The Department of Neurology at The University of Chicago Medical Center is seeking a Clinical Research Coordinator II to support, facilitate, and coordinate daily clinical trial activities, playing a critical role in the conduct of studies.
Requirements
- knowledge and skills developed through 2-5 years of work experience in a related job discipline.
- Clinical research experience or relevant experience.
- Experience coordinating multiple studies (e.g., investigator initiated, industry sponsored, multi-site trials).
- Ability to comprehend technical documents.
- Working knowledge of Good Clinical Practices (GCP).
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.
- Maintains accurate and complete records which may include, but are not limited to, signed informed consent, relevant IRB approvals, source documentation, Case Report Forms (CRF's), drug dispensing logs, and study related communication.
Other
- Minimum requirements include a college or university degree in related field.
- Strong communication skills (verbal and written).
- Excellent interpersonal skills.
- Adaptability to changing working situations and work assignments.
- Ability to develop and manage interpersonal relationships.
