The Visiting Research Associate II will conduct participant screenings and obtain informed consent, according to established research protocols. The position will also implement data collection protocols and procedures for physical measurements and web-based data collection, primarily via REDCap. The Viisiting Research Associate II will assist with recruitment of participants across multiple avenues, including direct and indirect, virtual and in-person methods.
Duties & Responsibilities Perform surveys, interviews, observations or uses other methods according to established research protocols. Collect, process and analyze data. Summarize research and test results.
May assist with study protocol development. Coordinate the ordering, inventory and maintenance of equipment, instruments and data collection and analysis tools. Prepare and contributes statistical data and pertinent information for papers, grants and other documents.
Complete required documentation for regulatory agencies. Perform other related duties and participate in special projects as assigned. DEPARTMENT SPECIFIC DUTIES Conduct participant screenings and obtain informed consent, according to established research protocols.
Implement data collection protocols and procedures for physical measurements and web-based data collection, primarily via REDCap. Including collection and monitoring of physical function mobility assessments. Assist with recruitment of participants across multiple avenues, including direct and indirect, virtual and in-person methods.
Assist in developing study forms, measures, protocols, and training guides. May assist with presentation of weekly updates on participant recruitment, retention, engagement, and randomization/enrollment. Support IRB submissions and maintenance of UIC IRB approvals.
Assist in training new staff in recruiting, tracking, and assessing participants for enrollment and follow-up; making contact with legal guardians (for youth); maintaining communication with participants across various media (telephone, email, texts), including intervention engagement; and implementing clinical incident procedures and submitting reports as necessary. Perform other related duties and participate in special projects as assigned.
Assist with participant retention activities, including reminder calls, check-ins, transportation coordination, and other strategies to support continued participation in study assessments and intervention sessions. Assist with processing participant incentives and transportation reimbursement, etc. Perform other related duties and participate in special projects as assigned.
Perform other related duties and participate in special projects as assigned.