Clinical Research Coordinator 2 - Ophthalmology

About The Department The Office of Clinical Research (OCR) is dedicated to supporting the infrastructure for the management and administration of clinical research at The University of Chicago and individual research programs. Its mission is to catalyze clinical research by providing expertise, resources, infrastructure, and systems that facilitate operations and enable collaboration across the enterprise while promoting compliance and human subject protection. Job Summary The Clinical Research Coordinator 2 – Ophthalmology (CRC2) works under the direction of the Principal Investigator and other study personnel to follow the clinical protocol, perform study‑related tasks, and ensure compliance with federal and institutional regulations. The position is housed within the Clinical Research Incubation Unit and collaborates with investigators in one or more clinical departments. 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 (IRB submissions, educational materials, reports, grant renewal reports, study forms). Act as a liaison with clinical staff, university departments, ancillary departments, and satellite facilities. Maintain knowledge of current protocols and internal SOPs; develop standard work to support efficient workflows. Follow procedures, maintain records, track progress, and respond to data queries in a timely manner. Analyze, facilitate, and participate in daily activities of moderately complex clinical trials, including data management, patient data retrieval, chart preparation, and program audits. Solve straightforward problems related to compliance, financial, and other aspects of a clinical study. Coordinate the collection of analyzable clinical research data and/or samples with a moderate degree of independence, and contribute to problem‑solving on assigned studies and tasks. Perform other related work as needed. Education and Qualifications Education (Minimum) – A college or university degree in a related field. Work Experience (Minimum) – 2–5 years of experience in a related job discipline. Preferred Competencies Strong knowledge of clinical research regulations and best practices. Excellent time management and ability to prioritize work assignments. Ability to read and understand clinical trial protocols. Ability to work collaboratively with professionalism. Strong interpersonal skills. Comfort in clinical settings and patient interaction. Working Conditions Clinical research environment. Benefits Benefits eligible: Yes. The University of Chicago offers a range of benefits, including health, retirement, and paid time off. Posting Statement The University of Chicago is an equal‑opportunity employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national or ethnic origin, age, disability, veteran status, genetic information, or other protected classes under the law. Job seekers requiring reasonable accommodation should contact View phone number on click.appcast.io or submit a request via Applicant Inquiry Form. Compensation and Work Hours Salary: $60,000.00 – $75,000.00. Weekly hours: 40. Exempt under FLSA. Additional Employment Requirements Drug Test Required: Yes Health Screen Required: Yes Motor Vehicle Record Inquiry Required: No #J-18808-Ljbffr