DescriptionUnder minimal supervision, coordinates the clinical assessments of the study subjects; analyzes and assists in interpreting moderately complex clinical research data. Prepares grant applications and documents and assists in protocol submissions (for e.g., Institutional Review Board, Grants and Contracts Office).
ResponsibilitiesAnalyzes moderately complex clinical research data; Assists in interpreting clinical research data.Coordinates the clinical assessments of the study subjects including but not limited to screening and evaluation of the study subjects.Prepares and ensures grant applications, IRB/GCO documents are submitted.Ensures accurate and complete compilation of subject data through chart reviews.Assists the Principal Investigator and regulatory staff in the preparation of new protocol submissions, protocol amendments, and renewals of ongoing clinical trials.Obtains informed consent und...