The organization needs a coordinator to manage and record all phases of a complex clinical research study, ensuring compliance with protocol guidelines and regulatory agencies.
Requirements
- Database Management
- Research Projects
- Spreadsheet Analysis
- Statistical Analysis Software (SAS)
- Clinical Research
- Clinical Study Protocols
Responsibilities
- Confers with PI to assist in developing plans for research projects and discuss the interpretation of results
- Coordinates the development of forms, questionnaires, and the application of research techniques
- Routinely implements and manages all phases of study/protocol
- Evaluates and interprets collected clinical data in conjunction with PI as appropriate
- Prepares oral or written presentations or reports and analyses setting forth progress trends and provides recommendations or conclusions of the same
- Analyzes, investigates, and reports adverse events
- Makes decisions as when to notify physicians of issues, when to stop participant inclusion, and/or to make and/or recommend adjustment of the protocol of particular participants
Other
- Bachelor’s degree or combination of education and/or experience may substitute for minimum education
- Basic Life Support certification must be obtained within one month of hire date
- Clinical Research (2 Years) work experience
- Alternative working schedules
- Exposure to blood-borne training pathogens
- Repetitive wrist, hand, or finger movement
- Occasional lifting (25 - 50 lbs)
