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Summer 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 · 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 ...

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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 ...

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

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 plc

Clinical Research Coordinator Level 1

Lombard, IL

$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 ...

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Summer Icon Clinical Research information

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

As of Aug 23, 2026, the average hourly pay for summer icon clinical research in the United States is $24.09, according to ZipRecruiter salary data. Most workers in this role earn between $20.19 and $24.76 per hour, depending on experience, location, and employer.

What is a Summer Icon Clinical Research position?

A Summer Icon Clinical Research position is typically an internship or temporary role offered during the summer months, where students or recent graduates work alongside experienced clinical researchers. The position involves participating in various stages of clinical trials, such as data collection, patient interaction, regulatory documentation, and analysis. These roles are designed to provide hands-on experience in clinical research, helping participants develop an understanding of clinical trial protocols, ethical considerations, and research methodologies. Summer Icon Clinical Research positions are valuable for those considering a career in medicine, pharmaceuticals, or scientific research.

What are the key skills and qualifications needed to thrive as a clinical research associate, and why are they important?

To thrive as a Clinical Research Associate, you need a solid understanding of clinical trial protocols, regulatory guidelines, and typically hold a degree in life sciences or a related field. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) tools, and certifications like GCP (Good Clinical Practice) are common requirements. Attention to detail, strong organizational skills, and effective communication make a candidate stand out in this role. These skills ensure accurate data collection, compliance with regulations, and successful coordination among research teams and study sites.

What are some common challenges faced by clinical research interns during a summer program, and how can they prepare for them?

Clinical research interns in summer programs often encounter challenges such as quickly adapting to complex regulatory protocols, managing large volumes of data, and balancing multiple tasks within tight timelines. To prepare, it's helpful to review basic clinical research methodologies, develop strong organizational skills, and familiarize yourself with commonly used software like REDCap or Excel. Proactive communication with supervisors and team members can also help clarify expectations and ensure smooth collaboration throughout the internship.

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

AspectSummer Icon Clinical ResearchSummer Icon Clinical Research Coordinator
Primary RoleAssists in clinical trial activities, data collection, and site supportManages patient recruitment, schedules, and ensures protocol adherence
Required CredentialsTypically no formal certification, relevant coursework helpfulOften requires relevant healthcare or research certifications
Work EnvironmentResearch sites, laboratories, or clinical settingsClinical sites, hospitals, or research facilities
Employer & Industry UsagePharmaceutical companies, research institutionsHospitals, clinics, research organizations

In summary, Summer Icon Clinical Research roles focus on supporting clinical trials through data and site assistance, while Summer Icon Clinical Research Coordinators take on more responsibility in managing patient interactions and trial logistics. Both roles are essential in the clinical research process but differ in scope and responsibilities.

More about Summer Icon Clinical Research jobs

What cities are hiring for Summer Icon Clinical Research jobs?

Cities with the most Summer 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 Summer Icon Clinical Research jobs?

States with the most job openings for Summer Icon Clinical Research jobs include:

What job categories do people searching Summer Icon Clinical Research jobs look for?

The top searched job categories for Summer Icon Clinical Research jobs are:

Summer Icon Clinical Research jobs near you
Infographic showing various Summer 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 $50,108 per year, or $24.1 per hour.

Clinical Research Administrator

ICON

Lisle, IL • On-site

$38K - $48K/yr

Full-time

Medical, Dental, Vision, Life, Retirement

Posted 11 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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