Source Job

US

  • Provide statistical leadership across clinical research projects, ensuring high-quality methodologies and analyses.
  • Collaborate with cross-functional teams to support innovative study designs and advanced statistical modeling.
  • Author and review Statistical Analysis Plans (SAPs), tables, listings, and figures for regulatory submissions.

Statistical Analysis CDISC SAS Clinical Research Regulatory Submissions

7 jobs similar to Principal Statistician

Jobs ranked by similarity.

India

  • Apply advanced statistical expertise to support impactful clinical research and data-driven decision-making.
  • Lead statistical analysis activities for clinical trial programs, ensuring data accuracy, scientific rigor, and clear reporting.
  • Collaborate with multidisciplinary teams to interpret results, support decision-making, and deliver high-quality statistical outputs.

Jobgether is an AI-powered job matching platform connecting candidates with hiring companies. It uses automated screening to shortlist top-fitting candidates for each role.

$220,700–$272,700/yr
United States

  • Lead product-level biostatistics tasks including regulatory interactions and filings, ensuring statistical integrity.
  • Contribute to study design, sample size determination, and author/review statistical analysis plans and TFL specifications.
  • Mentor junior team members and collaborate cross-functionally to meet product deliverables and timelines.

Ultragenyx is a biopharmaceutical company focused on developing life-changing treatments for rare diseases. The company fosters a supportive, inclusive culture emphasizing learning and growth, enabling employees to thrive professionally and personally.

$275,000–$290,000/yr
US Unlimited PTO

  • Lead the biometrics team including statisticians, data managers, and statistical programmers at a program level, providing strategic input for clinical development.
  • Author and develop Statistical Analysis Plans (SAPs), contribute to trial designs, protocol development, and sample size calculations, and oversee vendor deliverables.
  • Interact with global health authorities, contribute to regulatory submissions, and coordinate statistical analyses for safety updates and ad hoc requests.

Spyre Therapeutics is a clinical-stage biotechnology company developing next-generation long-acting antibodies to redefine the standard of care for inflammatory bowel disease and rheumatic diseases. As a growing company, they offer a fast-paced, dynamic environment where you help shape the culture and contribute broadly to meaningful medicines.

Europe

  • Maintains responsibility for all assigned biostatistics duties within clinical studies, including acting as study lead for multiple or complex studies.
  • Reviews and develops clinical program designs, protocols, and statistical analysis plans, ensuring high-quality and valid content.
  • Provides mentoring to junior statisticians and represents the biostatistics function in internal and external meetings and audits.

Ergomed Group is a rapidly expanding full-service mid-sized CRO specialising in Oncology and Rare Disease. Since 1997, the company has grown organically with operations in Europe, North America and Asia, fostering a true international culture that values employee experience, well-being, and work-life balance.

$110,500–$184,000/yr
Global

  • Provides statistical consulting, study design, and data analysis for clinical trials.
  • Communicates complex statistical concepts to non-statistical stakeholders and clients.
  • Supports business development, thought leadership, and scientific publications.

Alimentiv is a clinical research organization that provides biostatistical and clinical services to pharmaceutical and biotech clients. They have a Statistical Center of Excellence and offer a remote-based role with a focus on innovation and regulatory compliance.

US

  • Lead programming activities for oncology clinical trials, developing and validating SDTM and ADaM datasets following CDISC standards.
  • Oversee production of Tables, Listings, and Figures (TLFs) for study reporting and regulatory submissions.
  • Collaborate with Biostatistics, Data Management, and Regulatory Affairs to ensure compliance with FDA, EMA, and PMDA requirements.

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 28 years of experience, they employ more than 4,000 professionals across 20+ countries, fostering a culture of diversity and continuous training.

US

  • Act as a domain authority establishing benchmarks for AI-driven statistical results.
  • Provide knowledge sharing about day-to-day workflows and regulatory submissions.
  • Identify and correct discrepancies in data quality and generate reference artifacts.

Edison Scientific builds and commercializes AI agents for science. We are assembling a team of top researchers and engineers across AI and biology to build an AI scientist.