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Posted 3 hours agoSenior Manager, Oncology Trial Navigation
at Natera
United StatesRemote
Responsibilities
- Deliver patient eligibility notifications and facilitate referral workflows.
Requirements
- ● Operationalize outputs from Natera’s AI-enabled trial matching platform.
- ○ Required to maintain licensure in good standing throughout employment.
- ○ Board Certification (e.g. OCN, CCRC or similar) is highly preferred.
- ● A master's degree in a clinical or scientific field is highly preferred. Professional Experience:
- experience specifically in patient identification and trial matching services at a leading molecular diagnostics laboratory or independent clinical trial matching company. Leadership Experience:
- experience in building and scaling a clinical program.
- ● Demonstrated ability to manage direct reports and mentor team members in a fast paced environment.
- ● Advanced clinical knowledge in oncology with deep understanding of biomarker driven oncology, MRD based clinical trial landscapes
- ● Expert-level understanding of clinical trial design and the ability to interpret complex inclusion/exclusion criteria.
- ● Familiarity with centralized screening or trial referral models.
- Experience communicating with patients, physicians, PIs, and research coordinators.
- Technical & Data Proficiency:
- ● Ability to quickly learn new technologies and serve as primary business stakeholder for technological solutions utilized in Oncology Trial Navigation.
- ● Ability to design, implement, and scale clinical navigation workflows.
- ● High degree of empathy and professionalism in patient-facing interactions.
- Natera™ is a global leader in cell-free DNA (cfDNA) testing, dedicated to oncology, women’s health, and organ health.
Experience
- ● 5+ years of oncology clinical experience, with at least 3 years specifically in oncology clinical research.
Benefits
- The pay range is listed and actual compensation packages are based on a wide array of factors unique to each candidate, including but not limited to skill set, years & depth of experience, certifications and specific office location.
- Remote USA $168,000 — $200,000 USD OUR OPPORTUNITY
- Our aim is to make personalized genetic testing and diagnostics part of the standard of care to protect health and enable earlier and more targeted interventions that lead to longer, healthier lives.
- benefits include comprehensive medical, dental, vision, life and disability plans for eligible employees and their dependents.
- Additionally, Natera employees and their immediate families receive free testing in addition to fertility care benefits. Other
- benefits include pregnancy and baby bonding leave, 401k benefits, commuter
Contact
- For more information, visit www.natera.com .
- Link: https://www.natera.com/notice-of-data-collection-california-residents/
- Please be advised that Natera will reach out to candidates with a @ natera.com email domain ONLY.
Additional details
- The Senior Manager of Oncology Trial Navigation will drive operational scalability and execution of our oncology trial navigation program, playing a critical role in supporting the connection of Signatera patients to appropriate clinical trial opportunities while focusing on strategic program growth and team leadership.
- You will serve as the operational bridge between Natera’s centralized patient screening team and external stakeholders—including treating oncologists, principal investigators (PIs), research coordinators, and, when appropriate, patients themselves.
- You will play a key role in operationalizing and scaling the oncology focused trial navigation program, partnering with internal stakeholders to harmonize best practices, refine clinical workflows, and scale the team’s reach.
- This is a unique opportunity for an experienced clinician to drive strategic development of a function that directly accelerates oncology clinical trial enrollment in a fast-scaling, mission driven environment.
- This role demands exceptional communication and cross functional collaboration to successfully deliver and expand clinical trial support in the oncology domain.
- ● Support site prioritization and activation strategies.
- ● Ensure timely follow-up and outcome tracking.
- ● Support eligibility review by aligning molecular and clinical data with trial inclusion/exclusion criteria.
- ● Track patient progression from identification through referral and enrollment.
- ● Provide high-level, compliant education about trial opportunities.