Clinical Trial Technician

University of Texas MD Anderson Cancer Center

Houston, Northern (TX, KY)

Hybrid

USD 44,000 - 66,000

Full time

4 days ago

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Benefits offered by this job

Medical coverage

PTO & holidays

Tuition assistance

Pension

Job summary

The University of Texas MD Anderson Cancer Center seeks a Clinical Trial Technician to support phase 1 trials by collecting, processing, and managing biological specimens and ensuring compliance with study protocols.

Responsibilities include phlebotomy, performing EKGs, maintaining laboratory equipment, and collaborating with nurses and investigators to ensure accurate data collection. Onsite work in Texas Medical Center with competitive benefits.

Qualifications

Two years of experience in a clinical or research laboratory setting. With preferred degree, no experience required.
Preferred: prior blood-drawing experience; EKG and specimen processing a plus.
May substitute education degree with additional years of related experience.

Responsibilities

Specimen Collection and Processing per protocol, including phlebotomy and storage.
Perform electrocardiograms (EKGs) according to study requirements.
Maintain labeling, documentation, and data entry for specimens.
Assist in equipment maintenance, calibration, and inventory control.
Ensure regulatory compliance and participate in quality control activities.

Skills

Phlebotomy

EKG

Specimen processing

Documentation

GCLP compliance

Team collaboration

Education

Associate's Degree in Public Health/Healthcare Administration

Bachelor's Degree preferred

Tools

Phlebotomy equipment

Laboratory instruments

Job description

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

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 (60%)

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.

Regulatory Compliance and Quality Assurance (20%)

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.

Laboratory Operations and Collaboration (20%)

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.

Additional Duties

Perform other duties as assigned in support of clinical trial operations and laboratory activities.

EDUCATION

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

WORK EXPERIENCE

Required: Two years of experience in a clinical or research laboratory setting. With preferred degree, no experience required
Preferred: Prior Blood drawing experience is a must. Prior experience with EKG and specimen processing is a plus
May substitute required education degree with additional years of related experience on a one-to-one basis

LICENSES AND CERTIFICATIONS

Preferred: 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)
Preferred: CCRC - Certified Clinical Research Coordinator
Preferred: CCRP - Certified Clinical Research Professional
Preferred: 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