CLINICAL RESEARCH COORD A
Duties: Coordinate Sleep Research Protocols; Screen potential subjects for sleep related research protocols: Initiate Informed Consent Process for prospective research subjects; Arrange appointments; Create & maintain research databases; record ongoing study documentation i.e. Source documents, AE's & SAE's. Compile and analyze MRI data; Present and administer MRI acquisition .Collaborate with members of research team in data analysis, quality assessments and data management. Evening recruitment, one weekend a month and one, at the most two nights a week, of patients in the PCSD.
Qualifications: BA in Psychology or Social Sciences and 1 to 3 years of experience or an equivalent combination of education and experience required; background in clinical research preferred but not essential; Excellent communication & interpersonal skills (essential); Computer literate with knowledge of WORD, EXCEL and ACCESS; (ACCESS preferred) Willingness to attend series of lectures on the basic principles of clinical research (Experience dependent).
Reference Number: 40-26277
Salary Grade: 025
Employment Type: Exempt
Org: SL-Center for Sleep
Job Family: I-Technical/Professional Research