About this role
About the Role The University of Cincinnati Cancer Program is recruiting a Clinical Research Professional or Clinical Research Professional II to support the Cancer Center Clinical Trials Office (CTO). Working under general supervision, the role provides support and assistance across the clinical research spectrum to advance the university’s cancer research mission and its collaboration with UC Health and Cincinnati Children’s Hospital Medical Center. What You'll Do
- Complete training and follow established CTO workflows and CTO/UC Health standard operating procedures.
- In conjunction with the investigator, consent participants to interventional clinical trials, including providing education of clinical trial design (phases 1-4), explaining primary research aims, reviewing screening procedures, dosing schedule, potential side effects (some of which are unknown), anticipated benefits of trial participation, costs/coverage of treatment, and compensation for participating (if any).
- Order, coordinate, and schedule screening and on-study procedures, including but not limited to local labs. What We're Looking For
- Ability to complete required training and adhere to CTO workflows and UC Health SOPs.
- Experience or ability to consent participants to interventional clinical trials and communicate clinical trial concepts to participants.
- Knowledge of clinical trial design (phases 1-4), screening procedures, dosing schedules, potential side effects, benefits, and cost/coverage considerations.
- Strong organizational skills to order, coordinate, and schedule screening and on-study procedures in collaboration with investigators.