Clinical Research Coordinator- Chicago, IL
About The Position
The Clinical Research Division at The IMA Group is a dynamic hub of expertise and innovation, dedicated to advancing healthcare through clinical trials and studies. Our team of seasoned professionals collaborates with industry leaders, conducting patient-centric research across diverse therapeutic areas. Committed to ethical practices and regulatory compliance, we aim to pioneer groundbreaking medical solutions that shape the future of healthcare. IMA Clinical Research is seeking an experienced Clinical Research Coordinator with a strong background in managing clinical trials and proficiency in phlebotomy. We are especially interested in candidates with experience in CNS (Central Nervous System) studies, psychiatry, psychology, or social work. This full-time position is based in Chicago, IL, with an annual salary range of $60,000 - $65,000, depending on experience.
Requirements
- Previous clinical experience in a healthcare or research setting preferred.
- Proficient in conducting and interpreting clinical and diagnostic assessments (vital signs, height, weight, temperature, etc.).
- Demonstrated ability to work independently, lead studies, and make informed decisions.
- Strong teamwork, communication, and problem-solving skills with a professional demeanor and high motivation.
- Minimum of two years of clinical research and phlebotomy experience.
- Bachelor’s degree required; Master’s degree or equivalent experience preferred.
- Proven ability to manage multiple concurrent studies.
Nice To Haves
- Clinical Research Coordinator certification (CCRC) preferred.
- Experience in CNS research, psychiatry, psychology, or social work is highly desirable.
Responsibilities
- Coordinate clinical trials according to sponsor protocols and ensure adherence to SOPs.
- Acquire and maintain comprehensive knowledge of study protocols and associated procedures.
- Communicate effectively with sponsors, CROs, CRAs, IRBs, laboratories, and clinical personnel.
- Advise Investigators and staff on study protocols and procedures essential for successful study execution.
- Ensure timely documentation and reporting of adverse or serious adverse events in accordance with protocol.
- Uphold ALCOA principles for accurate and timely documentation, including meticulous data entry.
Benefits
- Complete Health Coverage: Comprehensive Health, Dental, and Vision Insurance packages to ensure your well-being.
- Balanced Lifestyle: Generous paid time off, holidays, and a floating holiday to maintain a healthy work-life balance.
- Retirement: A 401k plan with employer matching for a secure financial future.
- Comprehensive Benefit Offerings: Benefits include LTD, STD, Flexible Spending Account, Voluntary Life, Voluntary ADD, and Company-paid Life Insurance and ADD coverage.
- Tuition Assistance and Student Loan Repayment Assistance: Benefit from IMA’s tax free tuition reimbursement and tax-free student loan repayment assistance program to fuel your ongoing educational journey and to help you pay for the degree you already have!
- Family Support: Paid maternity leave and paid parental leave reflecting our commitment to supporting families.
- No on Call Responsibilities: When you are home, you can leave work behind.
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What This Job Offers
Job Type
Full-time
Career Level
Mid Level
Number of Employees
501-1,000 employees
