Research Quality Control Specialist Oncology

Primary City/State

Gilbert, Arizona

Department Name

BMDACC Gateway Oncology-Rsrch

Work Shift

Day

Job Category

Research

Find your path in health care. We want to change the lives of those in our care – and the people who choose to take on this challenge. If you’re ready to change lives, we want to hear from you.

The Research Quality Control Specialist plays a key role in safeguarding the integrity, accuracy, and regulatory compliance of oncology clinical trials within the Banner MD Anderson Cancer Center research program. This position leads quality-focused oversight across all phases of clinical research, partnering closely with study teams and internal and external compliance groups to ensure protocols are followed, data is reliable, and study conduct meets the highest standards set by federal regulations and Good Clinical Practice guidelines. The role is deeply collaborative, serving as both a reviewer and a resource to teams by identifying issues, supporting corrective actions, and helping refine quality processes that elevate the performance of the entire research program.

The ideal candidate brings strong experience in oncology research along with a solid background in quality control or substantial hands‑on clinical research operations. They will have a keen eye for detail, a clear understanding of regulatory expectations, and the ability to interpret complex study requirements. Someone who excels in communication, problem‑solving, and cross-functional teamwork will thrive in this role, helping ensure that every clinical trial conducted meets Banner MD Anderson’s commitment to excellence, patient safety, and scientific rigor.

Schedule : Monday - Friday 8am-4:30pm

Banner Alzheimer's Institute (BAI) was established in 2006 as Banner Health's first Center of Excellence. Banner Sun Research Health Institute (BSHRI) was founded in 1986. Our team is uniquely, passionately, and strategically committed to ending Alzheimer's disease and other neurodegenerative disorders without losing another generation and to providing an unparalleled model of care for families facing this devastating disease. Banner Research is committed to improving people's lives through comprehensive patient care and advances that capitalize on the best biomedical research. We intend to make a transformational difference in Alzheimer's disease and other neurodegenerative disorders research and care.

Position Summary

This position is responsible for leading the efforts to ensure the integrity and quality of clinical research trials. Responsible for reviewing and monitoring clinical research trials to ensure compliance with regulatory standards, protocols, and company policies. This role involves close collaboration with research teams, data management personnel, and regulatory bodies to maintain the highest standards of quality and accuracy in clinical trial data.

Core Functions

• Conduct thorough reviews of clinical trial protocols, informed consent documents, and case report forms.
• Monitor ongoing clinical trials to ensure adherence to study protocols and regulatory requirements.
• Perform audits of clinical trial data to identify discrepancies and ensure data integrity.
• Collaborate with research teams to resolve any issues related to trial conduct and data collection.
• Prepare and present detailed reports on the findings of quality control reviews.
• Assist in the development and implementation of quality control procedures and best practices.
• Stay updated on industry regulations and guidelines to ensure compliance.
• Provide training and support to research staff on quality control processes and standards.

Minimum Qualifications

Bachelor's degree in a related field (e.g., Life Sciences, Clinical Research, Quality Assurance).

Minimum of 3 years of experience in quality control or clinical research.

Strong understanding of clinical trial processes and regulatory requirements (e.g., FDA, ICH-GCP).

Excellent attention to detail and analytical skills. Effective communication and interpersonal skills. Ability to work independently and as part of a team. Proficiency in Microsoft Office Suite and clinical trial management systems. Must be knowledgeable of data entry and computer programs associated with maintaining databases, spreadsheets, etc.

Preferred Qualifications

Prior experience in quality control or quality assurance in support of clinical trials.

Experience in clinical research specific to the relevant disease indication (e.g., Oncology, Neurology, or related fields) is highly preferred.

Additional Related Education And/or Experience Preferred.

EEO Statement

EEO/Disabled/Veterans

Our organization supports a drug-free work environment.