Assists the Clinical Research Manager (CRM) in conducting activities related to human subjects studies, including support of MCGI- Central office managed sites via direct communication with Study participants (primarily via telephone and occasionally face to face in a clinical setting), including obtaining informed consent, Study participant management and retention, data abstraction from medical records, EDC data entry and data review.
January 18, 2020
Performs study specific procedures at protocol directed intervals under the supervision of the PI.
March 31, 2020
Communicates effectively and provides information to a diverse, vulnerable subject population in accordance with institutional policies.
May 04, 2020
Assist the Clinical Research Manager (CRM) and Program Manager (PM) in conducting activities related to billing processing for study-sites, collaborators and consultants.
May 05, 2020
Collecting data through various study paradigms in the lab or in homes (videotaping/audiotaping activities, one-on-one testing of children) and administering phone-based standardized screenings or tests.
May 10, 2020