Lead statistical strategy across multiple complex clinical, diagnostic, and evidence-generation studies.
Serve as a senior statistical expert to clinical, scientific, regulatory, and product stakeholders.
Mentor statisticians, establish analytical best practices, and influence study design and regulatory responses.
Karius is a venture-backed clinical metagenomics company that uses genomics and AI to detect microbial cell-free DNA in blood, helping physicians diagnose infectious diseases. The company is committed to advancing diagnostic science and fostering a diverse, inclusive workplace.
Lead privacy impact assessments, regulatory analyses, and risk-based recommendations balancing compliance with business enablement.
Embed privacy-by-design into product and software development lifecycles, partnering with engineering to make privacy practical and scalable.
Operationalize guardrails for sensitive data, AI/ML training data, and advanced analytics, and govern data flows across commercial and clinical ecosystems.
Natera is a global leader in cell-free DNA (cfDNA) testing, dedicated to oncology, women's health, and organ health. Our team consists of highly dedicated professionals from world-class institutions who care deeply for our work and each other.
Own statistical strategy across the portfolio while staying hands-on as lead statistician on live programmes.
Serve as primary statistical interface with regulators and assess in-licensing assets' statistical rigour during due diligence.
Build and lead the biostatistics, statistical programming, and medical writing functions as the team grows.
Lindus Therapeutics is building the next generation of biopharma by in-licensing clinical-stage assets and developing them through Lindus Health's technology-first clinical trial infrastructure. It is a new, small team with a proven foundation of 40+ completed trials.
Provide statistical leadership for oncology clinical development programs, including Phase I–III trials and regulatory submissions.
Lead development of SAPs, sample size calculations, randomization strategies, and ensure quality of statistical deliverables.
Collaborate with cross-functional teams, serve as statistical SME, and mentor junior biostatisticians.
ClinChoice is a global full-service CRO delivering clinical development and functional solutions for pharmaceutical, biotechnology, and medical device companies. With over 4,000 professionals in 20+ countries, we are committed to high-quality delivery, continuous training, and a diverse, inclusive culture.
Provide statistical leadership across clinical development programs from early-phase through late-phase trials.
Lead clinical trial design, develop SAPs, and oversee statistical analyses for regulatory submissions.
Collaborate with cross-functional teams and mentor statisticians to ensure scientific rigor and regulatory compliance.
ClinChoice is a global full-service CRO providing clinical development and functional solutions for pharmaceutical, biotechnology, medical device, and consumer health companies. With over 4,000 professionals in more than 20 countries, it fosters a quality-driven 'one-team' culture focused on continuous training and diversity.
Develop statistical models and machine learning algorithms to improve patient enrollment and trial management.
Build and optimize data pipelines and analytical workflows using AWS tools like Athena, Redshift, SageMaker, and dbt.
Ensure data science practices comply with HIPAA and GDPR while monitoring models for bias and performance drift.
Care Access brings clinical research and health services to communities worldwide through hundreds of research locations and mobile clinics. The company is dedicated to making healthcare more accessible and puts people at the heart of medical progress.
Provide statistical support across all phases of clinical development, including protocol design, analysis plans, and complex study methodologies.
Author and review statistical analysis plans, generate analysis datasets, tables, and figures using SAS, and perform quality control for statistical programs.
Act as a biostatistical consultant to sponsors and internal teams, overseeing study timelines, budgets, and regulatory interactions.
Precision Medicine Group is a precision medicine company providing comprehensive clinical development and biostatistics services. They are a global, equal opportunity employer with a collaborative and service-oriented culture.
Operationalize enterprise privacy governance frameworks to enable responsible, compliant, and scalable use of information.
Partner with Legal, Regulatory, Security, and AI governance teams to embed privacy-by-design into products and platforms.
Provide privacy guidance across clinical research, secondary data use, genomics, and precision medicine initiatives.
Natera is a global leader in cell-free DNA testing, dedicated to oncology, women's health, and organ health. The company brings together highly dedicated professionals from world-class institutions, fostering a culture that values solving complex problems, empowering others, and leading by example.
Lead statistical programming activities across multiple studies, ensuring quality and timely delivery.
Develop and validate TLFs, SDTM/ADaM datasets, Define-XML, and SAS programs.
Provide technical oversight, mentoring, and collaboration with cross-functional teams.
ClinChoice is a global full-service CRO providing clinical development and functional solutions for pharma, biotech, medical device, and consumer health companies. With over 4,000 professionals across 20+ countries, they value continuous training, diversity, and inclusion.
Manage and maintain Virta's privacy compliance program, including policies, procedures, PIAs, and records of processing activities.
Act as primary point of contact for privacy inquiries from customers, prospects, and partners, supporting DPAs, BAAs, RFPs, and due diligence.
Drive cross-functional privacy initiatives, training, metrics, and incident response workflows to strengthen Virta's privacy posture.
Virta Health is on a mission to reverse metabolic disease in one billion people through virtual care, personalized nutrition, and technology. Backed by over $350 million from top-tier investors, the remote-first company partners with health plans and employers to help members restore their health.
Provide strategic statistical leadership across oncology development programs, collaborating with Clinical Development, Regulatory, Medical, Commercial, and Portfolio teams.
Design and validate trial types, endpoints, and innovative adaptive designs while performing sample size/power calculations and establishing go/no-go decision gates.
Support regulatory submissions and health authority interactions, and quantify technical success probability for pipeline prioritization.
We are a global full-service CRO specializing in clinical development and functional solutions for pharmaceutical, biotechnology, medical device, and consumer health companies. With over 4,000 professionals in more than 20 countries, we are committed to training, diversity, and accelerating innovative drug and device development.
Lead statistical programming activities for Gene Therapy clinical trials from start-up through database lock, analysis, and reporting.
Develop, review, and validate SAS programs for SDTM, ADaM, Tables, Listings, and Figures in compliance with CDISC standards.
Collaborate with Biostatisticians and cross-functional teams to support regulatory submissions and manage study-level deliverables.
ClinChoice is a global full-service CRO specializing in clinical development and functional solutions for pharmaceutical, biotechnology, medical device, and consumer health companies. With over 4,000 professionals in more than 20 countries, we offer a supportive culture, continuous training, and a strong commitment to diversity and inclusivity.
Lead statistical programming activities for clinical trials, collaborating with statisticians and data management teams.
Design, create, and validate SDTM and ADaM datasets, ensuring traceability and CDISC compliance.
Develop and validate Tables, Listings, and Figures using SAS for clinical study reports and regulatory submissions.
Kyverna Therapeutics is a patient-centered, clinical-stage biopharmaceutical company developing cell therapies for patients suffering from autoimmune diseases. Guided by core values of collaboration and innovation, the company is committed to transforming the future of treatment for autoimmune disease.