T230452

ng-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 prepare, submit, and assist with multiple levels of research documentation (i.e. IRB submissions, educational materials, reports, grant renewal reports, and study forms).
• To maintain regulatory documentation including consent forms, protocols, 1572s, CVs, licenses, investigator brochures, recruitment materials, safety reports, and submission forms.
• To draft informed consents.
• To prepare and maintain FDA applications for Investigational New Drugs (INDs) and Investigational Device Exemptions (IDEs).
• To assist in drafting compliant advertisements.
• To serve as resource person or act as consultant within area of regulatory expertise.

Key Duties & Responsibilities
• Prepares, submits, and assists with multiple levels of research documentation (i.e. FDA, IRB submissions, educational materials, reports, grant renewal reports, and study forms). Maintains regulatory documentation, including consent forms, protocols, 1572s, CVs, licenses, investigator brochures, recruitment materials, safety reports, and submission forms. Knowledge of GCP (Good Clinical Practice).
• Prepares and maintains FDA applications, deviations, and SAE (serious adverse events) documents.
• Makes and assists in modifying protocols and study documents. Completes and submits safety reports and government documents as needed. Enters protocol-specific data into required institutional systems (IRAP and OnCore).
• Maintains appropriate licensure for clinicians. Conducts internal quality assurance audits of regulatory files. Oversees maintenance of Delegation of Authority logs. Maintain the study's compliance with institutional requirements.
• Assists colleagues in identifying efficiencies and improving processes.
• Serves as a mentor to junior regulatory staff. May train others in various work responsibilities and provide constructive feedback.
• Performs other duties as assigned.

Annual Salary Range:%2447,665 - %2477,455

Bachelor's degree in a related field and three (3) years of related experience required. Work experience may substitute for education requirement.

Preferences
• Preferred degree: Health Care or related field.
• Knowledge of regulatory processes and ICH-GCP guidelines is involved to ensure studies comply with regulations, ethical guidelines, and policies.
• Experience with preparing FDA, IRB, deviation, and SAE submissions applicable to clinical trials.
• Strong communication and relationship-building skills.
• Prior experience in the clinical trial regulatory environment, interacting with sponsors, regulatory authorities, and investigators.
• Ability to communicate effectively with physicians, sponsors, and other collaborators independently.

UAB is an Equal Employment/Equal Educational Opportunity Institution dedicated to providing equal opportunities and equal access to all individuals regardless of race, color, religion, ethnic or national origin, sex (including pregnancy), genetic information, age, disability, and veteran's status. As required by Title IX, UAB prohibits sex discrimination in any education program or activity that it operates. Individuals may report concerns or questions to UAB's Assistant Vice President and Senior Title IX Coordinator. The Title IX notice of nondiscrimination is located at uab.edu/titleix.
University310008400 Comprehensive Cancer CenterRegular

About the Company:
University of Alabama at Birmingham