The Division of Clinical Research provides high-quality, efficient infrastructure support for all aspects of clinical protocol research at MD Anderson. Through our offices, we are devoted to the needs and protection of all those participating in or conducting clinical research while maintaining high ethical standards and compliance with all regulatory policies. The primary purpose of the position is to support the execution of clinical trials by collecting, processing, and managing biological specimens, maintaining laboratory equipment, and ensuring compliance with study protocols and regulatory guidelines. This role requires precise documentation, adherence to Good Clinical Laboratory Practices (GCLP), and collaboration with research teams to ensure high-quality data collection. Strong attention to detail, organizational skills, and the ability to work in a fast-paced environment are essential. The ideal candidate is detail-oriented, reliable, and professional, with a strong focus on accuracy and consistency. Experience in documentation, data entry, shipping/receiving, lab support, or quality control is preferred. Strong accountability, attention to detail, and the ability to work both independently and as part of a team are essential. Phlebotomy or specimen processing experience is a plus but not required.
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Job Type
Full-time
Career Level
Mid Level
Education Level
Associate degree