country/site selection and protocol localization 

  • Provide oversight and quality assurance for vendor monitoring, escalating risks proactively 

  • Where applicable, lead end-to-end management of Post-Marketing Safety Studies in compliance with local regulations 

  • Business Management and Engagement 

  • Cultivate a portfolio of strategically aligned, high-impact investigators who consistently prioritize client trials 

  • Enable an exceptional investigator experience by being a responsive, knowledgeable, and valued scientific partner 

  • Collaborate cross-functionally (e.g., Medical, Clinical, Study Delivery) to align on trial and site priorities, troubleshooting challenges with urgency and creativity 

  • Conduct data-informed site prospecting and prioritization, contributing to trial competitiveness and regional strategic execution 

  • Maintain scientific fluency and therapeutic expertise to lead meaningful, solutions-focused discussions with site personnel 

  • Act as a key liaison between field teams, vendors, and investigators, ensuring alignment, shared purpose, and continuous knowledge transfer 

  • Partner closely with field team colleagues to elevate the investigator and site experience, ensuring seamless collaboration and improving enrollment outcomes and Investigator relationships 


You are:

  • Bachelor’s degree or equivalent; strong preference for scientific, clinical, or health-related fields 

  • Minimum 5 years of experience in clinical research or pharmaceutical industry with experience directly interacting with or working with HCPs and clinical sites  

  • Open to up to 60-80% travel during peak times (travel will vary)

  • Oncology experience required (Breast/Gyn experience preferred)

  • Location: Mid-Atlantic, Southeast Region


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