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60 Icon Clinical Trial Associate Jobs Hiring Near You

Associate Clinical Research Coordinator - Lisle, IL (Onsite, multiple locations) ICON is a global ... Complete training on Clinical Trial Management System and maintain skills to update the database ...

Clinical Operations Manager - Regulatory - Montreal ICON is a global healthcare intelligence and ... Executes and oversees clinical trial country submissions and approvals for assigned protocols.

EDC Clinical Trial Designer 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 ...

Clinical Operations Manager - Regulatory - Montreal ICON is a global healthcare intelligence and ... Executes and oversees clinical trial country submissions and approvals for assigned protocols.

Senior Clinical Research Associate- Northeast ICON is a global healthcare intelligence and clinical ... As a Senior CRA at ICON Plc, you will oversee and manage clinical trial activities to ensure they ...

Associate Clinical Research Coordinator - Lisle, IL (Onsite, multiple locations) ICON is a global ... Complete training on Clinical Trial Management System and maintain skills to update the database ...

Associate Clinical Research Coordinator - Lisle, IL (Onsite, multiple locations) ICON is a global ... Complete training on Clinical Trial Management System and maintain skills to update the database ...

Associate Clinical Research Coordinator - Lisle, IL (Onsite, multiple locations) ICON is a global ... Complete training on Clinical Trial Management System and maintain skills to update the database ...

Senior Clinical Research Associate- Northeast ICON is a global healthcare intelligence and clinical ... As a Senior CRA at ICON Plc, you will oversee and manage clinical trial activities to ensure they ...

Study Start Up Associate II

Pittsburgh, PA · On-site

$32.50 - $44.50/hr

Study Start-Up Specialist (Sponsor Dedicated) ICON is a global healthcare intelligence and clinical ... Must have knowledge of clinical trial conduct * General knowledge of drug development and ICH/GCP ...

Study Start Up Associate II

North Wales, PA · On-site

$32.50 - $44.25/hr

Study Start-Up Specialist (Sponsor Dedicated) ICON is a global healthcare intelligence and clinical ... Must have knowledge of clinical trial conduct * General knowledge of drug development and ICH/GCP ...

Study Start Up Associate II

Cary, NC · On-site

$31 - $42.50/hr

Study Start-Up Specialist (Sponsor Dedicated) ICON is a global healthcare intelligence and clinical ... Must have knowledge of clinical trial conduct * General knowledge of drug development and ICH/GCP ...

Clinical Research Associate - Multi TA ICON is a global healthcare intelligence and clinical ... As a CRA at ICON Plc, you will play a critical role in overseeing and managing clinical trial ...

As a Senior CRA at ICON Plc, you will oversee and manage clinical trial activities to ensure they ... Extensive experience as a Clinical Research Associate, with a strong understanding of clinical ...

Study Start Up Associate II

Philadelphia, PA · On-site

$33.75 - $46.25/hr

Study Start-Up Specialist (Sponsor Dedicated) ICON is a global healthcare intelligence and clinical ... Must have knowledge of clinical trial conduct * General knowledge of drug development and ICH/GCP ...

Showing results 21-40

Clinical Research Administrator

Icon plc

Lisle, IL • On-site

$38K - $48K/yr

Full-time

Medical, Dental, Vision, Life, Retirement

Posted 26 days ago


Key responsibilities

  • Coordinate and administer daily activities at the clinical research site, including scheduling and ensuring patient notes are prepared.

  • Support Clinical Research Coordinators with documentation, data entry, and other clerical tasks according to SOPs and ICH-GCP.

  • Assist with site operations such as vendor management, supply management, processing patient payments, and supporting study closeout procedures.


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 requesthere.

Salary Range

$38,728.00-$48,410.00

Are you a current ICON Employee? Please click here to apply