CLINICAL RESEARCH ADMINISTRATOR III (3)
University of Alabama at BirminghamAbout the role
Description
The University of Alabama at Birmingham (UAB), O'Neal Comprehensive Cancer Center, is seeking a Clinical Research Administrator III.
The O'Neal Comprehensive Cancer Center is one of 51 NCI-designated comprehensive cancer centers in the United States and is the only one in Alabama and in the Deep South region. A comprehensive designation also means UAB Medicine patients have access to leading-edge treatments or clinical trials that they may not otherwise have at local community hospitals or smaller cancer centers. For many, an NCI designation can hold the key to survival. On campus and around Birmingham, the O'Neal Cancer Center is a significant part of our economic powerhouse. The O'Neal Cancer Center powers more than 400 scientists and physician-scientists, cares for 20,000 patients annually, and is home to more than 160 employees, plus all the physicians and clinical staff engaged in cancer patient care. The link to our website is: https://www.uab.edu/onealcancercenter/
Please attach a current resume with this application.
General Responsibilities
To act as a resource for faculty and staff regarding administrative duties for industry and sponsored clinical research.
To serve as an informational and referral resource for the clinical research community.
To work with necessary parties to identify compliance, legal, IP and business/financial risk.
To manage accounts across all studies as needed.
To process and analyze reports in OnCore, as needed.
Key Duties & Responsibilities
Acts as a resource for faculty and staff regarding administrative duties for industry and sponsored clinical research.
Serves as an informational and referral resource for the clinical research community.
Works with necessary parties to identify compliance, legal, IP and business/financial risk.
Manages accounts across all studies as needed.
Conducts literature reviews. Assesses and determines solutions for operational shortcomings of protocols. Determines operational elements needed for conduct of clinical studies.
Trains staff in various work responsibilities, as needed. Provides training to office personnel in ethical conduct of research. Contributes to strategic planning within the respective Department or School, as needed.
Maintains currency in field through cross training, continuing education, literature and seminars in order to implement this knowledge and create efficiencies within the Department.
Processes and analyzes reports in OnCore, as needed.
Reviews protocol, ICF, Sponsors budget and any other study documents required to build initial calendar
Completes RedCap submission to FAP.
This also includes submission to CCTS and Tissue Procurement Submissions.
Reviews protocol amendments as they occur and makes any necessary changes to billing plan, then resubmits back to FAP.
Ancillary Department Submissions (i.e. Radiology, CCTS, Tissue Procurement).
Onboarding/training new FAP submitters.
Review of studies with clinical research coordinators
Performs other duties as assigned.
Annual Salary Range: $55,180 - $89,670
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