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Volunteer 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 ...

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Clinical Research Administrator

Lisle, IL

$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 ...

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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 ...

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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

Clinical Research Coordinator Level 1

Lombard, IL · On-site

$23.75 - $31.75/hr

We have an incredible opportunity for a Clinical Research Coordinator 1 to join ICON's Accellacare team. The CRC 1 ensures the safety of our volunteers, promotes the mission of Accellacare, and ...

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Clinical Research Coordinator Level 1

Lombard, IL

$23.75 - $31.75/hr

We have an incredible opportunity for a Clinical Research Coordinator 1 to join ICON's Accellacare team. The CRC 1 ensures the safety of our volunteers, promotes the mission of Accellacare, and ...

ICON

Patient Recruitment Associate I

Winston Salem, NC · On-site

Patient Recruitment Associate ICON is a global healthcare intelligence and clinical research ... Identify appropriate study opportunities for interested volunteers based on knowledge of clinical ...

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Volunteer Icon Clinical Research information

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$15

$28

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How much do volunteer icon clinical research jobs pay per hour?

As of Aug 21, 2026, the average hourly pay for volunteer icon clinical research in the United States is $28.69, according to ZipRecruiter salary data. Most workers in this role earn between $23.32 and $31.01 per hour, depending on experience, location, and employer.

What is a volunteer in clinical research at ICON?

Volunteer Icon Clinical Research roles typically involve participating in clinical trials as a volunteer at Icon, a global clinical research organization. Volunteers help advance medical science by testing new drugs, treatments, or medical devices under carefully controlled conditions. These roles are crucial for ensuring that new therapies are safe and effective before they become widely available to the public. Volunteers may be compensated for their time and travel, and their participation directly contributes to the development of future medical treatments.

What can I expect from the onboarding process as a volunteer in clinical research at ICON?

As a volunteer at Icon Clinical Research, the onboarding process typically involves an initial screening to assess eligibility, followed by a comprehensive orientation about the study's requirements and procedures. You will receive detailed information on your rights, potential risks, confidentiality, and the study timeline. The medical team will guide you through informed consent and answer any questions to ensure you are comfortable before participation. Throughout the study, you will collaborate closely with research staff and may need to attend scheduled visits for assessments or sample collections.

What are the key skills and qualifications needed to thrive as a volunteer in clinical research at ICON?

To thrive as a Volunteer in Clinical Research at ICON, you generally need to meet basic eligibility criteria such as good health, reliability, and clear communication skills, with no specific formal qualifications required. Familiarity with study protocols, informed consent procedures, and adherence to clinical trial guidelines is important, though most technical training is provided by the research team. Dependability, attention to detail, and the ability to follow instructions are valuable soft skills for this role. These qualities ensure the integrity of study data, participant safety, and the overall success of the research process.

What is the difference between Volunteer Icon Clinical Research vs Clinical Research Coordinator?

AspectVolunteer Icon Clinical ResearchClinical Research Coordinator
CredentialsTypically no formal credentials required; some knowledge of clinical trialsOften requires a bachelor's degree in health sciences or related field; certification preferred
Work EnvironmentVolunteer settings, research sites, hospitalsResearch sites, hospitals, clinics
Employer & IndustryNon-profit organizations, research institutions, pharmaceutical companiesHospitals, research organizations, pharmaceutical companies
Search & Comparison IntentUnderstanding volunteer roles in clinical researchExploring professional roles and responsibilities in clinical trials

Volunteer Icon Clinical Research roles are typically volunteer-based with minimal formal credentials, focusing on assisting research activities. Clinical Research Coordinators are paid professionals with relevant education and certifications, responsible for managing clinical trial processes. Both work in research environments but differ mainly in qualifications and employment status.

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Volunteer Icon Clinical Research jobs near you
Infographic showing various Volunteer Icon Clinical Research job openings in the United States as of August 2026, with employment types broken down into 4% As Needed, 70% Full Time, 17% Part Time, and 9% Contract. Highlights an 94% Physical, 1% Hybrid, and 5% Remote job distribution, with an average salary of $59,666 per year, or $28.7 per hour.

Clinical Research Administrator

ICON

Lisle, IL • On-site

$38K - $48K/yr

Full-time

Medical, Dental, Vision, Life, Retirement

Posted 10 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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