Genetics Clinical Research Coordinator II

luriechildrens; Chicago (IL); On-site; USD 50,000 - 82,000; Full time

Job summary

Ann & Robert H. Lurie Children's Hospital of Chicago is seeking a Clinical Research Coordinator to coordinate and regulate clinical research studies with supervision.

You will manage regulatory documentation, study visits, and patient engagement while ensuring adherence to FDA, HSR, and GCP guidelines. The role requires a Bachelor's degree and at least one year of research experience, with strong organizational and communication skills to support diverse studies and collaboration across

Qualifications

• Bachelor's degree and one year research experience required.
• Proficient organizational skills with ability to manage multiple studies.
• Proficient verbal and written communications skills.
• Proficient knowledge of FDA, HSR, and GCP Guidelines.

Responsibilities

• Coordinates and manages initiation and regulatory compliance of clinical research studies, including preparing documents for IRB and sponsor review, coordinating study conduct across departments, and securing approvals.
• Manages study documents, including regulatory binders, source documents, and correspondence, ensuring adherence to research protocols.
• Oversees all aspects of clinical research visits, including arranging visits, site qualifications, initiation, monitoring, and close-out visits.
• Collects specimens, records data on source documents and electronic systems, and assists with QA/QC procedures to ensure data accuracy and protocol compliance.
• Manages participant engagement by identifying eligible subjects, conducting informed consent, coordinating reimbursement, and serving as the primary patient liaison.

Skills

Regulatory compliance

Data management

Verbal and written communications

Organizational skills

Education

Bachelor's degree

Job description

Ann & Robert H. Lurie Children's Hospital of Chicago is seeking a Clinical Research Coordinator to coordinate and regulate clinical research studies with supervision.

You will manage regulatory documentation, study visits, and patient engagement while ensuring adherence to FDA, HSR, and GCP guidelines. The role requires a Bachelor's degree and at least one year of research experience, with strong organizational and communication skills to support diverse studies and collaboration across