Research Quality Control Specialist Oncology

Banner Medical Group

Gilbert, Arizona, US
In-person (monday - friday, 8am-4:30pm)
Bachelor's degree in life sciences or clinical research
Minimum 3 years experience in quality control or clinical research
Strong understanding of fda regulations and ich-gcp guidelines
The Research Quality Control Specialist position at Banner Medical Group in Gilbert, Arizona, focuses on ensuring the integrity and compliance of oncology clinical trials. The role requires strong experience in oncology research and quality control, as well as excellent communication and problem-solving skills

Job Summary

  • 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 is responsible for leading efforts to ensure the integrity and quality of clinical research trials by reviewing protocols, monitoring adherence, and performing audits to identify discrepancies.
  • The ideal candidate brings strong experience in oncology research along with a solid background in quality control to help refine quality processes that elevate the performance of the entire research program.

Matching Summary

Match Score: 85

The Research Quality Control Specialist position at Banner Medical Group in Gilbert, Arizona, focuses on ensuring the integrity and compliance of oncology clinical trials. The role requires strong experience in oncology research and quality control, as well as excellent communication and problem-solving skills.

Skills & Requirements

Must-have

  • Bachelor's degree in Life Sciences or Clinical Research
  • Minimum 3 years experience in quality control or clinical research
  • Strong understanding of FDA regulations and ICH-GCP guidelines
  • Proficiency in Microsoft Office Suite and clinical trial management systems

Nice-to-have

  • Prior experience in oncology or neurology research
  • Excellent communication and cross-functional teamwork skills
  • Ability to identify issues and support corrective actions

Key Requirements

  • Bachelor's degree in related field
  • Minimum 3 years of relevant experience
  • Knowledge of FDA and ICH-GCP regulations

Work Rights

Not specified

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