Clinical Trial Technician QAQC

University of Texas MD Anderson Cancer Center

Houston (TX)

On-site

USD 44,000 - 66,000

Full time

13 days ago

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Benefits offered by this job

Medical coverage from day one

Paid time off

Tuition assistance

Pension plan

Job summary

The University of Texas MD Anderson Cancer Center is seeking a detail-oriented specimen collection and processing specialist to support clinical trial workflows at the Texas Medical Center. You will collect, process, and store specimens, maintain lab equipment, and ensure data accuracy and regulatory adherence.

Required associate degree with two years in a clinical or research lab; bachelor’s preferred. Phlebotomy or specimen processing experience is a plus.

Qualifications

Two years in a clinical or research laboratory setting.
Associate's degree required; Bachelor's preferred.
Detail-oriented with strong documentation and data entry skills.
Ability to work independently and in a team.

Responsibilities

Perform specimen collection and processing per protocol.
Label, document, and data entry for collected specimens.
Store specimens maintaining integrity and proper storage conditions.
Troubleshoot specimen-related issues and protocol deviations.
Maintain regulatory compliance and support audits.
Collaborate with clinical researchers, nurses, and investigators.

Skills

Phlebotomy

Specimen processing

Documentation

Data entry

Shipping/receiving

Lab support

Quality control

Regulatory compliance

Education

Associate's Degree Public Health/Healthcare Admin or related field

Bachelor's Degree Public Health/Healthcare Admin or related field

Job description

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.

Minimum $21.15 - Midpoint $26.44 - Maximum $31.73

The typical work schedule is M-F 10:00 AM - 6:30 PM (Mid shift)

Work Location: Texas Medical Center

Why Us?

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.

Responsibilities

Specimen Collection and Processing

Perform biological specimen collection, including phlebotomy for blood, urine, tissue, and electrocardiograms according to protocol guidelines
Process and store specimens per protocol requirements, including centrifugation for plasma or serum extraction
Ensure accurate specimen labeling, documentation, and data entry for all collected specimens
Maintain specimen integrity by adhering to temperature and handling requirements
Assist with troubleshooting specimen-related issues and protocol deviations

Regulatory Compliance and Quality Assurance

Follow institutional, federal, and sponsor-specific regulatory guidelines for clinical research
Adhere to Standard Operating Procedures and study protocols
Maintain thorough and accurate records to support regulatory audits and inspections
Participate in quality control activities to ensure protocol compliance
Report deviations, adverse events, and safety concerns to appropriate personnel

Laboratory Operations and Collaboration

Assist with laboratory equipment maintenance, calibration, and troubleshooting
Maintain inventory of research kits and laboratory supplies to support 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 remain current on best practices

Other Duties

Perform other duties as assigned

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: Two 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: Experience in documentation, data entry, shipping/receiving, lab support, or quality control is preferred. Phlebotomy or specimen processing experience is a plus

LICENSES AND CERTIFICATIONS

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 - Cert Clin Research Assoc

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