Clinical Research Coordinator
Job description
The ideal candidate will support clinical trial coordination activities across studies. The position will recruit and perform follow-up with research participants according to research protocols. This candidate must maintain familiarity with appropriate Good Clinical Practice (GCP) guidelines and regulations.
Key Duties and Responsibilities
- 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.
- Assists in coordination of lab and fieldwork.
- Prepares for study monitoring visits and correcting findings.
- 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). 6. May perform a variety of medical procedures under supervision.
- 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 supervision.
- Performs other duties as assigned
Annual Salary Range - $41,175 - $66,915
High School diploma or GED required.
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