Pool Clinical Research Assistant

Assists research personnel with multiple research projects

Pre-screens for eligible subjects for assigned studies based on written, broad eligibility criteria.

Obtains consent from patients who will participate in non-interventional registry and observational studies, as well as some select, minimal risk device studies.

Documents the informed consent process.

Reviews eligibility criteria with the Principal Investigator and Clinical Research Coordinators/Nurses/LPN.

Assists with enrollment and randomization of subjects.

Assists with the coordination of research visits.

Reviews study specific lab manuals, obtains and processes lab specimens as required by the specified research protocol.

Performs data entry by transcribing data from the source to the case report form (paper or electronic) and redacts source documents as requested.

Serves as a liaison between research staff and the departments in which research is conducted.

Performs other duties as assigned