About Us
Our mission is to cure cancer through high performance, accessible early cancer detection. That means saving lives.
Delfi Diagnostics is a Johns Hopkins spinoff focused on the non-invasive detection of cancer at earlier stages, when it is most curable. DELFI uses artificial intelligence and whole-genome sequencing to detect unique patterns of DNA fragmentation in the blood of patients with cancer. These analyses are performed through simultaneous examination of millions of DNA sequences using machine learning to identify tumor-specific abnormalities.
In our passionate pursuit to radically improve health outcomes, we serve humanity when we:
Lead with Science, Anchor in Pragmatism: We pioneer life-changing science by ensuring quality, transparency, and rigor at all times.
Build With & For All: We embrace diverse backgrounds to innovate and achieve together. We are not just building a product—we aim to disrupt the path of cancer for all, no matter geography or socioeconomic class.
Put We over I: We are a home for high-performing people. Through teamwork, we build collective intelligence. Each of us wins when those we serve and those who serve with us win. We show up with empathy, humility, and integrity at every step of the journey.
About the Role
The VP, Clinical Development and Trial Innovation provides strategic leadership across DELFI’s clinical study portfolio, working closely with executive leadership and cross-functional teams including R&D, medical, quality, and regulatory. This leader defines and shapes the comprehensive strategy for all DELFI clinical studies while executing on our key trials supporting product development, launch, and reimbursement. We seek an adaptable, rigorous, future-thinking, and decisive leader who is solidly grounded in clinical development and will champion the use of AI to innovate on clinical trial efficiency. The role requires technical expertise in clinical study design and development, oncology, and preferably diagnostics product development.
What You'll Do
Clinical Study Design & DevelopmentDesign, develop, and execute clinical studies that generate robust evidence for DELFI's current and future pipeline of product claims, including studies that establish clinical validity and clinical utilityAdvance DELFI’s development of diagnostic products for cancer, with the detection of lung cancer in USPSTF-eligible individuals as the first indicationEstablish and implement a comprehensive five-year clinical development strategy based on the latest clinical science, evidence gaps, and unmet needs in cancer diagnosticsPartner with R&D Biostatistics to design case-control and prospective clinical studies, and to analyze those studies in accordance with statistical analysis plansManage the clinical development & clinical operations groups and affiliated CROs, including vendor selection/management/monitoring, site selection, patient enrollment and follow-up, etc.Develop and manage clinical trial timelines, budget, and risks in accordance with overall product development processes and plansRegulatory & Evidence ManagementInteract with FDA on submissions for IVD product approval, including face-to-face/virtual meetings and written presubmissions in coordination with Regulatory AffairsAuthor relevant sections of IVD documents pertaining to clinical development activities, design controls, requirements, etc.Work closely with Medical Affairs to identify evidence gaps and generate real-world data for DELFI's product(s)AI-Enabled Trial Innovation and Product DevelopmentLiaise with the head of R&D and the PIs of research & clinical studies sponsored by DELFI to develop sub-studies and relevant aims that advance DELFI’s R&D pipelineChampion the use of AI to innovate on clinical trial recruitment or efficiencyWork with digital health providers in the US, EU, and Asia to streamline and accelerate trial data collection and scale the cross-referencing of longitudinal clinical and genomic data with national disease registries, health-promotion programs, and socioeconomic and environmental recordsCollaborate with Data Engineering to store, curate, and cross-reference DELFI's clinical dataCommunication, Thought Leadership, and OutreachParticipate in industry stakeholder groups and consortia such as BLOODPAC or the Global Alliance for Genomics and HealthPresent to senior leadership, board of directors, company-wide, and at key national and international scientific & clinical meetings
What You’ll Bring to DELFI
PhD in the physical or natural sciences, or MD. Disciplinary expertise in cancer biology strongly preferred10+ years’ expertise leading the design & development of clinical studies for either pharmaceutical or diagnostics development, as evidenced by strong publication record or successful product releases3-5 years’ experience in IVD diagnostics developmentKnowledge of relevant clinical & regulatory standards such as ICH E6(R3) GCP, ISO 14155, ISO 13485, 21 CFR part 820Familiarity with cutting-edge AI approaches in clinical trials (NLP or LLM for EHRs, digital twins, digital pathology) as well as international data standards such as FAIR principles, FHIR-OMOP, or Common Data Models10+ years’ management experience including best practices in recruiting, coaching, performance management, and career developmentSuperb communication skills including mastery in written & oral presentations, large- and small-group forumsStart-up mindset: passionate, innovative, accountable, able to rapidly prioritize and triage, biased to actionProactive, decisive, and composed with a balance of high IQ & EQ