CLINICAL RESEARCH ADMINISTRATOR I
UAB Medicine
Description
The University of Alabama at Birmingham (UAB), O'Neal Comprehensive Cancer Center is seeking a Clinical Research Administrator I. The Clinical Research Administrator I reports to the Protocol Review Monitoring System (PRMS) Director as a navigator.
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 intake, triage, assessment and distribution of study materials.
To collect and process information related to studies.
To maintain records and documentation. To maintain study s compliance with institutional requirements.
To work with sponsors/study team to arrange required trainings and meetings.
To maintain familiarity with appropriate Good Clinical Practice (GCP) guidelines and regulations.
Key Duties & Responsibilities
Collaborates with physicians, faculty, O'Neal Clinical Trials Office staff, School of Medicine, and other departments as needed, collecting, maintaining records, and documentation to support negotiating confidentiality agreements (CDAs), contracts, and amendments related to the conduct of oncology clinical research activities.
Manages intake, triage, assessment, and distribution of oncology clinical trials under the PRMS to assure alignment with institutional review and study compliance.
Engages with sponsors/study team to arrange required trainings and Working Group meetings.
Maintains familiarity with appropriate Good Clinical Practice (GCP) guidelines and regulations.
Performs other duties as assigned.
Hourly Range: $18.85 - $30.65
Qualifications
High School diploma or GED required.
Preferences
Bachelor's degree preferred.
Knowledge of clinical trial processes.
Data collection and data entry skills.
- Knowledge of protocols and standard operating procedures (SOPs) for data quality assurance.