Clinical Research Coordinator – Metabolic & Gen Med Clinical Trials - Chicago, IL
The IMA Group
- Chicago, Illinois
- 4 days ago
- $60,000–$65,000 Per Year
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Skills
- Adverse Eventsunmatched
- Behavioral Healthunmatched
- Certified Clinical Research Coordinator (CCRC)unmatched
- Clinical Researchunmatched
- Clinical Trialunmatched
- Clinical Trial Managementunmatched
- Contract Research Organization (CRO)unmatched
- Documentationunmatched
- Endocrinologyunmatched
- Federal Governmentunmatched
- GCP (Good Clinical Practices)unmatched
- Governmentunmatched
- Institute of Management Accountants (IMA)unmatched
- Internal Medicineunmatched
- Medical Researchunmatched
- Medicineunmatched
- Multitaskingunmatched
- Needs Assessmentunmatched
- Organizational Skillsunmatched
- Patient Careunmatched
- Phase II Clinical Trialsunmatched
- Phase IV Clinical Trialsunmatched
- Phlebotomyunmatched
- Psychologyunmatched
- Quality Managementunmatched
- Quality Metricsunmatched
- Regulationsunmatched
- Sample/Specimen Processingunmatched
- Specimens/Samplesunmatched
- Startupunmatched
- Worker's Compensationunmatched
Description
Description
Clinical Research Coordinator – Clinical Trials
Chicago, IL | Full-Time | Permanent | $60,000–$65,000 Depending on Experience
Ready to make a meaningful impact in clinical research? IMA Clinical Research is seeking an experienced Clinical Research Coordinator to join our Chicago team and play a key role in advancing new therapies and improving patient outcomes.
In this role, you’ll help manage clinical trials from start-up through closeout while working directly with study participants and collaborating with investigators, sponsors, CROs, and monitors. You’ll be part of a team dedicated to maintaining the highest standards of quality, compliance, and participant care.
What You’ll Do:
- Coordinate participant visits, assessments, and follow-up appointments
- Manage study activities across multiple clinical trials
- Perform venipuncture and process laboratory specimens
- Maintain accurate source documentation and regulatory files in accordance with GCP and sponsor requirements
- Support participant recruitment, enrollment, retention, and education
- Identify and report adverse events while maintaining study quality standards
What You’ll Bring:
- 2+ years of experience as a Clinical Research Coordinator
- Strong phlebotomy skills
- Bachelor's degree required; advanced degree preferred
- Experience with metabolic, endocrine, internal medicine, or related therapeutic studies preferred
- Ability to manage multiple priorities in a fast-paced environment
- CCRC certification welcomed but not required
Why Join IMA Clinical Research?Enjoy a full-time, permanent career with competitive benefits, including medical, dental, vision, 401(k) with company match, PTO, paid holidays, tuition reimbursement, student loan repayment assistance, and paid parental leave.
No nights, weekends, or on-call requirements.
Join us in advancing medical research—one study and one participant at a time.
The IMA Group is an Affirmative Action/Equal Opportunity Employer
Our Government Services Division supports local, state, and federal agencies and delivers professional and objective medical and psychological examinations as well as ancillary services. Our Payer Services Division meets the evaluation and screening needs of Carriers, TPAs, Public Entities and Employers and includes behavioral health and physical medicine specialty services, working with a wide range of organizations within the workers' compensation, disability, liability, and auto markets. Our Clinical Research Division performs all types of Phase II-IV clinical trials in multiple therapeutic areas through a flexible nationwide network of site locations and virtual capabilities.
#LI-EG1 #LI-ONSITE
Numbers & Facts
| Location | Chicago, Illinois |
| Industry | Healthcare Services |
| Salary | $60,000–$65,000 Per Year |
| Company Size | 500 to 999 employees |
| Year Founded | 1990 |
| Website | http://www.ima-us.com |
About Company
About The IMA Group
Headquartered in Tarrytown, New York, with its main operations center in Albany, New York, The IMA Group is a national leader with a reputation for providing high-quality medical, psychological and speech and language evaluations. IMA's primary areas of focus are Social Security Disability Consultative Examinations, VA Compensation and Pension Exams, Employability Evaluations, and Occupational Health Services. Our clients include local, state, and federal agencies, as well as private insurers and corporations.
Dr. David Pulver, IMA's President and CEO, is a Board Certified Internist with over thirty years of experience performing disability exams for Social Security Disability. Dr. Pulver has overseen IMA's growth from a single office in White Plains, NY in 1990, to its present status, with over 45 offices throughout New York, Pennsylvania, District of Columbia, Florida, Ohio, New Jersey, Connecticut, Missouri, Virginia and Vermont. Over the past 25 years, IMA has conducted more than 2.5 million evaluations and has grown to a network of more than 500 licensed providers.
IMA Research is a multi-site research company specializing in Phase II, III and IV studies in all primary care disciplines, co-located within many of our facilities. View IMA Research Site
IMA provides a full range of services, including:
Social Security Disability Consultative Examinations VA Compensation and Pension (C & P) Exams Employability Evaluations Substance Abuse Assessments and Monitoring (SAAM) Case Review Occupational Health Evaluations Police Officer/Firefighter Pre-employment Evaluations and Testing Independent Medical Examinations (IME's) (View Our IME Referral Form) Fitness for Duty Exams (FFD) DOT Physicals including Drug and BAT Testing Vocational Rehabilitation Evaluations