Clinical Trial Technician

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.

Minimum $21.15/hour
- Midpoint $26.44/hour
- Maximum $31.73/hour

Work Location:

Texas Medical Center

Schedule:

Onsite

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

• 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.

• Required:
  
  Associate's Degree in Public Health, Healthcare Administration, or a related scientific field
• Preferred:
  Bachelor's Degree in Public Health, Healthcare Administration, or a related scientific field

• Required:
  
  Two years of experience in a clinical or research laboratory setting. With preferred degree, no…