Clinical Trial Technician

UT MD Anderson Cancer Center•Houston, TX

2d•Onsite

About The Position

The Department of Investigational Cancer Therapeutics conducts broad Phase 1 studies across disease boundaries and molecular targets. We strive to provide outstanding patient care while performing innovative Phase 1 trials with new drugs that may eventually improve the management of cancer. The primary purpose of the Clinical Trial Technician 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 Clinical Trial Technician must have prior blood-drawing experience, with EKG and specimen processing preferred. Candidates should also demonstrate a stable work history and reliability.

Requirements

Associate's Degree in Public Health, Healthcare Administration, or a related scientific field
Two years of experience in a clinical or research laboratory setting. With preferred degree, no experience required
Prior Blood drawing experience is a must.

Nice To Haves

Bachelor's Degree in Public Health, Healthcare Administration, or a related scientific field
Prior experience with EKG and specimen processing is a plus
ASCP - American Society of Clinical Pathologist Certification by American Society of Clinical Pathologist Board of Registry (BOR) or American Certification Agency (ACA) to include Phlebotomy (PBT), Medical Laboratory Technician (MLT), Medical Laboratory Assistant (MLA)
CCRC - Certified Clinical Research Coordinator
CCRP - Certified Clinical Research Professional
CCRA - Certified Clinical Research Associate

Responsibilities

Perform biological specimen collection, including phlebotomy of blood and collection of urine and tissue samples according to protocol guidelines.
Perform electrocardiograms (EKGs) according to study protocol requirements.
Process and store specimens according to protocol requirements, including centrifugation for plasma and serum extraction.
Ensure accurate labeling, documentation, and data entry for all collected specimens.
Maintain specimen integrity through adherence to required temperature controls and handling procedures.
Assist in troubleshooting specimen-related issues and protocol deviations.
Follow institutional, federal, and sponsor-specific regulatory guidelines for clinical research.
Ensure compliance with Standard Operating Procedures (SOPs) and study protocols.
Maintain thorough and accurate records supporting regulatory audits and inspections.
Participate in quality control activities to ensure protocol compliance.
Report deviations, adverse events, and safety concerns to appropriate personnel.
Assist with laboratory equipment maintenance, calibration, and troubleshooting.
Maintain inventory of research kits and laboratory supplies to support study activities.
Communicate effectively with clinical research teams, nurses, and investigators.
Support process improvement initiatives focused on laboratory efficiency.
Participate in team meetings and training sessions to remain current on best practices.
Perform other duties as assigned in support of clinical trial operations and laboratory activities.

Benefits

Employer-paid medical coverage starting day one for employees working 30+ hours/week
optional group dental, vision, life, AD&D, and disability insurance
Accruals for PTO and Extended Illness Bank
paid holidays
wellness
childcare
other leave options
Tuition Assistance Program after six months of service
access to extensive wellness, fitness, and employee resource groups
Defined-benefit pension through the Teachers Retirement System
voluntary retirement plans
employer-paid life and reduced salary protection programs