• Serve as the CQA Lead for clinical programs. • Set the vision for clinical compliance and ensure quality is integrated into study design and execution. • Provide expert interpretation of FDA, ICH-GCP, EMA, and other regulatory requirements. • Monitor the evolving regulatory landscape to ensure compliance and 'inspection-ready' operations. • Qualify and manage clinical vendors (CROs, central labs) and oversee a risk-based site audit schedule. • Serve as the primary point of contact for regulatory inspections. • Provide strategic guidance on the investigation of significant quality events. • Review and approve CAPA plans for effective remediation of systemic GCP issues. • Review and provide final Quality approval for key clinical documents. • Provide CQA performance metrics and trend analysis for Quality Management Reviews. • Lead GCP training initiatives for clinical operations and cross-functional partners.

About Radformation Radformation is transforming the way cancer clinics deliver care. Our innovative software automates and standardizes radiation oncology workflows, enabling clinicians to plan and deliver treatments faster, safer, and more consistently, so patients everywhere can receive the same high-quality care. Our software focuses on three key areas: - Time savings through automation. - Error reduction through automated systems. - Increased quality care through advanced algorithms and workflows. We are a fully remote, mission-driven team united by a shared goal: to reduce cancer’s global impact and help save more of the 10 million lives it claims each year. Every line of code, every product release, and every conversation with our customers brings us closer to ensuring no patient’s treatment quality depends on where they live. Why This Role Matters In this role, you will help advance treatment accuracy and efficiency by supporting Radformation’s adaptive radiation therapy product through rigorous quality assurance and validation. You will work closely with the Product Manager, engineering team, Success, Support, and Regulatory teams to ensure product quality, troubleshoot issues, and support the successful delivery of adaptive solutions to clinics. Responsibilities Include: - Testing new product versions prior to release to ensure quality and functionality - Performing verification and validation testing to maintain product integrity - Coordinating with Success and Support teams to troubleshoot issues and assist with clinic setup - Providing feedback to Product and Engineering teams to improve product performance and usability - Generating documentation for product-related materials and medical device requirements - Supporting Medical Device documentation in collaboration with Regulatory, including defining requirements, outlining testing conditions, executing and documenting testing, and mitigating software risks Required Experience: - 5+ years experience as a clinical medical physicist - 5+ years of in-clinic experience with online adaptive system(s) - Direct treatment planning experience, specifically related to online adaptive - Experience with implementation of AAPM Task Group reports related to online adaptive programs, contouring, and image registration Preferred Experience: - 5+ years experience as a clinical medical physicist using Radformation products - Experience with multiple online adaptive systems - Direct experience planning with multiple treatment planning systems - Experience with verification and/or validation testing - Experience using Visual Studio or similar coding software - Programming experience using C# - Customer service experience AI & Hiring Integrity At Radformation we believe AI can be an incredible tool for innovation, but our hiring process is all about getting to know you, your skills, experience, and unique approach to problem solving. We ask that all interviews and assessments be completed without tools that generate answers in real time. This helps ensure a fair process for everyone and allows us to see your authentic work. Using such tools during the process may affect your candidacy. Benefits & Perks — What Makes Us RAD We care about our people as much as we care about our mission. We offer competitive compensation, benefits, and the opportunity to make an impact in the fight against cancer. The salary range for this role is $150,000 – $200,000 USD base plus bonus eligibility. For US teammates (via TriNet): Health & Wellness - Multiple high-quality medical plan options with substantial employer contributions toward premiums, often covering the full cost depending on the plan selected. - Health coverage starting on day one - Short-term and long-term disability and supplementary life insurance Financial & Professional Growth - 401(k) with employer match vested immediately - Annual reimbursement for professional memberships - Conference attendance and continued learning opportunities Work-Life Balance & Perks - Self-managed PTO and 10 paid holidays - Monthly internet stipend - Company-issued laptop and one-time home office setup stipend - Fully remote work environment with virtual events and yearly retreats, because we like to have fun while doing work that matters For global teammates (via Deel):At Radformation, we want every team member to feel supported, no matter where they live. For teammates outside the US, we provide benefits that align with local laws and standards, working with our Employer of Record (EOR) partners to ensure fairness and equity. This means your benefits package will be locally compliant, competitive, and designed to support your health, financial security, and work-life balance. Our Commitment to Diversity Cancer affects people from every walk of life, and we believe our team should reflect that diversity. Radformation is proud to be an equal opportunity workplace and an affirmative action employer. We welcome candidates from all backgrounds and are committed to fostering an inclusive environment for all employees. Agency & Candidate Safety Notice Radformation does not accept unsolicited resumes from agencies without a signed agreement in place. We do not partner with third-party recruiters unless explicitly stated. All legitimate communication from Radformation will come from an @radformation.com email address. If you receive outreach from another domain or via unofficial channels, please contact careers@radformation.com.

• Review all assigned OASIS assessments (SOC, ROC, Recert, Transfer, Discharge) for accuracy, completeness, and internal consistency. • Proper clinical coding and scoring. • Validation of diagnosis coding and sequencing per CMS guidelines. • Provide clear, actionable feedback to clinicians when revisions are required. • Ensure OASIS submissions meet current CMS, Medicare, and payer requirements. • Identify recurring documentation trends or risk areas and contribute recommendations for improvement.

• Writing and executing test cases to verify the functionality of software • Analyzing the functionality of applications and designing automated tests • Work closely with legal and engineering teams to ensure the quality of services • Create detailed, comprehensive, and well-structured test scenarios and test cases • Prioritize, plan and coordinate testing activities • Identify and unearth issues in the early stage of development • Create and maintain test artifacts • Perform thorough regression testing when issues are resolved