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.
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.
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.