Senior Clinical Research Coordinator - Glenview, IL (Onsite, Part-Time Contractor)
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 part-time, contract opportunity for a Senior Clinical Research Coordinator, onsite in Glenview, IL.
Location: Glenview, IL 60026
Hours : Part Time (maximum 20 hours / week)
Schedule : Candidates must be flexible to work a changing schedule during standard business hours, Monday through Friday
Hiring Model : Independent Contractor, 1099
Contract Duration : 6 months
What You Will Do:
As a Senior CRC, you will coordinate and manage the operational aspects of clinical trials, including participant recruitment, scheduling, and site logistics, ensuring adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards throughout the trial.
Key responsibilities include:
Support day-to-day clinical trial activities, including pre-screening, recruitment, and participant-related study activities, as applicable
Conduct the informed consent process and educate participants on study requirements and procedures
Review inclusion/exclusion criteria and support patient screening and enrollment
Perform timely and accurate clinical trial data entry within CTMS and EMR systems and resolve data queries in accordance with study requirements
Collaborate with investigators, monitors, and study team members to support effective study conduct, including monitoring visits and investigator meetings
Maintain accurate and complete study-related documentation and information in applicable study systems
Communicate patient status, recruitment progress, study needs, and safety information to investigators and study leadership
Support protocol-mandated study visits and procedures, as applicable, excluding investigational product dosing and unblinded IP accountability
Partner with investigators and the study team to support regulatory requirements and overall study execution
Required qualifications and experience:
2+ years of experience as a Clinical Research Coordinator
Experience with EPIC or another comparable EMR
Experience with Medidata Rave or another CTMS
Good understanding of clinical trial processes, GCP, and site documentation requirements
Excellent time management and planning skills with an organized approach to work
Bachelor’s degree in life sciences, healthcare, or a related field
Preferred qualifications and experience:
Experience with Phase III and / or Cardiology trials
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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
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