Clinical Research Coordinator II-Heart Center
The Clinical Research Coordinator II at Confidential Client coordinates and manages clinical research studies focused on pediatric heart care, ensuring regulatory compliance and ethical conduct. This role balances patient-facing activities with administrative tasks, including study documentation, participant engagement, data collection, and coordination across departments to support high-quality research outcomes.
About Careertakes
👉 Important disclosure: Careertakes is a third-party recruiting platform supporting this hiring process. If selected, you will be employed directly by our client, Admin.
Applicants for this role may also receive access to additional matched opportunities through the Careertakes platform.
What You’ll Do
Confidential Client is hiring a Clinical Research Coordinator II to support pediatric clinical research activities in Chicago, IL. In this role you will coordinate study execution, maintain regulatory compliance, and serve as a primary patient/study liaison across multiple clinical trials.
- Coordinate study start-up, regulatory submissions, and required approvals (IRB/sponsor).
- Maintain regulatory binders, source documents, and study correspondence to ensure protocol compliance.
- Schedule and conduct clinical research visits, site qualifications, initiation, monitoring, and close-out activities.
- Collect, process, and document specimens; assist with QA/QC and data validation.
- Screen and recruit participants, obtain informed consent, verify eligibility, and manage participant communications and reimbursements.
- Prepare study supplies, lab kits, and requisitions; manage equipment and inventory.
- Track deadlines for grants, deliverables, and study milestones.
- Abstract and code study data; develop data dictionaries and codebooks to support downstream analysis.
- Attend investigator meetings, present findings, and support educational and ethical research initiatives.
- Support invoicing and billing tasks related to study finances.
- Perform other duties as assigned to support the research team.
Who You Are (Qualifications)
- Bachelor’s degree plus at least one year of clinical research experience, or equivalent combination of education and directly related experience.
- Working knowledge of FDA, HSR, and GCP guidelines.
- Strong organizational skills with the ability to manage multiple studies and competing priorities.
- Clear verbal and written communication skills; effective patient-facing presence.
- Analytical skills to support quantitative and qualitative research tasks and familiarity with common research technologies.
- Entry-level leadership skills; able to collaborate effectively and foster an inclusive team environment.
Compensation & Benefits
- Pay range: $49,920.00 – $81,619.20 per year (Confidential Client provides competitive compensation aligned with experience and internal equity).
- Benefits for full- and part-time employees (20+ hours/week) may include:
- Medical, dental, and vision insurance
- Employer-paid group term life and disability
- Employer contribution to Health Savings Account
- Flexible Spending Accounts
- Paid Time Off (PTO), paid holidays, and paid parental leave
- 403(b) retirement plan with employer match
- Voluntary benefits (supplemental life/AD&D, critical illness, tuition assistance, adoption benefits, backup childcare/eldercare, EAP, and discounts)
Location & Employment Type
- Job location: Chicago, IL (on-site)
- Employment type: Full-time
Equal Opportunity & Hiring Transparency
Careertakes and our client are Equal Opportunity Employers committed to building a diverse and inclusive workforce. We prohibit discrimination or harassment of any kind. To support a fair and efficient hiring process, AI tools may be used to assist with application review or resume screening. These tools do not replace human decision-making. Final hiring decisions are made by people.
If you have questions about how your data is used, please contact us directly.
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