Responsible for scheduling and confirming visits within assigned time frame and ensuring participants are prepared for the visits. Educates participants about the research protocol; informs participants of their rights and responsibilities, and obtains informed consent. Conducts telephone or in-person interviews to complete questionnaires.

This Research technician will be responsible for processing biospecimens, including blood and urine samples for storage. The Research Study technician will assist in the maintenance of study documents, participate in weekly study meetings, and enter clinical data into the established data management system (REDCap).

Makes notations of participant contact information updates. Gathers data & information from various collaborating sites, ensuring all forms are complete. Tracks information; enters into database. Begins to interpret results. Follows established procedures, making judgmental calls regarding reliability and accuracy of results, repeating procedures when needed.

Informs staff at health centers of missing and required information to ensure all forms meet agency compliance. Provides general clerical support, such as handling forms, making reminder phone calls, preparing study materials, sending mail-outs, filing, making appointments, photocopying, faxing, running reports, etc.

Adheres to legal, professional and ethical codes with respect to confidentiality and privacy. Responsible for obtaining and maintaining all study certifications, including Human Subjects Certification.

Participates in special projects and other duties as needed.