Research Quality Control Specialist Oncology

Banner Health

2d•Onsite

About The Position

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.

Requirements

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.

Nice To Haves

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.

Responsibilities

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.