← Search all jobs

Principal Biostatistician

Brio

Remote (US) · Posted October 10, 2026

Just laid off? Start here: a plan for the first weeks

See every open role at Brio

More in Pharmaceuticals & Biotech · Data & Analytics jobs

Similar jobs

Data & Analytics jobs in the rankings

How AI is used in this kind of work

Among statisticians, AI is already used for some of the tasks. Measured exposure for statisticians: 21% (some).

Share of this job’s tasks that AI is already used for at work, from real usage. It is not a forecast of job loss, and a low number means no use seen yet. Source: Anthropic Economic Index.

Check how this applies to your own job

Skills this job asks for

Say which you have and which you want to build. We use it to match you to jobs like this one.

About the job

BACK TO JOBS Principal Biostatistician APPLY NOW Job Title : Principal Biostatistician Company : Biopharma Location : Remote Brio Resource Group is a Life Sciences Executive Search Firm committed to providing rare talent on an exclusive search basis to the Biopharma, Pharma, Device and CRO industries. We work on behalf of organizations that value true talent acquisition partners and specialize in supporting emerging Biopharma companies offering life-changing therapies. Our many years of experience, subject matter expertise, comprehensive search process and genuine passion to deliver rare talent defines Brio. Position Overview : ​As a Principal Biostatistician, you will be responsible for statistical support regarding clinical studies and providing crucial statistical outputs for regulatory submissions. Opportunity Highlights : Contribute as a statistician to studies and project teams Provide statistical insights across clinical development phases Shape statistical aspects of trial outcomes and reporting Develop strategies for program-level statistical analysis Ensure quality and adherence in statistical processes and data management Position Requirements : Master’s Degree required 5+ years of experience in clinical trial within the pharmaceutical industry Proficiency in SAS and another statistical programming language Expertise in CDISC requirements for regulatory submissions, including STDM, ADaM, and SEND data standards Familiarity with DA, EMA, and ICH drug development guidelines Skillful presentation of statistical concepts to clinical teams We welcome the opportunity to provide a full job description upon resume review. How to Apply: In order to be considered for the above opportunity, simply apply via LinkedIn and include your CV. We respond to applicants who meet our position requirements, but suggest submitting your resume for future consideration for our expanding list of new opportunities surfacing daily within our Biopharma network. We have a strict honor code at Brio respecting your confidentiality and we only share your information with your consent. Brio Resource Group, LLC considers all applicants without regard to race, color, religion, sex, national origin, age, mental or physical disabilities, or any other similarly protected status.