Clinical Research Coordinator: Start-Up, Data & Regulatory

luriechildrens; Chicago (IL); On-site; USD 46,000 - 76,000; Full time

Benefits offered by this job

Medical, dental and vision insurance

Employer paid group life and/or long‑/

Employer contribution toward Health-S<

Flexible Spending Accounts

Paid Time Off

Parental Leave

403(b) with 5% employer match

Voluntary benefits program

Job summary

Lurie Children's Hospital of Chicago is seeking a Clinical Research Support professional to assist investigators and study teams in implementing and coordinating clinical research activities. Under supervision, you will balance patient-facing tasks with administrative data work across programs.

Responsibilities include study start-up, regulatory document maintenance, protocol preparation, and patient coordination.

Qualifications

• Bachelor's degree required or equivalent combination of education and experience.
• Good organizational skills and communication abilities.
• Some knowledge of FDA, HSR, and GCP guidelines.
• Proficient analytical skills and adaptability to various systems.

Responsibilities

• Assist with study start-up and regulatory document maintenance (regulatory binders, source documents, correspondence).
• Prepare protocols, informed consents, amendments for IRB/sponsor reviews.
• Assist clinical research staff in implementing studies and recruiting eligible subjects.

Skills

Organizational skills

Verbal and written communication

FDA knowledge

GCP knowledge

Analytical skills

Education

Bachelor's degree

Job description

Lurie Children's Hospital of Chicago is seeking a Clinical Research Support professional to assist investigators and study teams in implementing and coordinating clinical research activities. Under supervision, you will balance patient-facing tasks with administrative data work across programs.

Responsibilities include study start-up, regulatory document maintenance, protocol preparation, and patient coordination.