Clinical Research Coordinator, Intervention Study (Psychiatry) (Job ID #149428)

Job Responsibilities (Essential Duties) 

Conduct structured clinical interviews and assessments of patients in research protocols.

Assist in the establishment and coordination of clinical research protocols and organizational structure.

Coordinate the activation and maintenance of clinical protocols, including review and completion of submissions, amendments, and adverse event reports as required by the UIC Institutional Review Board (IRB) and grant sponsors.

Review laboratory and clinic procedures and evaluations regularly to ensure protocol compliance. 

Act as a liaison between staff and the UIC IRB office, grant sponsors, and regulatory agencies to ensure priorities are clearly communicated and resources are allocated appropriately across ongoing projects.

Assist the Primary Investigator in the identification, recruitment, and enrollment of patients to meet clinical research protocol requirements.

Execute informed consent process and monitor patient status; enroll patients into research studies, explain the studies to the patients and obtain/document proper informed consent.

Ensure that patient enrollment and research activities comply with the established protocols, regulatory and monitoring agency standards, and grant sponsor guidelines.

Assist investigator in organizing study data for grant progress reports, analysis for meeting presentations and publications.

Performs other related duties and participate in special projects as assigned.