T221663 - University of Alabama at Birmingham

The University of Alabama at Birmingham (UAB), O'Neal Comprehensive Cancer Center is seeking a Clinical Research Coordinator I.

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 coordinator for studies and provide support to other team members within the confines of the protocol as directed.
• To support screening and participant eligibility determination, working with more senior team members to ensure compliance.
• To conduct activities in accordance with the protocol, regulations and Good Clinical Practice (GCP).
• To assist with the study life cycle from start-up to closure, i.e., collecting and recording data, recruiting and performing follow-up with participants, scheduling visits and assisting in coordination of lab and fieldwork.

Key Duties & Responsibilities

1. Collects and records preliminary data for clinical research programs.
2. Recruits and performs follow-up with research participants as protocols outline.
3. Schedules visits according to research protocols.
4. Assists in the coordination of lab and fieldwork.
5. Prepares for study monitoring visits.
6. Assists with correcting findings.
7. Assists with the completion of Case Report Forms (CRF) according to protocol.
8. Assists with the development of protocols and standard operating procedures (SOPs) for data quality assurance.
9. Performs general clerical duties (faxing, scanning, routing messages, coordinating the purchase of study supplies/materials).
10. May perform a variety of medical procedures under supervision.
11. May assist in compiling, editing, and proofing written reports for both internal and external administrative offices.
12. May perform data analysis using a variety of software packages.
13. Uses Electronic Data Capture (EDC) systems necessary for operations under supervision.
14. Must be able to walk 1 - 1.5 miles/day. Able to bend, stand, and lift up to 10 lbs.
15. Performs other duties as assigned.

Annual Salary Range:%2443,890 - %2471,320

High School diploma or GED required.

Preferences

• Prefer candidates with a bachelor's and two (2) years experience working in a clinical setting.
• Knowledge of clinical trial processes, data collection, and data entry.
• Knowledge of medical terminology.
• Experience with recruiting and performing follow-up with research participants as protocols outline.
• Knowledge of protocols and standard operating procedures (SOPs) for data quality assurance.

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, religion, sexual orientation, gender identity, gender expression, and veteranrsquo;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 UABrsquo;s Assistant Vice President and Senior Title IX Coordinator. The Title IX notice of nondiscrimination is located at uab.edu/titleix.