General Responsibilities

• 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.

Key Duties & Responsibilities

1. Collects and records preliminary data for clinical research programs. Recruits and performs follow-up with research participants as protocols outline. Schedules visits according to research protocols.
2. Assists in coordination of lab and fieldwork. Prepares for study monitoring visits. Assists with correcting findings.
3. Assists with the completion of Case Report Forms (CRF) according to protocol.
4. Assists with development of protocols and standard operating procedures (SOPs) for data quality assurance.
5. Performs general clerical duties (faxing, scanning, routing messages, coordinating the purchase of study supplies/materials).
6. May perform a variety of medical procedures under supervision.
7. 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.
8. Uses Electronic Data Capture (EDC) systems necessary for operations under supervision.
9. Performs other duties as assigned.