Clinical Research Professional​/Clinical Research Professional II, UC Cancer Center

Current UC employees must apply internally via Success Factors.

Founded in 1819, the University of Cincinnati ranks among the nation’s best urban public research universities. Home to more than 53,600 students, 12,000 faculty and staff, and over 360,000 living alumni, UC, a Carnegie 1 institution, combines research prowess with a physical setting. The New York Times has called “the most ambitious campus design program in the country.” UC's momentum has never been stronger as the anchor of the Cincinnati Innovation District, the oldest cooperative education (co-op) program in the country with students earning $94 million annually through paid experiences, an academic health system, and as a member of the Big 12 Conference.

The university contributes $10.6 billion in economic impact to the city and $22.7 billion to the state of Ohio. At UC, next is all of us. Learn more . UC is a mission-driven organization where we are committed to student success and positively transforming the community through scholarship and service. We thrive on innovation, making an impact, and fostering an environment where staff and faculty are key contributors to UC’s success.

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 looking to fill a patient‑facing position as either a Clinical Research Professional or Clinical Research Professional II. This position will support the University’s mission and commitment to excellence in our students, faculty, staff and all our activities. Please note this is a FULL‑TIME, ON‑SITE position, with incidental work from home opportunities.

• Follow established CTO workflows and CTO/UC Health standard operating procedures.
• Proactively review and locate source documentation for all study procedures.
• Accurately enter data from source documentation into electronic data capture (EDC) systems within 5 days of the patient visit.
• Proactively seek to promptly resolve outstanding data queries and any issues through collaboration with clinical research coordinators (CRCs).
• Maintain and use organizational systems to avoid delinquent data entry.
• Review all data entered into EDCs and subject charts to identify and help resolve any general quality issues.
• Conduct study participant follow-up as required per protocol.
• Communicate and collaborate within assigned research team and with principal investigators in a professional, helpful, and service-oriented manner.
• Act as the primary point of contact for monitoring visits.
• Adhere to all UCCC CTO work instructions, SOPs, and study specific time frames.
• Be able to independently maintain and meet form & database development milestones.
• Maintain/update patients’ status in the Clinical Trial Management System.
• Maintain Team’s biospecimen collection kit inventory, re‑ordering supplies as needed.

Clinical Research Professional:

• 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.
• One (1) year of related experience.

Clinical Research Professional II

• 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.
• Three (3) years of related experience.

• Prior experience in clinical research coordination or clinical research data management, and Signal Path, Complion, Red Cap, Inform, Medidata RAVE, etc. systems is ideal.
• Highly comfortable with computer‑based and online systems.
• Must be able to interact and communicate with clinical research staff, PIs, and industry sponsors…