CLINICAL RESEARCH COORD B
Duties: With minimal supervision, the clinical research coordinator (CRC) B will participate in the coordination of Phase I-IV breast oncology trials being conducted through the Abramson Cancer Center (ACC) Clinical Research Unit (CRU), Breast Cancer Research Program. The CRC B will be responsible for initiating and conducting participant screening, recruitment, enrollment, study specimen collection, and follow-up for their assigned trials. The CRC B will be responsible for coordinating and scheduling all research required procedures and biospecimen collection from study participants. The CRC B will work closely with the clinical team and study participants to ensure that all study tests and procedures are scheduled and carried out according to protocol requirements. The CRC B will organize, maintain, and keep up-to-date all required research documentation - to include but not limited to source documentation, case report forms, and research charts. The CRC B will collect, review and report study data by completing case report forms and resolving data queries. The CRC B will be responsible for the abstraction of medical record information from subject's electronic medical records, interviews and/or questionnaires for entry into the research databases - including but not limited to RedCap, CTMS, Oracle, etc. The CRC B will be responsible for performing quality assurance checks in order to ensure all data required for reporting, monitoring visits, etc is accurate and up-to-date. The CRC B will schedule and participate in site initiation visits, monitoring visits, close-out visits, and study audits; and will assist the project manager and principal investigator (PI) in the preparation for such visits. The CRC B will track the progress of all newly and previously enrolled study participants, and distribute weekly updates to the investigators and clinical team. The CRC B will participate in study team and disease site group meetings and ongoing protocol training compliance meetings. Finally, the CRC B will also assist in other ongoing research efforts and CRU Breast program related projects as they arise.
Qualifications: Bachelor's degree in scientific or related field and 2-4 years of clinical research experience or an equivalent combination of education and experience required. Effective problem solving abilities; effective communication and writing skills; strong organizational and time management skills; flexible and able to multi-task; demonstrated ability to work as part of a team, as well as independently; knowledge of IRB and human research protection regulations.
Reference Number: 40-28832
Salary Grade: 026
Employment Type: Exempt
Org: CC-Cancer Center
Job Family: I-Technical/Professional Research