
Clinical Research Professional / Clinical Research Professional II, COM, UC Cancer Center
- Cincinnati, OH
- Permanent
- Full-time
- 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. This includes 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, central labs, ECGs, ECHOs, CT, PET, and/or MRI scans, physical exams, pulmonary function tests, cardiac stress tests, biopsies, infusions.
- Complete eligibility review and verification in conjunction with treating physician/sub-I and CRC team.
- Interview patients for baseline and ongoing changes in medical history, concomitant medications, and adverse events, and document within the EPIC electronic medical record.
- Utilize 3rd party study systems throughout the patients’ participation of study, uses include but are not limited to, randomization, registration, dose/drug assignment, uploading of source material, download of specialty reports, data entry.
- Prepare biospecimen collection supplies, including hand off instructions for the clinical nurse(s) or phlebotomist(s), and ensure processing laboratory has accurate processing and shipment manuals and supplies.
- Complete ECGs on study-provided ECG machines when due.
- Coordinate collection, transportation, and shipment of research biospecimens as needed. Process and ship research biospecimens as needed.
- Document and file deviations through the appropriate regulatory channels as needed.
- Complete financial documentation as needed for research patient visits.
- Maintain/Update patients’ status and visit completions in the Clinical Trial Management System.
- Prepare and present educational/operational materials to research and clinical teams on newly opened clinical trials (Implementation meetings).
- Create and maintain positive working relationships with multidisciplinary teams.
- Perform related duties based on departmental/Team needs.
Bachelor’s Degree must be in a related field.
Five (5) years of relevant work experience and/or other specialized training can be used in lieu of education requirement.
Required Experience
One (1) year of related experience.-OR-Clinical Research Professional IIRequired Education
Bachelor’s Degree must be in a related field.
Seven (7) years of relevant work experience and /or other specialized training can be used in lieu of education requirement.
Required Experience
Three (3) years of related experience.Required Trainings/CertificationsFor patient facing role, CRP certification.Additional Qualifications Considered
- Master’s degree.
- Experience in an academic or clinical setting in the area of clinical specialization.
- Office environment/no specific unusual physical or environmental demands.
- Competitive salary based on experience
- Comprehensive health coverage (medical, dental, vision, prescription)
- Flexible spending accounts & wellness programs
- Professional development & mentorship opportunities