The University of Chicago Medical Center's Department of Neurology is seeking a Clinical Research Coordinator II to support, facilitate, and coordinate clinical trial activities, ensuring the conduct of studies and compliance with federal regulations and institutional policies.
Requirements
- Knowledge and skills developed through 2-5 years of work experience in a related job discipline.
- Working knowledge of Good Clinical Practices (GCP).
- Ability to comprehend technical documents.
- Experience coordinating multiple studies (e.g., investigator initiated, industry sponsored, multi-site trials).
- Clinical research experience or relevant experience.
- Ability to develop and manage interpersonal relationships.
- Ability to exercise absolute discretion regarding confidential matters.
Responsibilities
- Manages all aspects of conducting clinical trials including screening, enrollment, subject follow-up, completion of case report forms, and adverse event reports.
- Coordinates the conduct of the study from startup through closeout including recruitment and screening of study subjects, obtaining informed consent, collecting research data, and ensuring protocol adherence and data integrity.
- Recruits and interviews potential study patients with guidance from PI and other clinical research staff.
- Obtains informed consent.
- Plans and coordinates patient schedule for study procedures, return visits, and study treatment schedules.
- Performs assessments at visits and monitors for adverse events.
- Organizes and attends site visits from sponsors and other relevant study meetings.
Other
- Minimum requirements include a college or university degree in related field.
- Minimum requirements include knowledge and skills developed through 2-5 years of work experience in a related job discipline.
- Strong communication skills (verbal and written).
- Excellent interpersonal skills.
- Adaptability to changing working situations and work assignments.
- Ability to follow written and/or verbal instructions.
