Genetics Clinical Research Coordinator II – Pediatric Trials

Lurie Children's; Chicago (IL); On-site; USD 50,000 - 82,000; Full time

Job summary

Lurie Children's in Chicago is seeking a Clinical Research Coordinator II for Genetics to support translational studies under moderate supervision. The role balances patient-facing tasks with regulatory data management across multiple studies.

Responsibilities include coordinating IRB submissions, site initiation visits, data abstraction, participant consent, and monitoring visits, while maintaining compliance with FDA, GCP, and related guidelines.

Qualifications

• Bachelor’s degree and one year research experience required.
• Proficient organizational skills to manage multiple studies.
• Excellent verbal and written communications.
• Knowledge of FDA, HSR, and GCP Guidelines.
• Strong analytical skills for quantitative and qualitative methods.
• Emerging leadership skills.
• Ability to prioritize tasks and collaborate in a diverse team.

Responsibilities

• Coordinate initiation and regulatory compliance of clinical studies.
• Prepare IRB and sponsor documents and ensure approvals.
• Manage study documents, regulatory binders, source documents.
• Coordinate and oversee study visits, site qualifications, initiation, monitoring, close-out.
• Collect specimens, record data, and ensure protocol compliance.
• Engage participants, conduct informed consent, coordinate reimbursement.
• Oversee supplies and equipment inventory; prep lab kits.
• Track deadlines for grants and deliverables.
• Prepare data for processing and analysis; develop codebooks.
• Participate in investigator meetings and assist with invoicing.

Skills

Organizational skills

Verbal and written communications

FDA knowledge

HSR knowledge

GCP knowledge

Analytical skills

Leadership

Prioritization & problem solving

Fostering inclusive teamwork

Education

Bachelor’s degree or equivalent experience

Job description

Lurie Children's in Chicago is seeking a Clinical Research Coordinator II for Genetics to support translational studies under moderate supervision. The role balances patient-facing tasks with regulatory data management across multiple studies.

Responsibilities include coordinating IRB submissions, site initiation visits, data abstraction, participant consent, and monitoring visits, while maintaining compliance with FDA, GCP, and related guidelines.