Pool Clinical Research Assistant
About The Position
Under the supervision of the Research Coordinators, Clinical Research Supervisors, and Clinical Research Manager, this role assists research personnel with multiple research projects. Responsibilities include pre-screening subjects for eligible studies based on broad eligibility criteria, obtaining informed consent for non-interventional registry, observational, and select minimal risk device studies, and documenting the informed consent process. The role also involves reviewing eligibility criteria with the Principal Investigator and Clinical Research Coordinators/Nurses/LPN, assisting with subject enrollment and randomization, and coordinating research visits. Additionally, the position requires reviewing study-specific lab manuals, obtaining and processing lab specimens as per protocol, performing data entry by transcribing data from source to case report forms (paper or electronic), and redacting source documents as requested. The Clinical Research Assistant serves as a liaison between research staff and departments where research is conducted and performs other assigned duties. Requires basic computer skills and knowledge of Microsoft Office products. Responsible for performing job duties in accordance with the mission, vision, and values of Tampa General Hospital.
Requirements
- Requires basic computer skills and knowledge of Microsoft Office products
- Responsible for performing job duties in accordance with mission, vision and values of Tampa General Hospital
- Bachelor’s degree in field related to science or health care
- Knowledge of medical terminology
Nice To Haves
- Current certification in phlebotomy is preferred
- Knowledge of principles and techniques used in clinical research preferred
Responsibilities
- 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
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What This Job Offers
Job Type
Full-time
Career Level
Entry Level
