Clinical Research Assistant

UAB St. Vincent's•Birmingham, AL

2d•Onsite

About The Position

Participate in the design, administration and monitoring of clinical trials. Plan, organize, perform and monitor daily project protocols. Collect, prepare and maintain required research documentation, such as informed consent records, case records, clinical notes and medical reports. Report and assist with the management of protocol deviations, adverse events and other project-related issues. Assist with the preparation and delivery of internal and external presentations, conference reports and lectures, and publishing submissions. Understanding of the Food and Drug Administration (FDA) rules is beneficial. About UAB St. Vincent’s UAB St. Vincent’s, a proud part of UAB Medicine, is a trusted provider of health care, serving Alabama for more than 125 years. With five hospitals and numerous clinics, we're a health care community deeply rooted in compassion, service, and respect for all, guided by the rich legacy of the St. Vincent’s name. We're committed to extending kindness and personalized care to patients, their families, and each other. We address the physical, psychological, social, and spiritual needs of our patients. We believe in the power of teamwork and unity, and foster a collaborative spirit among our more than 4,800 employees. As one of Alabama’s best hospitals as recognized by U.S. News & World Report, improving the health and lives of those we serve is at the heart of our mission. Join us in continuing our legacy of service and healing in central Alabama, where we can make a lasting impact together.

Requirements

High School diploma equivalency with 2 years of cumulative experience OR Associate'sdegree/Technical degree OR 4 years of applicable cumulative job specific experience required.

Nice To Haves

Phlebotomy experience with adults of all age ranges
research experienced preferred but not required
Understanding of the Food and Drug Administration (FDA) rules is beneficial.

Responsibilities

Participate in the design, administration and monitoring of clinical trials.
Plan, organize, perform and monitor daily project protocols.
Collect, prepare and maintain required research documentation, such as informed consent records, case records, clinical notes and medical reports.
Report and assist with the management of protocol deviations, adverse events and other project-related issues.
Assist with the preparation and delivery of internal and external presentations, conference reports and lectures, and publishing submissions.