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Icon Clinical Research Jobs (NOW HIRING)

ICON

Clinical Research Administrator

Lisle, IL · On-site

$38K - $48K/yr

Associate Clinical Research Coordinator - Lisle, IL (Onsite, multiple locations) ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines ...

Icon plc

Clinical Research Administrator

Lombard, IL · On-site

$38K - $48K/yr

Associate Clinical Research Coordinator - Lisle, IL (Onsite, multiple locations) ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines ...

Icon plc

Clinical Research Administrator

Lisle, IL · On-site

$38K - $48K/yr

Associate Clinical Research Coordinator - Lisle, IL (Onsite, multiple locations) ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines ...

Icon plc

Clinical Research Administrator

Winfield, IL · On-site

$38K - $48K/yr

Associate Clinical Research Coordinator - Lisle, IL (Onsite, multiple locations) ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines ...

Icon plc

Clinical Research Administrator

Oak Lawn, IL · On-site

$38K - $48K/yr

Associate Clinical Research Coordinator - Lisle, IL (Onsite, multiple locations) ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines ...

Icon plc

Clinical Research Administrator

Downers Grove, IL · On-site

$38K - $48K/yr

Associate Clinical Research Coordinator - Lisle, IL (Onsite, multiple locations) ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines ...

Icon plc

Clinical Research Coordinator Level 1

Lombard, IL · On-site

$23.75 - $31.75/hr

Clinical Research Coordinator Level 1 - Lombard, IL (Onsite) ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to ...

ICON

Senior Clinical Research Coordinator (Oncology)

Lisle, IL · On-site

$24 - $31.75/hr

Senior Clinical Research Coordinator (Oncology) - Lisle, IL (Onsite - multiple locations) ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new ...

ICON Clinical Research

Site Care Partner

Site Care Partner - US 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 ...

ICON Clinical Research

Country Lead Monitor

Raleigh, NC · On-site

Country Lead Monitor 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 ...

ICON Clinical Research

Medical Monitor

Lenexa, KS · On-site

Medical Monitor 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 ...

Icon plc

Clinical Research Coordinator

Blue Bell, PA · On-site

$23.25 - $30.75/hr

Clinical Research Coordinator- McComb, MS ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As ...

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Icon Clinical Research information

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$49K

$107.3K

$189K

How much do icon clinical research jobs pay per year?

As of Sep 3, 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.

What is an Icon Clinical Research?

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 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 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.

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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?

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What states have the most Icon Clinical Research jobs?

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Icon Clinical Research jobs near you
Infographic showing various Icon Clinical Research 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 $107,336 per year, or $51.6 per hour.

Clinical Research Administrator

ICON

Lisle, IL • On-site

$38K - $48K/yr

Full-time

Medical, Dental, Vision, Life, Retirement

Posted 22 days ago

Job description

Associate Clinical Research Coordinator - 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 incredible opportunity for a Clinical Research Administrator to join ICON's Accellacare team. The Administrator is an integral part of the team providing administrative support, calendar management, and supporting Clinical Research Coordinators for clerical assigned tasks in according with SOPs and ICH-GCP.
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: Full-Time Onsite at Accellacare Duly Health & Care (Primary Site:
430 Warrenville Rd Lisle, IL 60532 but will travel to sites in Lombard, Winfield, and Oak Lawn, IL)
Hours: Monday - Friday; 8:00am - 5:00pm (no weekends or holidays)
What you will be doing:
  • Responsible for the day-to-day coordination and administration of the clinical research site
  • Ensuring patient notes are ready for the following day's schedule
  • Complete training on Clinical Trial Management System and maintain skills to update the database, complete participant reimbursement, capture referral source of participants, and create call lists to promote recruitment
  • Ensure all study visits are scheduled appropriately and within visit windows determined by individual protocols
  • Responsible for reception, answering calls, and placing appointment reminder calls to patients
  • Ensuring the site is a welcoming environment for patients and that patients are treated with dignity and privacy
  • Supporting the Site Manager with services coordination such as vendor management, purchasing, and supply management
  • Responsible for processing patient payments and site related invoices
  • Assisting the Clinical Research Coordinators with documentation and data entry/queries
  • May assist with laboratory duties such as performing quality assurance review, restocking of supplies, and processing of specimens
  • Assisting the Clinical Research Coordinators or other staff members with creating and copying patient files for study closeout procedures
  • Travel to multiple Duly Health & Care sites within the Accellacare network

Your Profile:
  • 6+ months of administrative or clerical experience
  • Experience in a healthcare setting (preferred)
  • Strong organizational skills and attention to detail, with the ability to manage multiple tasks and priorities effectively
  • Excellent communication and interpersonal skills, with the ability to interact professionally with study participants and colleagues
  • Proficiency in Microsoft Office suite (Word, Excel, Outlook) and willingness to learn new software applications as needed
  • Associates Degree

#LI-Office
#LI-TP1
#LI-Accellacare
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
$38,728.00-$48,410.00
Are you a current ICON Employee? Please click here to apply

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