Senior Clinical Research Coordinator – End-to-End Lead

Lurie Children's Hospital; Chicago (IL); On-site; USD 59,000 - 97,000; Full time

Benefits offered by this job

Medical, dental and vision insurance

403(b) with a 5% employer match

Paid Time Off

Job summary

Lurie Children’s Hospital in Chicago is seeking a Clinical Research Coordinator to coordinate all clinical research activities across study start-up, monitoring, and close-out, while ensuring regulatory compliance and ethical conduct. The role includes managing regulatory documents, data entry, and budget considerations, with primary focus on patient engagement and sponsor communications.

The position requires a Bachelor’s degree and 2+ years of research experience, strong knowledge of FDA, HSR,

Qualifications

• Bachelor’s degree and two or more years research experience required.
• Strong knowledge of FDA, HSR, and GCP Guidelines.
• Excellent organizational and communication skills; ability to mentor team members.

Responsibilities

• Coordinate all clinical research activities including start-up, site qualification, initiation, monitoring and close-out visits.
• Oversee site visits, address sponsor queries, and ensure adherence to study protocols and regulatory requirements.
• Manage regulatory documentation and submissions (FDA, IRB/ethics, registrations on clinicaltrials.gov) and develop SOPs.
• Promote ethical conduct and integrity in study conduct and data handling.
• Coordinate logistics, prepare lab kits, manage regulatory binders and source documents, and track grants and deliverables.
• Identify and recruit eligible subjects, conduct informed consent/assent, coordinate reimbursements, and serve as main study contact.

Skills

Regulatory compliance

Data management

Study coordination

Communication

Leadership

Education

Bachelor’s degree in a related field

Job description

Lurie Children’s Hospital in Chicago is seeking a Clinical Research Coordinator to coordinate all clinical research activities across study start-up, monitoring, and close-out, while ensuring regulatory compliance and ethical conduct. The role includes managing regulatory documents, data entry, and budget considerations, with primary focus on patient engagement and sponsor communications.

The position requires a Bachelor’s degree and 2+ years of research experience, strong knowledge of FDA, HSR,