Associate Director, Computational Development

🕒 Abril 6

🏄 California – Remoto

🏄 California – Remote

💵 $192.000 - $208.000 / ano

⏰ Tempo Integral

🟠 Sênior

👔 Diretor

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Veracyte, Inc.

SiteLinkedInTodas as Vagas

501 - 1000 funcionários

Fundada em 2013

🧬 Biotecnologia

⚕️ Seguro de Saúde

💊 Farmacêutico

Biotechnology • Healthcare Insurance • Pharmaceuticals

A Veracyte, Inc. é uma empresa de diagnósticos genômicos que se concentra em capacitar os clínicos com testes moleculares de alto valor para o diagnóstico e tratamento do câncer. A empresa oferece um portfólio de classificadores genômicos para vários tipos de câncer, incluindo câncer de tireoide, próstata, pulmão, mama e bexiga, bem como doença pulmonar intersticial. Os testes da Veracyte ajudam clínicos e pacientes a tomar decisões informadas sobre o cuidado com o câncer, fornecendo insights diagnósticos e prognósticos claros. A abordagem da empresa envolve identificar necessidades clínicas não atendidas e desenvolver testes de alto desempenho que são amplamente acessíveis globalmente através de um modelo baseado em CLIA e diagnóstico in vitro. Comprometida em elevar o padrão do cuidado com o câncer, a Veracyte continua a expandir seu portfólio de testes e a fazer contribuições significativas na área de diagnósticos oncológicos.

Descrição

• Provide bioinformatics leadership for MRD assay design, development, and optimization across one or more LDT programs, ensuring alignment with scientific, clinical, and business objectives. • Serve as a senior scientific contributor and reviewer for assay concepts, signal detection strategies, error suppression approaches, and MRD calling methodologies. • Apply deep expertise in cancer genomics, ctDNA biology, and NGS technologies to guide assay architecture and analytical decision‑making. • Lead and/or oversee analytical study design and data analysis for assay development and validation, including accuracy, limit of detection, precision, and robustness. • Guide development, validation, and maintenance of scalable, production‑ready bioinformatics pipelines supporting MRD analysis, QC, and reporting. • Review and approve analytical approaches, benchmarking studies, and optimization strategies, ensuring scientific rigor and regulatory readiness. • Ensure compliance with standards (CAP/CLIA, FDA, IVDR) throughout the bioinformatics development lifecycle, including rigorous testing and documentation. • Provide day‑to‑day scientific mentorship and technical guidance to bioinformatics scientists and senior scientists. • Support career development of team members through coaching, technical review, and knowledge sharing. • Communicate complex analytical concepts clearly to stakeholders at varying levels of technical depth, including senior leadership.

🎯 Requisitos

• Ph.D. in Bioinformatics, Computational Biology, Genomics, Biostatistics, or a closely related quantitative field. • Minimum 8 years of total relevant experience, with at least 5 years of management experience in biotech, diagnostics, or regulated healthcare environments. • Demonstrated experience leading NGS‑based assay development for clinical diagnostics. Hands‑on experience with ctDNA‑based MRD assays, including personalized or tumor‑informed approaches. • Strong programming skills in Python, with experience developing and benchmarking reproducible, production‑grade analysis pipelines, including experience with SDLC best practices. • Proven experience working in design‑controlled, regulated environments (CAP/CLIA LDT, IVD, or equivalent) is a must. • Track record of working with wet lab scientists on iterative experiment design, execution, analysis, and interpretation as a tightly integrated team. • Demonstrated record of technical and scientific leadership, ownership, and independent work.

🏖️ Benefícios

• Health insurance • Competitive compensation • Professional development opportunities • Flexible work arrangements • Inclusion in a diverse workforce