Clinical Research Professional, UC Cancer Center

at  University of Cincinnati

REQUIRED EDUCATION

• 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

ADDITIONAL QUALIFICATIONS CONSIDERED

• Master’s Degree
• Experience in an academic or clinical setting in the area of clinical specialization.

PHYSICAL REQUIREMENTS/WORK ENVIRONMENT

• Sitting - Continuously

• Follow established CTO workflows and CTO/UC Health standard operating procedures.
• Consent participants to interventional clinical trials. Coordinate screening procedure scheduling and completion.
• Complete eligibility review and verification in conjunction with treating physician/sub-I and CRC team.
• Coordinate treatment appointments/procedures for patients’ duration on study.
• Document study procedures and patient medical history, conmeds, and adverse events in Epic electronic medical record.
• Respond to queries in electronic data capture systems and other online study systems as needed.
• Prepare biospecimen collection supplies,
• Complete ECGs on study-provided ECG machines.
• Coordinate collection, documentation, transportation, and shipment of research biospecimens as needed.
• Document and file deviations through the appropriate regulatory channels as needed.
• Complete financial documentation as needed for research patient visits.
• Prepare and present educational/operational materials.
• Create and maintain positive working relationships with multidisciplinary teams.
• Perform related duties based on departmental/Team needs.