Research Quality Auditor job at OneOncology in US National
Title: Research Quality Auditor
locations
United States
time type
Full time
job requisition id
R-0000019282
Job Description:
OneOncology is positioning community oncologists to drive the future of cancer care through a patient-centric, physician-driven, and technology-powered model to help improve the lives of everyone living with cancer. Our team is bringing together leaders to the market place to help drive OneOncology’s mission and vision.
Why join us? This is an exciting time to join OneOncology. Our values-driven culture reflects our startup enthusiasm supported by industry leaders in oncology, technology, and finance. We are looking for talented and highly-motivated individuals who demonstrate a natural desire to improve and build new processes that support the meaningful work of community oncologists and the patients they serve.
Job Description:
The Research Quality Auditor will report to the Manager, Research Quality. This individual will collaborate with various OneOncology Research Network (OneR) teams and OneOncology practices to support clinical research across the OneR network. The Research Quality Auditor plays a vital role in ensuring the integrity, accuracy, and compliance of clinical trials with established regulations and standards.
The Research Quality Auditor is responsible for evaluating clinical trials for compliance with Good Clinical Practice (GCP), regulatory requirements, quality standards, and best practices throughout the lifecycle of clinical trials. This position ensures that clinical trials are conducted, recorded, and reported in accordance with GCP, while also ensuring that data integrity is maintained. This position requires a keen eye for detail, strong analytical skills, and a deep understanding of clinical research processes and regulations. The Research Quality Auditor also supports quality management initiatives and contributes to continuous improvement efforts to enhance the overall quality and integrity of research.
Key Responsibilities
Plan, organize, and conduct GCP audits of network sites and clinical trial systems/processes
Contribute to the audit schedule and prepare audit plans, using a risk-based approach
Inspect trial records, data, documentation, and facilities to ensure compliance with GCP guidelines, regulatory requirements, site SOPs, and the protocol as applicable
Lead audit kickoff and wrap-up meetings; interview clinical site staff (investigators, coordinators, etc.) to assess processes, procedures, and adherence to regulatory standards
Document audit observations via standardized tools
Prepare audit reports that detail nonconformities and findings and provide required actions and/or recommendations for bringing the site back into compliance as applicable
Track audit findings and required actions through to resolution, including assisting in Corrective and Preventive Action Plan development and process improvement as applicable
Ensure audit documentation is accurate, complete, and organized
Prepare periodic reports and metrics to communicate audit status and relevant outcomes to relevant stakeholders and OneR leadership
Participate in qualification activities and audits of network-level vendors by performing vendor risk assessments, liaising with vendor representatives to complete vendor questionnaires, and working with cross-functional OneR teams (e.g., Operations, Research Product) to establish vendor oversight plans
Identify areas for improvement in site-level and network-level processes and procedures
Stay informed of current clinical trial regulations, requirements, and guidance from FDA, ICH, and other relevant regulatory authorities
Support regulatory inspections, sponsor/CRO audits, and inquiries by preparing documentation and addressing findings as needed
Participate in audit- and inspection-readiness activities
Assist in the development, implementation, and maintenance of quality management systems to ensure compliance with regulatory requirements, industry standards, and organizational policies
Participate in the development and review of SOPs and work instructions to promote consistency and compliance in clinical research operations
Assist in developing training materials and resources to enhance research staff understanding of practical application of regulatory requirements and best practices
Other duties as assigned to help drive our mission of improving the lives of everyone living with cancer.
Key Competencies
Strong attention to detail
Ability to make critical and objective assessments and sound judgement calls
Demonstrated problem-solving and analytical capabilities
Excellent written and verbal communication skills
Excellent interpersonal and organizational skills to create and maintain effective working relationships within OneR and with OneOncology practice partners
Ability to initiate assigned tasks and work independently
Ability to manage multiple projects in various stages and adhere to timelines
Qualifications
Minimum of 3-5 years of experience in clinical research, including at least 2 years of clinical trial auditing experience
Bachelor’s degree required
Demonstrated knowledge of GCP, FDA regulations, ICH guidelines, and clinical trial quality assurance auditing techniques
Experience supporting FDA inspections highly preferred
Proficiency in Microsoft Office applications and familiarity with quality management systems, electronic data capture (EDC) systems, electronic regulatory binders, and clinical trial management systems (CTMS)
Clinical research and/or quality assurance certification highly preferred
Remote (U.S.-based) with ability to travel ~25% (mostly within the southeastern U.S.)
