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Icon Clinical Research Jobs (NOW HIRING)

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 ...

Dentist ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to ...

Clinical Research Nurse - ICON San Antonio TX- PRN M-F Day Shift ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments ...

Team Lead, Site Operations - Hickory, NC (Onsite) ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients ...

Clinical Research Nurse - ICON San Antonio TX- PRN M-F Day Shift ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments ...

Senior CRA 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 ...

Clinical Research Nurse - ICON San Antonio TX- PRN M-F Day Shift ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments ...

Clinical Research Nurse 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 ...

Contract Senior Clinical Research Associate - Home-Based (US) ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to ...

Team Lead, Site Operations - Hickory, NC (Onsite) ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients ...

Contract Senior Clinical Research Associate - Home-Based (US) ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to ...

Contract Senior Clinical Research Associate - Home-Based (US) ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to ...

Senior Clinical Research Associate - Neurovascular - Midwest/Central ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive ...

Senior Clinical Research Associate ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and ...

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$49K

$107.3K

$189K

How much do icon clinical research jobs pay per year?

As of Jun 11, 2026, the average yearly pay for icon clinical research in the United States is $107,336.00, according to ZipRecruiter salary data. Most workers in this role earn between $81,000.00 and $122,500.00 per year, depending on experience, location, and employer.

Which is better, IQVIA or ICON?

Both IQVIA and ICON are leading contract research organizations (CROs) that provide clinical trial services, including site management, data analysis, and regulatory support. The choice between them depends on specific project needs, geographic presence, and client preferences, rather than a clear overall superiority. For job seekers, understanding each company's culture, project types, and required skills can help determine the best fit for a clinical research role.

How much does Icon clinical research pay?

The average salary for an Icon Clinical Research employee varies by role and experience, with clinical research associates earning approximately $70,000 to $90,000 annually. Entry-level positions may start around $50,000, while more experienced professionals or those in managerial roles can earn over $100,000. Compensation often includes benefits such as health insurance and performance bonuses.

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

To thrive at ICON Clinical Research, you typically need a background in life sciences or a related field, experience with clinical trial processes, and strong analytical skills. Familiarity with industry-standard clinical trial management systems (CTMS), electronic data capture (EDC) platforms, and certifications such as GCP (Good Clinical Practice) are highly valued. Excellent organizational skills, attention to detail, and effective communication help you excel in a collaborative research environment. These skills are crucial to ensure regulatory compliance, data integrity, and successful execution of clinical trials.

What is the controversy with ICON plc?

As a clinical research organization, ICON plc has faced scrutiny over issues such as regulatory compliance and data integrity in some trials. However, it remains a major player in the industry, employing professionals with skills in Good Clinical Practice (GCP) and regulatory standards. The company continues to operate under strict industry regulations to ensure trial quality and patient safety.

Is ICON a good company to work for?

Icon Clinical Research is a well-known contract research organization in the clinical trials industry, offering roles such as clinical research associate and project manager. Employees often cite competitive pay, opportunities for professional development, and a collaborative work environment, though experiences can vary by location and role.

What does a typical day look like for someone working at ICON Clinical Research?

A typical day at ICON Clinical Research often involves collaborating with cross-functional teams to oversee the progress of clinical trials, monitoring study data for accuracy, and ensuring all activities adhere to regulatory standards. You'll attend project meetings, communicate regularly with sponsors and investigators, and manage documentation and reporting tasks using specialized software. Depending on your specific role, you may also be responsible for site management, participant enrollment, or clinical data review. The work environment is fast-paced and supportive, offering opportunities for professional growth and advancement within the clinical research field.

What is an Icon Clinical Research job?

An ICON Clinical Research job typically involves working for ICON plc, a global provider of outsourced development and commercialization services to pharmaceutical, biotechnology, and medical device companies. Roles at ICON can range from clinical research associates and project managers to data analysts and regulatory specialists. Employees help design, manage, and monitor clinical trials to ensure they meet regulatory and ethical standards. These positions often require experience in clinical research, strong attention to detail, and adherence to Good Clinical Practice (GCP) guidelines.

What cities are hiring for Icon Clinical Research jobs? Cities with the most Icon Clinical Research job openings:
What are the most commonly searched types of Icon Clinical Research jobs? The most popular types of Icon Clinical Research jobs are:
What states have the most Icon Clinical Research jobs? States with the most job openings for Icon Clinical Research jobs include:
Infographic showing various Icon Clinical Research job openings in the United States as of June 2026, with employment types broken down into 3% Internship, 6% Full Time, 75% Part Time, 3% Temporary, 10% Contract, and 3% Nights. Highlights an 89% Physical, 3% Hybrid, and 8% Remote job distribution, with an average salary of $107,336 per year, or $51.6 per hour.
Team Lead, Site Operations (Oncology)

Team Lead, Site Operations (Oncology)

ICON

Lisle, IL โ€ข On-site

$68K - $85K/yr

Full-time

Medical, Dental, Vision, Life, Retirement

Posted 8 days ago


Job description

Team Lead, Site Operations (Oncology) - Lisle, IL (Onsite - multiple locations)
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 have an exciting opportunity for a Team Lead, Site Operations to join ICON's Accellacare team. As a Team Lead, you will lead a team responsible for supporting site-facing activities across clinical studies, with a primary focus in Oncology (Phase II-IV), ensuring consistent, high-quality operational delivery.
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 network is designed with one goal in mind: to deliver better access, greater efficiency, and improved outcomes in clinical research.
Location: 100% Onsite at Accellacare Duly Health & Care (multiple sites around Lisle, IL)
Hours: Monday - Friday; 8:00am - 5:00pm (no weekends or holidays)
What You Will Be Doing:
  • Supervising a team of site operations staff (e.g., Clinical Research Coordinators, Clinical Research Nurses), overseeing daily workloads and priorities
  • Ensuring timely and accurate completion of site start-up, maintenance, and close-out tasks in line with SOPs and study plans
  • Monitoring site operations metrics and contributing to actions that improve efficiency and site experience
  • Collaborating with project management, monitoring, and other functions to resolve site-related issues
  • Supporting training, development, and performance management of team members
  • Contributing to the enhancement of site operations processes, tools, and documentation

Your Profile:
  • Oncology Clinical Research industry experience
  • 3+ years of experience in clinical site operations, site support, or clinical operations
  • Prior lead or mentoring responsibilities preferred
  • Good understanding of clinical trial processes, GCP, and site documentation requirements
  • Strong leadership, communication, and organizational skills
  • Ability to manage multiple studies and priorities in a fast-paced environment
  • Collaborative, solution-oriented mindset with focus on quality and customer service
  • Bachelor's degree in life sciences, healthcare, business, or a related field

#LI-TP1
#LI-Accellacare
#LI-Onsite
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
$68,616.00-$85,770.00
Are you a current ICON Employee? Please click here to apply