Assists investigators as coordinator of a basic to moderately complex clinical research study to ensure compliance with protocol guidelines and requirements of regulatory agencies
Requirements
- Basic Life Support certification (Online BLS certifications, those without a skills assessment component, are not sufficient to meet the BLS requirements)
- Clinical Research
- Clinical Study Protocols
- Computer Systems
- Office equipment
Responsibilities
- Implements and manages all phases of study/protocol; ensures compliance with protocol guidelines and requirements of regulatory agencies; establishes record-keeping systems; makes assessments and determinations of participants’ progress in the study; analyzes, investigates and reports adverse events
- Recruits and enrolls study participants; makes and/or participates in making determinations of eligibility based on diagnostic criteria and/or observations/analysis in participant interviews
- Ensures timely completion of all protocol requirements (assessment, lab testing, procedures and treatments), to include scheduling and facilitating the patient’s timely completion of protocol requirements
- Evaluates and interprets collected clinical data as appropriate; prepares oral or written presentations or reports and analyses setting forth progress trends and provides recommendations or conclusions of the same
- Collects clinical data under clinical research protocols
- Performs other duties as assigned
- Serves as liaison with funding or sponsoring agency
Other
- Bachelor’s degree or combination of education and/or experience may substitute for minimum education
- No specific work experience is required for this position
- A driver's license is not required for this position
- Up to 22 days of vacation, 10 recognized holidays, and sick time
- Competitive health insurance packages with priority appointments and lower copays/coinsurance
