OPS - Clinical Research Assistant

Associate's degree in appropriate area and one year or relevant experience; or an equivalent combination of education and experience

Coordinate and manage assigned research studies. Activities include the following: screen, recruit and consent eligible participants, work with clinical team to collect and enter patient data, perform chart review, attend relevant trainings and meetings, and coordinate communication for the study team. Additional activities include managing data and performing quality assurance checks for the Informed Consent and other relevant study documents.

Work with clinical research study team to prepare for study visits to include preparing study questionnaires, scheduling patient visits and coordinating communication. Label and process clinical samples as needed. Manage data queries, assist with projects to support related clinical initiatives, maintain accurate records within OnCore. Run reports as requested. Maintain up-to-date study records

$20.00 hourly

Associate's degree in appropriate area and one year or relevant experience; or an equivalent combination of education and experience

Experience working in clinical setting preferred.

Experience working within UF"s clinical research system preferred

Multi-media capabilities strongly preferred, proficiency with Microsoft Office 

Application must be submitted by 11:55 p.m. (ET) of the posting end date.

Please attach CV/resume and cover letter, 

We are hiring two .50 FTE positions from this posting.