University of Cincinnati-posted 3 months ago
Full-time • Entry Level
Cincinnati, OH
Educational Services

As one of the oldest medical schools in the country, the University of Cincinnati College of Medicine (COM) has a reputation for training best-in-class health care professionals and developing cutting-edge procedures and research that improves the health and clinical care of patients. In partnership with the UC Health academic healthcare system and Cincinnati Children's Hospital Medical Center, College of Medicine's faculty are transforming the world of medicine every day. The University of Cincinnati Cancer Program is recruiting a Clinical Research Professional or Clinical Research Professional II position. This position will support the University's mission and commitment to excellence in our students, faculty, staff and all our activities. Under general supervision, the Clinical Research Professional will provide support and assistance for the University of Cincinnati Cancer Center Clinical Trials Office (CTO). Duties can span a broad range of activities or can be primarily focused within one or more areas of the clinical research spectrum. Please note this is a FULL-TIME, ON-SITE position. NOTE: This position does not qualify for Visa sponsorship.

  • 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.
  • Order, coordinate, and schedule screening and on-study procedures.
  • 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.
  • Utilize 3rd party study systems throughout the patients' participation of study.
  • Prepare biospecimen collection supplies 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.
  • 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.
  • 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.
  • One (1) year of related experience for Clinical Research Professional.
  • Seven (7) years of relevant work experience and/or other specialized training can be used in lieu of education requirement for Clinical Research Professional II.
  • Three (3) years of related experience for Clinical Research Professional II.
  • For patient facing role, CRP certification.
  • Master's degree.
  • Experience in an academic or clinical setting in the area of clinical specialization.
  • Comprehensive Tuition Remission for you and your eligible dependents.
  • Robust Retirement Plans with UC contributing 14-18% of your salary based on position.
  • Generous time-off policy including vacation and sick time, 11 paid holidays, and additional end-of-year paid time off.
  • 6 weeks of paid parental leave for new parents.
  • Competitive salary based on experience.
  • Comprehensive health coverage (medical, dental, vision, prescription).
  • Flexible spending accounts & wellness programs.
  • Professional development & mentorship opportunities.
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