New · posted Nov 13
ICON · Pharmaceuticals
Senior Clinical Research Coordinator
- Glenview, IL
- On-site
- Contract
- Senior & Principal
The role
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 need
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 experiencenice to have
- Experience with Phase III and / or Cardiology trials
Employment with ICON is contingent upon having the legal right to work in the country where the role is based.
What you'll 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
Pay and benefits
ICON didn't publish pay for this role
See what similar roles pay on Regulatory Jobs, or try the salary calculator.
-
Are you a current ICON Employee? Please click here to apply
Rewards & Benefits
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
ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.
Benefits may include:
Benefits may vary depending on role and location.
Visit our careers site to read more about the benefits ICON offers.
Where you'll work
Glenview, ILOn-siteOpen in Maps (opens in a new tab)
More jobs in Glenview, ILEqual opportunity, accessibility and legal noticesICON's statements, word for word
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.
Job intelligence
The context around this role
Live data · November 13, 2026
Salary intelligence
How the pay compares
Senior & Principal roles in the US65 roles publishing pay
| Annual base pay | Low | Median | High |
|---|---|---|---|
| All US (middle half) | $110,000 | $124,500 | $125,500 |
Comparisons: the base pay employers published on open Clinical Research roles at the same level on Regulatory Jobs, November 13, 2026. Nothing is estimated.
Career trajectory
Where this role sits in Clinical Research
The general path across 260 open Clinical Research roles on Regulatory Jobs, with the titles they carry most. Not ICON's own promotion track.
Skills DNA
What this role leans on
How many of the posting's 27 duty, requirement and summary lines touch each area. The posting's emphasis, not a proficiency score.
- Clinical trial conduct14
- Documentation and SOPs4
- Investigations and CAPA4
- Collaboration and leadership4
- GMP and compliance2
- Quality systems and risk1
- Data and digital systems1
Regulatory intelligence
The rules, regulations and standards behind this role
The regulations, guidance and standards that govern Clinical Research work in pharmaceuticals, led by the one this posting names, each linked to the agency or standards body that publishes it.
- ICHICH E6(R3) good clinical practice(official source, opens in a new tab)The international standard for the design, conduct and reporting of clinical trialsNamed in the posting
- FDA21 CFR Part 312(official source, opens in a new tab)Investigational New Drug applications and sponsor duties in drug trials
- FDA21 CFR Part 50(official source, opens in a new tab)Protection of human subjects: informed consent in FDA-regulated trials
- FDA21 CFR Part 56(official source, opens in a new tab)Institutional review boards for FDA-regulated clinical investigations
- EUEU Clinical Trials Regulation 536/2014(official source, opens in a new tab)How clinical trials of medicines are authorized and run in the EU, through CTIS
- ICHICH E8(R1)(official source, opens in a new tab)General considerations for clinical studies and quality by design in trials
- HHS45 CFR Part 46 (Common Rule)(official source, opens in a new tab)The federal policy for the protection of human research subjects
- NIH42 CFR Part 11(official source, opens in a new tab)Clinical trial registration and results reporting on ClinicalTrials.gov
- FDAFDA Bioresearch Monitoring (BIMO)(official source, opens in a new tab)FDA inspections of clinical investigators, sponsors, IRBs and GLP labs
- FDA21 CFR Part 11(official source, opens in a new tab)FDA rules for electronic records and electronic signatures
- HHSHIPAA Privacy Rule(official source, opens in a new tab)Federal protections for individually identifiable health information
- EUGDPR (Regulation 2016/679)(official source, opens in a new tab)The EU General Data Protection Regulation for personal data, including health data
- ICHICH E9 and E9(R1)(official source, opens in a new tab)Statistical principles for clinical trials and estimands
- FDA21 CFR 314.80 and 600.80(official source, opens in a new tab)Postmarketing reporting of adverse drug and biologic experiences
- ICHICH E2A to E2F(official source, opens in a new tab)Clinical safety data management, expedited reporting and periodic safety reports
- ICHMedDRA(official source, opens in a new tab)The ICH medical terminology for coding adverse events and medical history
Company hiring pulse
ICON on Regulatory Jobs
- 168
- Open roles
- 168
- Distinct roles
- 39
- Locations
By discipline
- Clinical162 92%
- Quality11 6%
- Regulatory4 2%
By level
- Associate & Specialist77 44%
- Senior & Principal70 40%
- Manager23 13%
More roles at ICON
- View role
Clinical Research Associate I
United StatesAssociate & SpecialistPharmaceuticalsSalary not listed
- View role
Clinical Research Associate
Remote, USAssociate & SpecialistPharmaceuticalsSalary not listed
- View role
CRA I, Lab Technologist
United StatesAssociate & SpecialistPharmaceuticalsSalary not listed
- View role
CRA I, Lab Technologist
Remote, USAssociate & SpecialistPharmaceuticalsSalary not listed
Similar Clinical Research roles elsewhere
- View role
Experienced Clinical Research Associate (CRA II/Sr CRA)
Thermo Fisher ScientificRemote, USSenior & PrincipalPharmaceuticals$67K–$125K
- View role
Clinical Research Physician Investigator - Part Time
Thermo Fisher ScientificSan Antonio, TXSenior & PrincipalPharmaceuticalsSalary not listed
- View role
Senior Clinical Research Associate (US-West) - FSP
ParexelRemote, USSenior & PrincipalPharmaceuticalsSalary not listed
- View role
Sr. Clinical Research Associate - Early Phase Studies (Las Vegas, NV)
Thermo Fisher ScientificLas Vegas, NV · HybridSenior & PrincipalPharmaceuticalsSalary not listed
Senior Clinical Research Coordinator at ICON
Open until filled.