
Clinical Research Professional, Department of Internal Medicine, Division of Infectious Diseases
- Cincinnati, OH
- Permanent
- Full-time
- 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.
- Coordinate nursing and patient care as applicable to research studies. Actively participate in patient care and/or patient follow-up.
- 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.
- Ensure research staff complete all requisite training.
- May serve as a resource person or act as a consultant within area of clinical expertise.
- Plans, implements and coordinates all aspects of assigned studies, including creation of study specific source documentation.
- Conducts study participant assessments for patients including Informed Consent and study eligibility, and collection of all necessary documentation.
- Draws and/or coordinates required study labs following Good Clinical Practice and documenting appropriately.
- Follows large caseload of study participants from study screening through end-of-study evaluations, including all necessary source documentation and data collection/entry.
- Identifies, collects and analyzes data that serve as a basis for outcome measurement of assigned clinical research studies.
- Assist in establishing standard operating procedures for continuous review and development of quality improvement plans for our research operation.
- Attends meetings as assigned.
- Perform related duties based on research program need and as delegated/assigned by the Principal Investigator. This job description can be changed at any time.
- 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.
- For nursing focused role, BSN in the area of clinical specialization, and RN License in State of Ohio.
- For social work focused role, licensure in the area of clinical specialization.
- One (1) year of related experience.
- For nursing focused roles, appropriate clinical procedural experience.
- Experience in an academic or clinical setting in the area of clinical specialization.
- Excellent oral and written communication skills.
- Meticulous source documentation skills.
- Proficiency in various computer and software applications is ideal.
- Prior experience with REDCap is ideal.
- Infectious Diseases experience is ideal.
- Office environment/no specific unusual physical or environmental demands.
- Competitive salary based on experience
- Comprehensive health coverage (medical, dental, vision, prescription)
- Flexible spending accounts & wellness programs
- Professional development & mentorship opportunities