"CLINICAL RESEARCH DATA COORDINATOR II (5)"

The University of Alabama at Birmingham (UAB), O'Neal Comprehensive Cancer Center is seeking a Clinical Research Data 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 design, implement and maintain clinical-based relational database management systems.
• To ensure operation and maintenance of departmental systems for data organization, collection, retrieval, and reporting purposes.
• To develop methods for tracking and reporting data and monitors incoming and outgoing data to ensure data integrity and compliance with applicable regulatory agency policy.
• To research and collect information and enter data into established external data marts specific to clinical discipline and retrieves as necessary.
• To perform a variety of statistical analyses and summarizes results.
• Performs other duties as assigned.

Annual Salary Range: $45,395 - $73,770

Qualifications

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.
• Clinical trial research, knowledge of applicable clinical research data collection requirements, including GCP and ICH guidelines.
• Strong clinical data entry skills.
• Familiar with patient records and documentation.
• Strong background using medical terminology.
• Exposure to patient care in a hospital or outpatient setting.
• Oncology or general medical background.
• Experience reading charts and extracting information.
• Experience as part of a medical team.
• Strong communication and relationship-building skills.