Clinical Research Professional / CRP II / CRP III, College of Medicine, UC Cancer Center, Regulatory

Current UC employees must apply internally via SuccessFactors 

 

Next Lives at the University of Cincinnati 

Founded in 1819, the University of Cincinnati ranks among the nation’s best urban public research universities. Home to more than 53,000 students, 12,000 faculty and staff, and over 350,000 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 $88.8 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 at uc.edu. 

 

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.   

Job Overview

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 Center is looking to fill one (1) Regulatory Affairs Clinical Research Professional, Clinical Research Professional II, or Clinical Research Professional III role. This position will be responsible for overseeing a study from initial interest through opening to accrual at UC.

 

NOTE: This position does not qualify for Visa sponsorship.

Essential Functions

• Work to support feasibility and scientific review processes.
• Completing initial IRB submission.
• Assist in preparation of site adapted ICF according to local requirements.
• Collecting and completing essential regulatory documentation for start-up.
• Coordinating contract and budget submissions.
• Providing ongoing status reports about studies in start-up process.
• Interacting daily with sponsors, CROs, and internal UC staff.
• Related, other duties as assigned.

Minimum Requirements

Clinical Research Professional:

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.

-OR-

Clinical Research Professional II:

Required 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.

- OR-

Clinical Research Professional III:

Required Education
Bachelor’s Degree.
Nine (9) years of relevant education, experience and/or other specialized training can fulfill minimum education and experience requirements.
Required Trainings/Certifications
SoCRA/ACRP/RAPS certification.
Required Experience
Five (5) years of related experience.

Physical Requirements/Work Environment

• Office environment/no specific unusual physical or environmental demands.

Compensation and Benefits

UC offers an exceptional benefits package designed to support your well-being, financial sec