Clinical Research Professional (I, II or III) Department of Internal Medicine, Division of Pulmonary

University of Cincinnati
Cincinnati, OH

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 53,600 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 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 Department of Internal Medicine is a top-tier department with a world-renowned faculty and staff.

One full-time Clinical Research Professional (CRP) staff position is available in the Division of Pulmonary, Critical Care and Sleep Medicine. This position may be CRP I, CRP II, or CRP III as the level of the position will depend on the candidate's education and experience. Duties can span a broad range of activities or be primarily focused within one or more areas of the clinical research spectrum.

Clinical Research Professional I

Provide technical support and assistance for a designated department, program, or central unit. Duties can span a broad range of activities or be primarily focused within one or more areas of the clinical research spectrum.

Clinical Research Professional II

Plan, evaluate, coordinate and/or manage elements of multiple or complex clinical research projects for a designated department, program, or central unit. Duties can span a broad range of activities or be primarily focused within one or more areas of the clinical research spectrum.

Clinical Research Professional III

Design, evaluate, coordinate and/or manage elements of multiple or complex clinical research projects for a designated department, program, or central unit. Duties can span a broad range of activities or be primarily focused within one or more areas of the clinical research spectrum.

Essential Functions

Clinical Research Professional I
  • Plan and coordinate clinical research projects.
  • Screen patients for admittance in study based on pre-determined criteria.
  • In conjunction with the investigator, document and evaluate adverse events and response to treatment.
  • Coordinate the generation of data for proposals, reports, and manuscripts. Assist in development of reports.
  • Perform routine physical/clinical procedures.
  • Ensure compliance with contract principles, federal regulations, laws and University of Cincinnati (UC)/University of Cincinnati Physicians Company (UCPC) policy and operating procedures.
  • Maintain regulatory documentation. Prepare IRB submissions.
  • Draft subject informed consents and consent comprehension tests. Assist in drafting compliant advertisements.
  • Liaison with medical staff, university departments, ancillary departments, satellite facilities, IRB, and industry contacts.
Clinical Research Professional II
  • Provide direction, instruction and guidance to coordinate research activities, including patient screening and recruitment, enrollment and education. Ensure protocol procedures have been completed adhering to Good Clinical Practice Guidelines as defined by the Federal Drug Administration (FDA) and serve as subject matter expert.
  • Collaborate with care coordinators, social workers, psychologists, physicians and other appropriate treatment team members in diagnostic formulation, treatment direction, and recommendations. Act as a liaison with medical staff, university departments, ancillary departments and/or satellite facilities.
  • Assist with developing and revising policies and procedures for the research team to ensure compliance with the protocol.
  • Serve as a resource within the department for the development of less experienced team members.
  • Contribute to the development of new processes, procedures, tools and training to enhance clinical research activities, compliance, and efficiency.
  • Ensure compliance with contract principles, federal regulations, laws and University of Cincinnati/University of Cincinnati Physicians Company (UCPC) policy and operating procedures.
  • Perform related duties based on departmental need. This job description can be changed at anytime.
Clinical Research Professional III
  • Provide direction, instruction and guidance to coordinate research activities including patient screening and recruitment, enrollment and education. Ensure protocol procedures have been completed adhering to Good Clinical Practice Guidelines as defined by the Federal Drug Administration (FDA) and serve as subject matter expert.
  • Independently coordinate nursing/social work and patient care and/or patient follow-up functions of the clinical study including planning and developing related activities. Provide quality patient care to patients and their families within area of clinical specialty.
  • Collaborate with care coordinators, social workers, psychologists, physicians and other appropriate treatment team members in diagnostic formulation, treatment direction, and recommendations. Act as a liaison with medical staff, university departments, ancillary departments and/or satellite facilities.
  • Initiate and assist with developing and revising policies and procedures for nursing practice.
  • Serve as a peer-mentor within the department, supporting management and in various responsibilities as appropriate including the development of less experienced team members.
  • Contribute to the development of new processes, procedures, tools and training to enhance clinical research activities, compliance, and efficiency.
  • Ensure compliance with contract principles, federal regulations, laws and University of Cincinnati/University of Cincinnati Physicians Company (UCPC) policy and operating procedures.
  • Perform related duties based on departmental need. This job description can be changed at any time.
Required Education

Clinical Research Professional I
  • Bachelor's Degree must be in a related field.
  • Five (5) years of relevant education, experience and/or other specialized training can fulfill minimum education and experience requirements
Clinical Research Professional II
  • Bachelor's Degree must be in a related field.
  • Seven (7) years of relevant education, experience and/or other specialized training can fulfill minimum education and experience requirements
Clinical Research Professional III
  • Bachelor's Degree must be in a related field.
  • Nine (9) years of relevant education, experience and/or other specialized training can fulfill minimum education and experience requirements
Required Experience

Clinical Research Professional I
  • One (1) year of related experience.
Clinical Research Professional II
  • Three (3) years relevant experience
Clinical Research Professional III
  • Five (5) years of relevant experience
Required Trainings/Certificates

Clinical Research Professional III
  • SoCRA/ACRP/RAPS certification
  • For patient facing role, CPR certification
Additional Qualifications Considered

Clinical Research Professional I and II
  • Experience in an academic or clinical setting in the area of clinical specialization.
Clinical Research Professional III
  • Master's Degree
  • Experience in an academic or clinical setting in the area of clinical specialization.
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 security, and work-life balance. (UC Benefits) Eligibility may vary by position and FTE status. Highlights include:

Salary/Hourly Pay Rate Information:

Comprehensive Tuition Remission

UC provides tuition remission for you and your eligible dependents, covering tuition costs for nearly all undergraduate and graduate programs offered by the university.

Robust Retirement Plans

As a UC employee, you won't contribute to Social Security (except Medicare). Instead, you'll choose between state pension plans (OPERS, STRS) or an Alternative Retirement Plan (ARP), with UC contributing 14-18% of your salary based on position.

Real Work-Life Balance

UC prioritizes work-life balance with a generous time-off policy, including:

Vacation and sick time

11 paid holidays and additional end-of-year paid time off (Winter Season Days)

6 weeks of paid parental leave for new parents

Additional Benefits Include:
  • Competitive salary based on experience
  • Comprehensive health coverage (medical, dental, vision, prescription)
  • Flexible spending accounts & wellness programs
  • Professional development & mentorship opportunities
To learn more about why UC is a great place to work, please visit our Careers Page .

UC is an E-Verify employer. If hired into this position, you will be required to provide satisfactory proof of employment eligibility by providing acceptable, original forms of identification for employment verification via the Federal I-9 employment verification process. Click here for a list of acceptable documents.

Important : To apply you must create a profile and submit a complete job application through the UC applicant portal . We are unable to consider "easy apply" applications submitted via other websites. For questions about the UC recruiting process or to request accommodations with the application, please contact UC HR at [email protected] .

Equal Opportunity Employer. Building a workplace where all qualified applicants will receive consideration for employment, including Individuals with Disabilities and Protected Veterans.

REQ: 101992
Posted 2026-04-12

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