To collect and record preliminary data for clinical research programs. To
recruit and perform follow-up with research participants as protocols outline.
To schedule visits according to research protocols. To assist in coordination
of lab and fieldwork. To maintain familiarity with appropriate Good Clinical
Practice (GCP) guidelines and regulations.
This position also assists with the completion of Case Report Forms (CRF)
according to protocol.Assists with development of protocols and standard
operating procedures (SOPs) for data quality assurance. Performs general
clerical duties (faxing, scanning, routing messages, coordinating the
purchase of study supplies/materials).
May assist in compiling, editing, and proofing written reports for both
internal and external administrative offices.
May perform data analysis using a variety of software packages.
Uses Electronic Data Capture (EDC) systems necessary for operations under
May perform a variety of medical procedures under supervision.
Perform other duties as assigned
Collects, records and analyzes preliminary data for behavioral and clinical
Recruits, schedules, and performs follow-up with research
This position may perform data analysis using a variety of
Knowledge of the principles and procedures of clinical...