Pediatric Clinical Research Coordinator II – Study Ops

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, dental and vision insurance

403(b) with 5% employer match

Paid Time Off and Holidays

Job summary

Ann & Robert H. Lurie Children’s Hospital of Chicago is seeking a Research Coordinator to coordinate IRB submissions, regulatory compliance, and study conduct across departments. The role balances patient-facing duties with administrative data tasks within pediatric clinical research.

The position requires a Bachelor's degree plus one year of research experience, strong organizational and communication skills, and knowledge of FDA, HSR and GCP guidelines. Competitive benefits accompany the role.

Qualifications

• Bachelor's degree and one year of research experience required, education may substitute for experience.
• Proficient organizational skills with ability to manage multiple studies.
• Proficient verbal and written communications skills.
• Knowledge of FDA, HSR, and GCP Guidelines.
• Proficient analytical skills for research methods and data handling.

Responsibilities

• Coordinate initiation and regulatory compliance of clinical studies, preparing documents for IRB and sponsor review.
• Manage study documents, regulatory binders, source documents and communications.
• Coordinate and oversee clinical research visits, site qualifications, initiation, monitoring and close-out visits.
• Collect specimens, record data, perform QA/QC to ensure data accuracy and protocol compliance.
• Engage participants, obtain informed consent, coordinate reimbursements and serve as patient liaison.

Skills

Research coordination

Data management

Regulatory compliance

Communication skills

Team collaboration

Education

Bachelor's degree in a related field

Job description

Ann & Robert H. Lurie Children’s Hospital of Chicago is seeking a Research Coordinator to coordinate IRB submissions, regulatory compliance, and study conduct across departments. The role balances patient-facing duties with administrative data tasks within pediatric clinical research.

The position requires a Bachelor's degree plus one year of research experience, strong organizational and communication skills, and knowledge of FDA, HSR and GCP guidelines. Competitive benefits accompany the role.