Clinical Research Coordinator II — Pediatric Heart Center

10 HOSP Ann & Robert H. Lurie Children's Hospital of Chicago; Chicago (IL); On-site; USD 50,000 - 82,000; Full time

Benefits offered by this job

Medical insurance

Dental insurance

Vision insurance

403(b) retirement plan

Paid time off

Job summary

Ann & Robert H. Lurie Children’s Hospital of Chicago is seeking a Clinical Research Coordinator to coordinate initiation, regulatory approvals, and daily study activities for pediatric trials.

The role requires regulatory expertise, strong data management, and patient-facing communication. You will manage visits, consent processes, and study documentation while collaborating with multi-disciplinary teams in a fast-paced environment.

Qualifications

• Bachelor’s degree and one year of research experience required.
• Knowledge of FDA, HSR and GCP guidelines.
• Proficient organizational and written communication skills.

Responsibilities

• Coordinate initiation and regulatory approvals for clinical studies.
• Maintain study documents and regulatory binders with adherence to protocols.
• Oversee clinic visits, site qualification, initiation, monitoring and close-out visits.
• Collect specimens, document data, and support QA/QC for data accuracy.
• Engage participants, obtain informed consent, coordinate reimbursements and act as patient liaison.
• Manage supplies and equipment inventory, including lab kits and requisitions.
• Track grants and deliverables deadlines; prepare data abstracts and codes for processing.
• Participate in investigator meetings and support ethical conduct of research.

Skills

Regulatory compliance

IRB coordination

Study coordination

Data collection

Communication

Team collaboration

Education

Bachelor’s degree and 1 year research experience

Job description

Ann & Robert H. Lurie Children’s Hospital of Chicago is seeking a Clinical Research Coordinator to coordinate initiation, regulatory approvals, and daily study activities for pediatric trials.

The role requires regulatory expertise, strong data management, and patient-facing communication. You will manage visits, consent processes, and study documentation while collaborating with multi-disciplinary teams in a fast-paced environment.