CLINICAL RESEARCH COORD A
Duties: Clinical Research Coordinator A will monitor and coordinate Phase I-IV clinical trials and grant funded studies of mindfulness meditation for stress. Duties will include:(1)Recruitment: Developing advertisements; recruit, screen and enroll potential study patients as specified per protocol (2)Study Oversight: attend study startup meetings; coordinate patient study visits; prepare study material and/or medication; maintain patient records; implement and ensure protocol adherence to established guidelines; ensure drug accountability; prepare study-related IRB documentation (initial submissions, amendments, continuations) ; resolve data queries; document and report adverse events; participate in the conduct of audits by study sponsors and OHR, as required; manage clinic for patients in various treatment protocols; and assist with taking blood pressure, weight and height, drawing blood, preparing blood work, and performing EKGs and other measures of cardiac functioning as needed.
Position is contingent on continued funding.
Qualifications: A Bachelor's Degree and 1 to 3 years of experience or equivalent combination of education and experience is required.
Reference Number: 40-25219
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