Duties: The position involves complex and sensitive tasks related to conducting several Phase II/III clinical trials including the following: 1) recruit and scheduling subjects for the numerous aspects of the study in strict accordance with the research protocol, 2) administer study interventions, which may involve health coaching, motivational interviews, and mobile device (smartwatch/smartphone)-based interventions, 3) Ensure compliance in strict accordance with FDA (Investigational Drug Application), NIH, Institutional Review Board (IRB), and Office for Clinical Research (OCR) guidelines (this includes yearly progress reports to each agency and reporting of protocol changes), and 4) managing the study subject database. Prior experience with clinical research is required. In this position, the staff member will be responsible, with the Principal Investigator, for the effective conduct of research and safety of research subjects.

Qualifications: A Bachelor's degree and 2 to 4 years of experience or an equivalent combination of education and experience required.

Reference Number: 40-26390

Salary Grade: 026

Employment Type: Exempt

Org: DM-Geriatrics

Special Requirements:

Job Family: I-Technical/Professional Research

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