Coordinates and performs a variety of research andadministrative activities required in the management of clinical trialsresearch. Duties include assisting principal investigators and/or other membersof the research team in the development of protocols, budgets, and plans forclinical research studies; coordinating the preparation and submission ofreports, documents, and correspondence for regulatory agencies and internalreview board; interpreting and applying regulatory and policy requirements toprotocols and procedures. Provides support in recruiting, enrolling schedulingand follow up visits of clinical trial subjects. Helps to ensure adherence toFood and Drug Administration (FDA) and protocol guidelines. Identifiespotential problems and/or inconsistencies and informs supervisors as needed.Works with sponsors and grant/contract administrators to complete negotiationof clinical trials agreements. Under the general direction of the Division Director, thisposition assumes 24/7 responsibility and accountability for coordinating andimplementing a physician-sponsored Investigational Device Exemption (IDE)clinical trial under current FDA regulations. Other responsibilities includeserving as coordinator on various industry-sponsored clinical trials. This individual must be self-directed,self-motivated with good communication and interpersonal skills, be able towork independently and be flexible. Must be able to maintain the vision andmission of UAB research. Hourly Rate of Pay: $16.48 - $25.93 Bachelor's degree in a related field and two (2) years ofrelated experience required. Work experience may substitute for educationrequirement. Associated topics: clinical, clinical development, clinical informatics, clinical trial, coordinator, lab, laboratory, research, research coordinator
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