Clinical Trial Technician - Clinical Trials Lab Services

The MD Anderson Clinical Trials Lab Services (CTLS) team is seeking a Clinical Trial Technician 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.

The ideal candidate thrives in a fast-paced laboratory environment and demonstrates exceptional attention to detail while managing multiple tasks efficiently. They possess EKG experience and hold a phlebotomy certification (ASCP), ensuring high standards of patient care and specimen collection. Strong organizational skills, adaptability, and the ability to maintain accuracy under pressure are essential for success in this role.

*This position is 100% onsite with the schedule of 3:30pm-11:30pm.*

MD Anderson Offers Employees

• Paid employee medical benefits (zero premium) starting on first day for employees who work 30 or more hours per week.
• Group Dental, Vision, Life, AD&D and Disability coverage.
• Paid time off (PTO) and Extended Illness Bank (EIB) paid leave accruals.
• Paid institutional holidays, wellness leave, childcare leave, and other paid leave programs.
• Tuition Assistance Program after six months of service.
• Teachers Retirement System defined-benefit pension plan and two voluntary retirement plans.
• Employer paid life, AD&D and an illness-related reduced salary pay program.
• Opportunities for professional growth through Career Development Center and Mentoring programs.
  
  

Key Functions

Specimen Collection and Processing (60%)

• Perform biological specimen collection, including phlebotomy and electrocardiograms (EKGs), according to protocol guidelines.
• Process and store specimens according to protocol requirements, including centrifugation for plasma or serum extraction.
• Ensure accurate labeling, documentation, and data entry for all collected specimens.
• Maintain specimen integrity by adhering to temperature and handling requirements.
• Assist in troubleshooting specimen-related issues and deviations.
  
  

Regulatory Compliance and Quality Assurance (20%)

• Follow all institutional, federal, and sponsor-specific regulatory guidelines for clinical research.
• Ensure adherence to Standard Operating Procedures (SOPs) and study protocols.
• Maintain thorough and accurate records to support regulatory audits and inspections.
• Participate in quality control measures to ensure protocol compliance.
• Report deviations, adverse events, and safety concerns to the appropriate personnel.
  
  

Laboratory Operations and Collaboration (20%)

• Assist in laboratory equipment maintenance, calibration, and troubleshooting.
• Maintain inventory of research kits and laboratory supplies, ensuring availability for study needs.
• Communicate effectively with clinical research teams, nurses, and investigators.
• Support process improvement initiatives to enhance laboratory efficiency.
• Participate in team meetings and training sessions to stay updated on best practices.
  
  

EDUCATION

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

Work Experience

• Required: 2 years Experience in clinical or research laboratory setting, OR with preferred degree, no experience.
  
  

May substitute required education degree with additional years of related experience on a one to one basis.

• Preferred: 2 years Experience in phlebotomy and laboratory processing.
  
  

LICENSES AND CERTIFICATIONS

• Preferred: From one of the following:
• 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
  

The University of Texas MD Anderson Cancer Center offers excellent benefits , including medical, dental, paid time off , retirement , tuition benefits, educational opportunities, and individual and team recognition.

This position may be responsible for maintaining the security and integrity of critical infrastructure, as defined in Section 113.001(2) of the Texas Business and Commerce Code and therefore may require routine reviews and screening. The ability to satisfy and maintain all requirements necessary to ensure the continued security and integrity of such infrastructure is a condition of hire and continued employment.

It is the policy of The University of Texas MD Anderson Cancer Center to provide equal employment opportunity without regard to race, color, religion, age, national origin, sex, gender, sexual orientation, gender identity/expression, disability, protected veteran status, genetic information, or any other basis protected by institutional policy or by federal, state, or local laws unless such distinction is required by law. http://www.mdanderson.org/about-us/legal-and-policy/legal-statements/eeo-affirmative-action.html

Additional Information

• Requisition ID: 177733
• Employment Status: Full-Time
• Employee Status: Regular
• Work Week: Days, Evening/Night
• Minimum Salary: US Dollar (USD) 44,000
• Midpoint Salary: US Dollar (USD) 55,000
• Maximum Salary : US Dollar (USD) 66,000
• FLSA: non-exempt and eligible for overtime pay
• Fund Type: Soft
• Work Location: Onsite
• Pivotal Position: No
• Referral Bonus Available?: No
• Relocation Assistance Available?: No