Provide statistical expertise and hands-on support for Phase III oncology clinical trials, including study design and analysis.
Author and review TFL and ADaM specifications, collaborating closely with Statistical Programming.
Manage deliverables across multiple concurrent clinical studies, ensuring timelines and quality expectations are met.
ClinChoice is a global full-service CRO supporting pharmaceutical, biotechnology, medical device, and consumer health companies in clinical development. With over 4,000 professionals in more than 20 countries, they emphasize a quality-driven 'one-team' culture and below-industry-average turnover.
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.
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.
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.
Lead statistician for clinical studies, responsible for study design, analysis, and documentation.
Collaborate with cross-functional teams and manage external vendor work.
Provide statistical expertise for regulatory submissions and act as subject matter expert.
Jazz Pharmaceuticals is a global biopharma company developing life-changing medicines for serious diseases, focusing on oncology and neuroscience. With employees in multiple countries, it fosters a patient-focused, science-driven 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.
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.
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 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.
Perform lead biostatistician role providing technical expertise for complex clinical studies.
Develop statistical sections of protocols, analysis plans, and review tables/figures for regulatory submissions.
Partner with statistical programmers to manage timelines and ensure quality deliverables.
Freenome is developing in vitro diagnostic products for early cancer detection through blood tests. The company values diversity and fosters a collaborative, fast-paced culture.
Develop and validate SAS and R programs to produce CDISC-compliant datasets and TLFs for clinical studies.
Serve as lead programmer on late-phase studies and regulatory submissions, ensuring high-quality, audit-ready deliverables.
Collaborate with cross-functional teams and mentor junior programmers to support statistical programming standards.
Pulmovant is a clinical-stage biotechnology company developing treatments for pulmonary diseases, including its lead candidate mosliciguat for PH-ILD. As part of the Roivant family, it emphasizes collaboration and innovation in advancing its pipeline.
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.
Provide statistical programming support for clinical trials and produce analyses, including generating and validating SDTM/ADaM datasets, tables, listings, and figures.
Work under the direction of senior programmers to review Statistical Analysis Plans and apply appropriate statistical methods.
Assist in developing SAS macros, participate in validation and quality control, and collaborate with cross-functional teams.
Ora is a full-service ophthalmic drug and device development firm guiding clients through all phases of clinical research. With over 400 employees across the globe, the company values kindness, operational excellence, joy, and scientific rigor.
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.
Serve as study statistician for Phase 1-3 vaccine clinical trials, leading statistical design, analysis, and reporting.
Oversee statistical CROs, develop analysis plans, and ensure regulatory and scientific rigor.
Provide statistical consultation across CVIA programs and represent PATH at scientific meetings.
PATH is a global nonprofit dedicated to achieving health equity, developing and scaling innovative solutions to pressing health challenges. With more than 40 years of experience, PATH fosters a culture of collaboration and partnership across diverse teams.
Lead full service clinical projects in Oncology, ensuring timelines, budget, and quality.
Serve as primary client liaison and coordinate cross-functional teams across all study stages.
Manage all aspects of clinical trials, including proposal strategy, documentation, and reporting.
Precision for Medicine is a CRO enabling precision medicine through novel clinical trial designs, biomarker and data analytics, and a focus on rare diseases and oncology. We are a supportive, collaborative team that values work life balance and development.