Lead the statistical design and analytical planning for oncology clinical utility studies with innovative methodologies.
Author and review high-quality statistical deliverables including SAPs and reports for cross-functional collaborators.
Mentor early career statisticians and support continuous improvement of departmental processes and tools.
Natera is a global leader in cell-free DNA testing, dedicated to oncology, women's health, and organ health. The team consists of highly dedicated professionals from world-class institutions, working in a fast-paced environment.
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.
Lead biostatistics activities across clinical studies, ensuring high-quality analyses and clear communication.
Provide statistical expertise for oncology trials, from protocol development to regulatory submissions.
Oversee statistical programming and deliverables, ensuring quality, integrity, and compliance.
Jobgether is a platform that uses AI-powered matching to connect candidates with hiring companies, focusing on objective and fair application reviews. The company is dynamic and emphasizes a streamlined hiring process, with a data-driven approach and a commitment to innovation.
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.
Support development and validation of datasets, tables, figures, and listings for clinical trials using SAS and/or R.
Assist with CDISC-compliant SDTM and ADaM datasets, Define-XML, and electronic submission deliverables.
Perform programming validation, quality checks, and collaborate with cross-functional teams to meet project timelines.
ClinChoice is a global full-service CRO supporting 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 emphasizes a quality-driven one-team culture and continuous employee training.
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 the identification, development, and application of innovative statistical methodologies for clinical development programs.
Provide expert statistical consultation and shape statistical strategies for clinical trial design and analysis.
Mentor statisticians and build a statistical innovation team to foster methodological excellence.
Alnylam is the leader in RNAi therapeutics, a revolutionary approach with the potential to transform the lives of people with rare and common diseases. The company is a globally recognized top employer with an authentic, inclusive culture and a deep pipeline, late-stage programs, and a bold vision.
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.
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.
Independently lead statistical design and analysis for preclinical studies, including dose-response modeling and aging biomarker studies.
Build and apply population PK/PD models to support internal dose-justification and formulation decisions.
Conduct exploratory analyses to support endpoint development and target/pathway discovery.
Loyal is a clinical-stage veterinary medicine company developing longevity drugs for dogs. Loyal is a well-funded startup with teams of scientists, veterinarians, engineers, operators, and creatives.
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.