University of Alabama at Birmingham

The University of Alabama at Birmingham (UAB), O'Neal Comprehensive Cancer Center is seeking a Clinical Research Coordinator II.. 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.. On campus and around Birmingham, the O'Neal Cancer Center is a significant part of our economic powerhouse.. Knowledge of regulatory/compliance affairs as it pertains to clinical research.

clinical research coordinator ii

The University of Alabama at Birmingham (UAB), O'Neal Comprehensive Cancer Center is seeking a Clinical Research Coordinator II.
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 serve as a liaison with medical staff, University Departments, ancillary departments and/or satellite facilities.
* To organize patient enrollment planning.
* To conduct quality assurance activities.
* To compile and analyze data.
* To develop and implement procedures, maintain records, track progress, and conduct quality assurance on data collected.
* To serve as a mentor to junior staff, including student assistants.
Key Duties & Responsibilities
* Screens and enrolls participants in Oncology clinical trials.
* Conducts informed consent per GCP guidelines.
* Conducts patient visits per protocol schedule of events.
* Follows clinical trial budget with each visit.
* Documents adverse events, medications, and procedures conducted at each visit.
* Prepares lab kits for each patient visit, Administers EKGs, Quality of Life, and other procedures as trained.
* Works with sponsors to answer visit queries.
* Conducts Study initiation visits.
* Conducts point-of-care protocol training.
* Assists the PI and nursing in developing protocol orders.
* Attends team meetings and educational training as required.
* Performs other duties as assigned.
Annual Salary Range: $50,050 - $81,330
Bachelor's degree in a related field and three (3) years of related experience required. Work experience may substitute for education requirement.
Preferences
* Clinical Research experience, science, and medical terminology.
* Assisting with the coordination of research activities involved in conducting Oncology clinical trials. Management of data and study patients' care.
* Knowledge of regulatory/compliance affairs as it pertains to clinical research.<br/><br/>#J-18808-Ljbffr

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