#LI-REMOTE
Apply Now
Apply Now
locations
United States
time type
Full time
job requisition id
R-0000019282
Job Description:
OneOncology is positioning community oncologists to drive the future of cancer care through a patient-centric, physician-driven, and technology-powered model to help improve the lives of everyone living with cancer. Our team is bringing together leaders to the market place to help drive OneOncology’s mission and vision.
Why join us? This is an exciting time to join OneOncology. Our values-driven culture reflects our startup enthusiasm supported by industry leaders in oncology, technology, and finance. We are looking for talented and highly-motivated individuals who demonstrate a natural desire to improve and build new processes that support the meaningful work of community oncologists and the patients they serve.
Job Description:
The Research Quality Auditor will report to the Manager, Research Quality. This individual will collaborate with various OneOncology Research Network (OneR) teams and OneOncology practices to support clinical research across the OneR network. The Research Quality Auditor plays a vital role in ensuring the integrity, accuracy, and compliance of clinical trials with established regulations and standards.
The Research Quality Auditor is responsible for evaluating clinical trials for compliance with Good Clinical Practice (GCP), regulatory requirements, quality standards, and best practices throughout the lifecycle of clinical trials. This position ensures that clinical trials are conducted, recorded, and reported in accordance with GCP, while also ensuring that data integrity is maintained. This position requires a keen eye for detail, strong analytical skills, and a deep understanding of clinical research processes and regulations. The Research Quality Auditor also supports quality management initiatives and contributes to continuous improvement efforts to enhance the overall quality and integrity of research.
Key Responsibilities
Plan, organize, and conduct GCP audits of network sites and clinical trial systems/processes
Contribute to the audit schedule and prepare audit plans, using a risk-based approach
Inspect trial records, data, documentation, and facilities to ensure compliance with GCP guidelines, regulatory requirements, site SOPs, and the protocol as applicable
Lead audit kickoff and wrap-up meetings; interview clinical site staff (investigators, coordinators, etc.) to assess processes, procedures, and adherence to regulatory standards
Document audit observations via standardized tools
Prepare audit reports that detail nonconformities and findings and provide required actions and/or recommendations for bringing the site back into compliance as applicable
Track audit findings and required actions through to resolution, including assisting in Corrective and Preventive Action Plan development and process improvement as applicable
Ensure audit documentation is accurate, complete, and organized
Prepare periodic reports and metrics to communicate audit status and relevant outcomes to relevant stakeholders and OneR leadership
Participate in qualification activities and audits of network-level vendors by performing vendor risk assessments, liaising with vendor representatives to complete vendor questionnaires, and working with cross-functional OneR teams (e.g., Operations, Research Product) to establish vendor oversight plans
Identify areas for improvement in site-level and network-level processes and procedures
Stay informed of current clinical trial regulations, requirements, and guidance from FDA, ICH, and other relevant regulatory authorities
Support regulatory inspections, sponsor/CRO audits, and inquiries by preparing documentation and addressing findings as needed
Participate in audit- and inspection-readiness activities
Assist in the development, implementation, and maintenance of quality management systems to ensure compliance with regulatory requirements, industry standards, and organizational policies
Participate in the development and review of SOPs and work instructions to promote consistency and compliance in clinical research operations
Assist in developing training materials and resources to enhance research staff understanding of practical application of regulatory requirements and best practices
Other duties as assigned to help drive our mission of improving the lives of everyone living with cancer.
Key Competencies
Strong attention to detail
Ability to make critical and objective assessments and sound judgement calls
Demonstrated problem-solving and analytical capabilities
Excellent written and verbal communication skills
Excellent interpersonal and organizational skills to create and maintain effective working relationships within OneR and with OneOncology practice partners
Ability to initiate assigned tasks and work independently
Ability to manage multiple projects in various stages and adhere to timelines
Qualifications
Minimum of 3-5 years of experience in clinical research, including at least 2 years of clinical trial auditing experience
Bachelor’s degree required
Demonstrated knowledge of GCP, FDA regulations, ICH guidelines, and clinical trial quality assurance auditing techniques
Experience supporting FDA inspections highly preferred
Proficiency in Microsoft Office applications and familiarity with quality management systems, electronic data capture (EDC) systems, electronic regulatory binders, and clinical trial management systems (CTMS)
Clinical research and/or quality assurance certification highly preferred
Remote (U.S.-based) with ability to travel ~25% (mostly within the southeastern U.S.)
#LI-REMOTE
Apply Now
Apply Now