Salary
💰 $47,400 - $71,200 per year
About the role
- Implement and manage all phases of study/protocol and ensure compliance with protocol and regulatory requirements
- Establish record-keeping systems and serve as liaison with funding/sponsoring agencies
- Assess participants’ progress, analyze and report adverse events, and make determinations on eligibility and protocol adjustments
- Recruit and enroll study participants, develop informed consent packets, explain study purpose and procedures, obtain consent
- Schedule and facilitate participants’ timely completion of assessments, lab testing, procedures and treatments
- Evaluate and interpret collected clinical data and prepare oral/written reports and analyses
- Analyze images from multiple modalities, retrieve data from intranet repositories, organize and perform preprocessing
- Use existing analytic software (e.g., Freesurfer) to prepare acquired data for analysis and communicate results with researchers
- Collect clinical data and biological samples, perform blood sample acquisition, centrifuge use and shipment of samples
- Perform other duties as assigned
Requirements
- Bachelor’s degree or combination of education and/or experience may substitute for minimum education
- Basic Life Support - American Heart Association or Basic Life Support - American Red Cross (BLS must include skills assessment; online-only BLS insufficient)
- No specific work experience required
- Skills listed: Clinical Research; Clinical Study Protocols; Communication; Computer Literacy; Computer Systems; Interpersonal Communication; Organizing; Research Support; R Statistics
- Driver's license not required