Clinical Trial QA/QC Technician – Specimen & Data

UT MD Anderson; Houston (TX); On-site; USD 44,000 - 66,000; Full time

Benefits offered by this job

Employer-paid medical coverage from 1^

PTO and holidays

Tuition assistance

Retirement plans

Job summary

The University of Texas MD Anderson Cancer Center seeks a detail‑oriented Clinical Trial Technician to support specimen collection, processing, labeling and data entry, ensuring compliance with GCLP and study protocols. You will collaborate with nurses, investigators, and lab teams to maintain data quality and integrity.

The role is onsite at the Texas Medical Center, with a M-F 10:00 AM - 6:30 PM schedule, offering a competitive starting salary and a comprehensive benefits package including

Qualifications

• Associate's degree in public health, healthcare administration or related field required.
• Bachelor's degree in public health, healthcare administration or related field preferred.
• Two years of experience in clinical or research laboratory setting; may substitute with additional years of related experience.
• Phlebotomy or specimen processing experience is a plus.

Responsibilities

• Collect and process biological specimens per protocol.
• Label, document, and data-entry for samples.
• Maintain regulatory compliance and audit-ready records.
• Calibrate and maintain lab equipment; manage supplies.
• Collaborate with nurses, investigators, and research teams.
• Participate in team meetings and training.

Skills

Phlebotomy

Specimen processing

Documentation/data entry

Regulatory compliance

Team collaboration

Education

Associate's Degree in Public Health/Healthcare Administration or related

Bachelor's Degree in Public Health/Healthcare Administration or related (preferred)

Tools

ASCP Certification

CCRC Certification

CCR P Certification

CRRA Certification

Job description

The University of Texas MD Anderson Cancer Center seeks a detail‑oriented Clinical Trial Technician to support specimen collection, processing, labeling and data entry, ensuring compliance with GCLP and study protocols. You will collaborate with nurses, investigators, and lab teams to maintain data quality and integrity.

The role is onsite at the Texas Medical Center, with a M-F 10:00 AM - 6:30 PM schedule, offering a competitive starting salary and a comprehensive benefits package including