Clinical Research Coordinator 2

About the department

The Office of Clinical Research (OCR) is the nucleus of the clinical research enterprise, providing services, training, tools, and compliance oversight to support the conduct of clinical research across the Biological Sciences Division and University of Chicago Medicine human subject research portfolio. The mission of the Office of Clinical Research is to catalyze clinical research by providing expertise, resources, infrastructure, and systems that facilitate clinical research operations and enable collaboration across the enterprise while promoting compliance and human subject protection on behalf of our diverse community of patients and volunteers.

Responsibilities

• Participate in the coordination and conduct of complex clinical research studies and ensure compliance with federal and institutional regulations.
• Prepare, submit, and assist Investigators with multiple levels of research documentation (i.e. IRB submissions, educational materials, reports, grant renewal reports, and study forms).
• Maintain working knowledge of current protocols, and internal SOPs.
• Develop standard work to support efficient workflows.
• Be accountable for high standards of clinical research practice and assist in the development of accountability in others.
• Follow procedures, maintain records, track progress, and respond to data queries in a timely manner.
• Solve a range of straightforward problems relating to the administration of the compliance, financial, and other related aspects of a clinical study.
• Support drafting and review of peer reviewed study publications under supervision of study PI.
• Accountable for all tasks in moderately complex clinical studies.
• Affords assistance with various professional, organizational, and operational tasks under moderate supervision.
• Facilitates and participates in the daily activities of moderately complex clinical studies and performs various activities including patient data retrieval, documenting clinical research records, and participating in program audits.
• Uses knowledge of clinical studies to coordinate the collection of analyzable clinical research data and/or samples with a limited to moderate degree of independence.
• Contributes to the problem solving on assigned clinical research studies and tasks.
• Performs other related work as needed.

Qualifications

• Education: Minimum requirements include a college or university degree in related field.
• Experience: Relevant research experience. Experience coordinating clinical trials or previous experience coordinating complex clinical trials. Knowledge of medical terminology/environment.
• Certifications: Preferred qualifications include a bachelor's degree.

Benefits

• Benefits Eligible: Yes
• Pay Rate Type: Salary
• Pay Range: $60,000.00 - $75,000.00