Clinical Research Assistant- Radiology
About The Position
We are seeking a full-time Research Assistant to assist with our families. This individual will work closely with our imaging technicians, principal investigators, psychologists, research coordinators, and other research assistants in recruiting families to our studies and with the acquisition of brain imaging data (EEG, MEG, and MRI). The Research Assistant will recruit and consent families for entry into the study. They will also enter data into study REDCap databases, manage data flow, and ensure databases and paperwork are maintained. They will have regular contact with clinical and typically developing populations and their families. Prior experience with some or all of these duties is a plus but is not necessary; training will be provided. Successful applicants will be highly self-motivated and fast learners who enjoy working in bustling research and clinical environments. This position offers valuable clinical research experiences in preparation for applying to graduate school. For this position, we will need the person to be somewhat flexible with regard to their time. Some weeks we may need this person to work later in the evening, while other weeks may require 8am to 4pm.
Requirements
- High School Diploma / GED Required
- Previous relevant clinical research experience Required
- Familiarity with IRB and human subject protection.
Nice To Haves
- Bachelor's Degree Preferred
- At least one (1) year of relevant clinical research experience Preferred
Responsibilities
- Patient/research participant scheduling
- Patient/Research Participant screening for inclusion/exclusion criteria or case history
- Data collection
- Data entry
- Data management
- Laboratory sample processing
- Clinical research study procedures or questionnaire administration
- Organization of research records and/or other study related documentation
- Adhere to IRB approved protocols and compliance with HIPAA and handling confidential materials
- Comply with Institutional policies, SOPs and guidelines
- Comply with federal, state, and sponsor policies
- Consent subjects, with appropriate authorization and training
- Document and report adverse events
- Maintain study source documents
- Complete case report forms (paper and electronic data capture)
- Assist with IRB/regulatory submissions
- Complete case report forms or other study documentation (paper and electronic data capture)
- Follow-up care
- Order materials/supplies
- Schedule research meetings
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What This Job Offers
Job Type
Full-time
Career Level
Entry Level
Education Level
High school or GED
