<h3><span style="color: #1f1f1f;"><strong>About the Role</strong></span></h3> <p><span style="color: #1f1f1f;">The <strong>Oncology Trial Navigator</strong> will play a critical role in connecting Signatera patients to life-changing clinical trial opportunities. As a front-line clinical expert, you will be responsible for the end-to-end execution of patient matching workflows—from initial AI-enabled screening to successful enrollment at a clinical trial site.</span></p> <p><span style="color: #1f1f1f;">You will serve as the primary clinical point of contact for external stakeholders, including treating oncologists, principal investigators (PIs), and research coordinators. This role combines deep oncology clinical knowledge with high-touch stakeholder engagement in a fast-scaling, mission-driven environment. You will work closely with the Senior Manager of Oncology Trial Navigation to pilot and refine the navigation service, providing the "on-the-ground" insights necessary to scale this function across the oncology domain.</span></p> <h3><span style="color: #1f1f1f;"><strong>What You’ll Do</strong></span></h3> <p><span style="color: #1f1f1f;"><strong>Physician & Site Engagement</strong></span></p> <ul> <li style="color: #1f1f1f !important;"><span style="color: #1f1f1f;">Conduct high-volume, structured outreach to oncologists, PIs, and research coordinators regarding trial-eligible patients identified through Natera’s platforms.</span></li> <li style="color: #1f1f1f !important;"><span style="color: #1f1f1f;">Act as a clinical consultant to research sites, delivering patient eligibility notifications and facilitating seamless referral workflows.</span></li> <li style="color: #1f1f1f !important;"><span style="color: #1f1f1f;">Track patient progression from initial identification through referral and enrollment, ensuring timely follow-up and resolution of site-level bottlenecks.</span></li> </ul> <p><span style="color: #1f1f1f;"><strong>Trial Matching & Medical Review</strong></span></p> <ul> <li style="color: #1f1f1f !important;"><span style="color: #1f1f1f;">Operationalize outputs from Natera’s AI-enabled trial matching platform to manage a daily priority queue of potential matches.</span></li> <li style="color: #1f1f1f !important;"><span style="color: #1f1f1f;">Perform rigorous clinical reviews, reconciling patient molecular data (e.g., MRD status, biomarkers) and exome results with trial-specific inclusion/exclusion criteria.</span></li> <li style="color: #1f1f1f !important;"><span style="color: #1f1f1f;">Collaborate with the Clinical Product team to provide real-time feedback on matching accuracy, helping to refine AI algorithms and data filters.</span></li> </ul> <p><span style="color: #1f1f1f;"><strong>Patient & Caregiver Support (as applicable)</strong></span></p> <ul> <li style="color: #1f1f1f !important;"><span style="color: #1f1f1f;">Provide high-level, empathetic, and compliant education to patients regarding specific clinical trial opportunities and the clinical significance of their molecular results.</span></li> <li style="color: #1f1f1f !important;"><span style="color: #1f1f1f;">Coordinate warm handoffs to site research teams, ensuring patients feel supported and informed throughout the referral process.</span></li> </ul> <p> </p> <p><span style="color: #1f1f1f;"><strong>Operational Excellence</strong></span></p> <ul> <li style="color: #1f1f1f !important;"><span style="color: #1f1f1f;">Maintain meticulous documentation of all outreach and referral activities within CRM and tracking tools.</span></li> <li style="color: #1f1f1f !important;"><span style="color: #1f1f1f;">Contribute to the continuous improvement of Standard Operating Procedures (SOPs).</span></li> <li style="color: #1f1f1f !important;"><span style="color: #1f1f1f;">Participate in cross-functional collaboration with internal partners to optimize the field.</span></li> </ul> <p> </p> <h3><span style="color: #1f1f1f;"><strong>Qualifications</strong></span></h3> <p><span style="color: #1f1f1f;"><strong>Education & Licensure:</strong></span></p> <ul> <li><span style="color: #1f1f1f;">Current, active licensure as a <strong>Registered Nurse (RN), Certified Genetic Counselor (CGC), Nurse Practitioner (NP), or Physician Assistant (PA)</strong>.</span> <ul> <li style="color: #000000 !important;"><span style="color: #1f1f1f;">Must maintain licensure in good standing throughout employment.</span></li> <li style="color: #000000 !important;"><span style="color: #1f1f1f;">Board Certification (e.g., OCN, CCRC, or similar) is highly preferred.</span></li> </ul> </li> <li style="color: #1f1f1f !important;"><span style="color: #1f1f1f;">A master’s degree in a clinical or scientific field is preferred.</span></li> </ul> <p><span style="color: #1f1f1f;"><strong>Professional Experience:</strong></span></p> <ul> <li style="color: #1f1f1f !important;"><span style="color: #1f1f1f;">3–5 years of oncology clinical experience, with at least 2 years specifically in <strong>oncology clinical research</strong> (e.g., as a Research Nurse, Coordinator, or