The Minnesota Cancer Clinical Trials Network (MNCCTN) is a multi-site cancer clinical trials network. The network, led by the Masonic Cancer Center (MCC) at the University of Minnesota (UMN), brings cancer clinical trials from the Masonic Cancer Center, Mayo Clinic Cancer Center, Hormel Institute and partner institutions to community sites across the state. As a growing program, MNCCTN offers qualified candidates the opportunity to join a team that is shaping the direction and implementation of cancer clinical research across the state.
The CRA and Quality Specialist is a member of the networks coordinating center and reports to MNCCTNs Director of Operations and works closely with MNCCTN Partners and sites, investigators, and study teams the UMN and Mayo Clinic Cancer Center, UMN Masonic Cancer Centers CTO, CTSI, and other research groups or organizations. As a key member of the MNCCTN Portfolio team, the CRA and Quality Specialists primary responsibility is to develop and execute quality assurance and monitoring strategies during clinical studies/trials to ensure compliance with regulations, applicable standards, and corporate policies. Evaluates overall risk levels and audits research activities for conformance to requirements throughout the study. Develops and assesses the effectiveness of corrective and preventative actions. monitoring of the networks portfolio of multi-site cancer clinical trials. Using their knowledge of clinical research, they provide technical expertise and overall guidance for the network's quality assurance program. The CRA and Quality Specialist also participates in the development of the networks processes and policies with a focus towards sustainability and growth.
A successful applicant will be highly organized, able to oversee multiple projects in various stages of development, and work collaboratively with a wide variety of internal and external stakeholders.
RESPONSIBILITIES:
Quality Assurance Study Monitoring 70%
Perform on-site and remote monitoring for MNCCTN managed portfolio of multi-site cancer clinical trials in accordance with the QA and study specific monitoring and data management plan. Includes review of participant consent, study participant medical record, EDC, source documentation, regulatory documentation, and pharmacy accountability.
Responsible for monitoring to the standards of the FDA Code of Federal Regulations, ICH GCP guidelines, NIH, the Human Subjects Protection Program and applicable HIPAA regulations.
Evaluate risk levels and analyze compliance trends as defined by the MNCCTN Quality Assurance Plan.
Evaluates site responses to findings and ensures that appropriate corrective actions are completed. Reviews findings for continued compliance concerns and escalates as needed.
Responsible for scheduling and performing study start-up, interim and closeout visits.
Communicates all queries and concerns to both the principal investigator and the research staff and provides training (e.g. Good Clinical Practices, the need for documentation of study procedures, how to obtain informed consent, etc.) when necessary.
Generates visits and close out reports in a timely manner.
Portfolio Team Operations 15%
Participate in study review activities to assess protocols for multi-site implementation appropriateness and success.
Lead / co-lead network calls, meetings, and training initiatives to provide both study-specific and general best practice guidance on QA topics and findings to site staff and study team members.
Lead and collaborate on quality and regulatory reporting efforts for internal and external partners. Prepare data requests for internal and external partners, analyze incoming data for completeness and consistency. Produce quarterly reports and ad hoc reports based on latest data and disseminate as appropriate.
Audit and verify the completeness and accuracy of study documentation, templates, version control in OnCore and Florence eBinders.
Quality Assurance Leadership and Strategic Roadmap - 10%
Accomplish quality assurance program goals in collaboration with MNCCTN Leadership.
Develop, execute, and maintain the MNCCTN Quality Assurance plan and associated guidance documents and procedures.
Serve as an ambassador for MNCCTN quality assurance program.
Participant in training and onboarding of new research staff and provide ongoing mentorship for current portfolio and network staff.
Lead quality assurance educational events for MNCCTN staff and partner sites.
Professional Development 5%
Remain informed of emerging quality assurance standards at the state and federal level including relevant clinical research regulations and guidelines
Engage in professional development opportunities in relevant technologies and best practices