The job is looking to solve the business problem of managing and coordinating complex clinical research studies to ensure compliance with protocol guidelines and requirements of regulatory agencies.
Requirements
- Clinical Research
- Clinical Study Protocols
- Database Management
- Research Projects
- Spreadsheet Analysis
- Statistical Analysis Software (SAS)
- Basic Life Support certification
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
- Resolves IRB/protocol management issues and recommends corrective action as appropriate
- Serves as liaison with funding or sponsoring agency
Other
- Bachelor’s degree or combination of education and/or experience may substitute for minimum education
- Clinical Research (2 Years) work experience
- Basic Life Support certification must be obtained within one month of hire date
- Alternative working schedules
- Exposure to blood-borne training pathogens
- Repetitive wrist, hand, or finger movement
- Occasional lifting (25 - 50 lbs)
