CLINICAL RESEARCH COORD A
Duties: Clinical Research Coordinator A will monitor and coordinate Phase I-IV clinical trials/ clinical research drug studies of depression and bipolar disorder. Duties will include:(1)Recruitment: Developing advertisements; recruit, screen and enroll potential study patients as specified per protocol (2)Study Oversight: attend Investigator Initiation meetings; coordinate patient study visits; prepare study material and medication; maintain patient records; implement and ensure protocol adherence to established guidelines; ensure drug accountability; prepare and submit study-related IRB documentation (initial submissions, amendments, continuations) ; resolve data queries with sponsors and CROs; document and report adverse events; participate in the conduct of audits by study sponsors and CROs, as required; manage clinic for patients in various treatment protocols; and assist with taking vitals, drawing blood, preparing blood work, and performing EKGs.
Position is contingent on continued funding.
Qualifications: A Bachelor's Degree and 1 year to 3 years of experience or equivalent combination of education and experience required.
Reference Number: 40-26594
Salary Grade: 025
Employment Type: Exempt
Org: PS-Affective Disorders Program
Special Requirements: Background check required after a conditional job offer is made. Consideration of the background check will be tailored to the requirements of the job.
Job Family: I-Technical/Professional Research