Social/Clinical Research Assistant
About The Position
This position will serve as an Associate Clinical Research Coordinator within the Department of Psychiatry working primarily on the Adverse Adolescent Pathways to Substance Use Study ( APSU ) also known as the Pathways to Adolescent Success Study ( PASS ) which is a multidisciplinary, longitudinal research project led by Drs. Aysenil Belger, Diana Fishbein, and Ty Ridenour within the Psychiatry Department focused on examining neurobiological, physiological, and behavioral development in adolescents with symptoms of anxiety. The Associate Clinical Research Coordinator is responsible for the execution of clinical research protocols, including leading efforts in gathering, compiling, and reporting data for a variety of research studies. The Associate Clinical Research Coordinator serves as the primary point of contact for all study protocols and coordination, including recruitment, screening, enrollment and management of study participants, supervision of the execution of study procedures, conducting study visits, and entering, reviewing, and analyzing study data. This position also assists with the preparation and submission of regulatory documents, including Institutional Review Board ( IRB ) modifications, amendments, and adverse event reporting, as well as budget management and purchase reconciliation. Finally, this position is responsible for the training and education of research staff and undergraduate research assistants, the facilitation of team meetings and communication across study domains, and other coordination aspects of a collaborative multidisciplinary clinical research study.
Responsibilities
- Execution of clinical research protocols
- Gathering, compiling, and reporting data for a variety of research studies
- Primary point of contact for all study protocols and coordination, including recruitment, screening, enrollment and management of study participants
- Supervision of the execution of study procedures
- Conducting study visits
- Entering, reviewing, and analyzing study data
- Assists with the preparation and submission of regulatory documents, including Institutional Review Board ( IRB ) modifications, amendments, and adverse event reporting
- Budget management and purchase reconciliation
- Training and education of research staff and undergraduate research assistants
- Facilitation of team meetings and communication across study domains
- Other coordination aspects of a collaborative multidisciplinary clinical research study
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What This Job Offers
Job Type
Full-time
Career Level
Entry Level
Education Level
No Education Listed
