Job description

Duties: Review protocols and give feedback on feasibility and execution of potential clinical trials; recruit, review informed consents, check eligibility, and enroll subjects into clinical trials according to protocol; check lab results and grade according to CTCAE; update adverse experience checklists for each subject in research; coordinate scheduling of subjects in research within appropriate time limits; supervise clinical research coordinators in the appropriate and timely reporting of AEs, case report forms and protocol related procedures; collaborate with other departments and team members involved in research; complete evaluations, data collection, assessments, source documents, adverse experience reports, and case report forms within appropriated time limits; perform necessary screening and routine evaluations in clinical trials including phlebotomy, physical assessments, EKGs, and intravenous infusions; provide support, health education, and follow up for subjects involved in research and help medically managed patients; attend conferences and classes to stay personally and professionally updated on health care information. Obtain 30 CEUs every two years for RN licensure.

Qualifications: The minimum of an RN and 4 to 5 years of experience or an equivalent combination of education and experience is required. Bachelor's or Master's degree preferred. Experience in clinical trials/clinical research preferred. Effective problem solving abilities, effective communication and writing skills, ability to multi-task, and demonstrated ability to work as part of a team as well as independently are preferred. Knowledge of IRB and human research protection regulations preferred.

Reference Number: 40-30557

Salary Grade: 028

Employment Type: Exempt

Org: OT-Otorhinolaryngology

Special Requirements:

Job Family: J-Technical/Professional Medicine/Health




Diversity Profile: University



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Job No:
Posted: 12/6/2018
Application Due: 1/10/2019
Work Type: