Details
Posted: 10-May-24
Location: Birmingham, Alabama
Type: Full-time
Salary: Open
Categories:
Staff/Administrative
Internal Number: T213742
MANAGER-CLINICAL RESEARCH COORDINATION - (T213742)
Description
The University of Alabama at Birmingham (UAB), O'Neal Comprehensive Cancer Center is seeking a Manager-Clinical Research Coordination to provide oversight and management for the day-to-day efforts of the Cancer Center Clinical Trials Office focused cancer research coordination in conducting study activities including complex protocols in accordance with the protocol, IRB regulations, and Good Clinical Practice (GCP).
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 manage all aspects of research program and clinical studies including education/teaching.
- To oversee and manage multiple clinical research protocols and the associated personnel.
- To design best practices for management of IP for drug, device, and biologic studies.
- To prepare study budgets.
- To manage research staff within area including all applicable human resources functions.
Key Duties & Responsibilities
Annual Salary Range: $70,425 - $114,440
Bachelor's degree in a related field and eight (8) years of related experience required. Work experience may NOT substitute for education requirement. Certified Clinical Research Coordinator (CCRC) or Certified Clinical Research Professional (CCRP) certification strongly preferred.
Qualifications
Preferences
Demonstrated experience in staffing, resourcing, and scheduling clinical study coordinator teams to meet the needs of a diverse portfolio of research studies, including Sponsors, investigators, and patient needs.
Primary Location
: University
Job Category
: Clinical Research
Organization
: 310008400 Comprehensive Cancer Center
Employee Status
: Regular
Shift: Day/1st Shift
Work Arrangement (final schedule to be determined by the department/hiring manager): Onsite
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