Performs statistical programming and analysis of clinical trial data to support study reports and regulatory submissions.
Collaborates with CROs to validate statistical outputs, ensure accuracy, and resolve data analysis issues.
Develops and maintains SAS macros and safety databases while providing statistical input for SAPs and publications.
Immunovant is a clinical-stage biopharmaceutical company developing FcRn inhibitor therapies for autoimmune diseases. It operates in a dynamic, interactive, fast-paced, and entrepreneurial environment.
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.
Transform real-world, clinical, and preclinical data into reproducible datasets and analyses.
Provide biostatistical support for study design, analysis planning, and statistical programming across the product lifecycle.
Collaborate with cross-functional teams and communicate analytical insights to technical and nontechnical stakeholders.
Calyxo, Inc. is a medical device company focused on transforming kidney stone treatment with innovative devices. Founded in 2016, the company offers a dynamic, diverse, and collaborative culture led by experienced executives and investors.
Develop SAS programs to create clinical trial datasets and outputs.
Ensure compliance with CDISC, FDA, and regulatory standards.
Collaborate with biostatisticians and data managers to support trial reporting.
Penumbra is a global healthcare company focused on innovative therapies for challenging medical conditions. Its collaborative environment emphasizes continuous learning and rewards performance.
Lead and oversee statistical programming activities for oncology clinical trials.
Develop, validate, and maintain SDTM and ADaM datasets in compliance with CDISC standards.
Program and review complex TFLs for clinical study reports and regulatory submissions.
ClinChoice is a global full-service CRO specializing in clinical development and functional solutions for pharmaceutical, biotechnology, medical device, and consumer health companies. They have over 4,000 professionals in more than 20 countries and a culture focused on quality, professional development, and supportive culture.
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.
Deliver accurate, high-quality statistical programming outputs across the clinical trial lifecycle.
Develop and validate SDTM/ADaM datasets, tables, listings, and figures in accordance with CDISC standards.
Support regulatory submissions and collaborate with cross-functional teams to ensure data integrity and compliance.
A partner biotechnology company advancing innovative therapies through clinical development. They foster a collaborative, quality-focused environment with cross-functional teams and external partners.
Lead biostatistical activities for oncology clinical development programs, including study design and analysis strategies.
Collaborate with clinical development, regulatory, and programming teams to ensure high-quality evidence for submissions.
Apply advanced statistical methods, including Bayesian approaches, to support robust trial design and decision-making.
They are a biotechnology company developing innovative cancer therapies, including radiopharmaceutical treatments. The culture emphasizes scientific rigor, collaboration, and meaningful impact in a highly regulated environment.
Provide statistical programming support across oncology programs.
Oversee and review the quality of CRO programming deliverables.
Create, review, and validate SDTM, ADaM, and TFLs.
Vir Biotechnology is a clinical-stage biopharmaceutical company focused on powering the immune system to transform lives by developing medicines for serious infectious diseases and cancer. The company emphasizes a supportive, collaborative culture where colleagues' success drives its mission.
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.
Support statistical analyses of oncology endpoints, including time-to-event and response-based endpoints.
Review SDTM and ADaM specifications, statistical analysis plans, and study documentation while validating statistical outputs.
Collaborate with study teams to conduct routine data review and ensure quality and reproducibility of statistical 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, the company fosters a quality-driven 'one-team' culture that values continuous training and has below industry average turnover rates.
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 strategic leadership and operational oversight for clinical trial design, analysis, and reporting.
Build and mentor a high-performing clinical biostatistics team while driving regulatory submissions.
Partner with cross-functional teams and vendors to ensure high-quality statistical and data management support.
Enveda is a clinical-stage, AI-enabled biotech discovering medicines from nature four times faster than industry standard. With over $845M in total funding and a $2B valuation, the company is recognized as a top startup employer and has three oral medicines in the clinic.
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.
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.
Plan and execute development experiments for Freenome's multiomics cancer screening tests.
Partner cross-functionally with computational, development, regulatory, and quality teams to develop a regulated strategy toward FDA approval.
Use quantitative skills to develop computational methods and interpret complex experimental results to optimize and validate innovative technology.
Freenome is a biotechnology company developing early, noninvasive blood-based tests for cancer detection. The company emphasizes a highly collaborative, cross-functional environment and values diversity.
Lead clinical and economic evidence strategy for Hello Heart's AI and hardware products.
Drive peer-reviewed publications and client-facing evidence with cross-functional partners.
Apply advanced statistics to clinical, claims, and EHR data for executive audiences.
Hello Heart is an AI company focused exclusively on heart health, building a platform that predicts and prevents cardiac events. The company serves over 80% of large U.S. health plans and hundreds of employers, with a positive, diverse, and supportive culture.
Analyze high-throughput DNA sequencing datasets using cancer biology and genomics expertise.
Implement and validate novel algorithms and statistical methods for cancer recurrence monitoring.
Collaborate with molecular biologists and bioinformatics scientists to answer key biological questions.
Natera is a global leader in cell-free DNA testing, dedicated to oncology, women's health, and organ health. The team includes highly dedicated scientists, engineers, and business professionals from world-class institutions who care deeply about their work and each other.