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Remote Principal Biostatistician Jobs (NOW HIRING)

Biogen

Sr. Principal Biostatistician

$134K - $179K/yr

As a Senior Principal Biostatistician, you will be at the forefront of leading study design and ... Although we are open to Remote candidates, the strong preference would be to have a Hybrid presence ...

Biogen

Sr. Principal Biostatistician

$134K - $179K/yr

As a Senior Principal Biostatistician, you will be at the forefront of leading study design and ... Although we are open to Remote candidates, the strong preference would be to have a Hybrid presence ...

Cytel

An experienced Principal Biostatistician with a passion for clinical development and analysis, adept at utilizing advanced statistical methods, you will lead one Phase I-IV clinical studies across ...

Geisinger

Biostatistician

Danville, PA · On-site +1

This position has the potential to be remote. Work is typically performed in an office or remote ... Independently provides statistical consultations or collaborations with clinical principal ...

Vrtx

Principal Statistical Programmer

Boston, MA · Remote

$149K - $223K/yr

Engages with a variety of other functions, including Statistical Programmers, Biostatisticians ... Remote-Eligible Flex Eligibility Status: In this Remote-Eligible role, you can choose to be ...

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How much do remote principal biostatistician jobs pay per hour?

As of Sep 12, 2026, the average hourly pay for remote principal biostatistician in the United States is $84.56, according to ZipRecruiter salary data. Most workers in this role earn between $72.84 and $97.60 per hour, depending on experience, location, and employer.

What is a remote principal biostatistician?

A Remote Principal Biostatistician is a senior-level biostatistics professional who analyzes complex medical and clinical trial data while working remotely. They design statistical methodologies, develop study protocols, and ensure data integrity for regulatory submissions. This role often requires collaboration with cross-functional teams, such as data managers and medical writers. Strong expertise in statistical programming (e.g., SAS, R) and regulatory guidelines (e.g., FDA, EMA) is essential. Remote work allows flexibility while maintaining responsibility for high-level statistical oversight and decision-making.

What are the typical daily responsibilities of a remote principal biostatistician?

As a Remote Principal Biostatistician, your daily activities often include designing and overseeing statistical analyses for clinical studies, reviewing protocols and statistical analysis plans, and ensuring adherence to regulatory requirements. You may lead project meetings with cross-functional teams such as data managers, clinical researchers, and programmers, providing statistical expertise and resolving complex methodological issues. Additionally, you are responsible for mentoring junior team members, performing quality control on statistical deliverables, and communicating analysis results to both scientific and non-technical stakeholders. This role relies heavily on self-motivation, organized workflows, and clear virtual communication to ensure high-quality outcomes in a remote environment.

What are the key skills and qualifications needed to thrive in the remote principal biostatistician position?

To thrive as a Remote Principal Biostatistician, you need advanced knowledge of biostatistics, clinical trial design, and statistical data analysis, typically supported by a master's or PhD in statistics, biostatistics, or a related field. Expertise in statistical programming languages such as SAS, R, and experience with clinical data management systems and regulatory guidelines (e.g., ICH/GCP) are essential. Strong leadership, effective communication, and project management skills help you coordinate cross-functional teams and mentor junior statisticians. These competencies ensure high-quality statistical deliverables, regulatory compliance, and successful remote collaboration on complex research projects.

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Remote Principal Biostatistician jobs near you
Infographic showing various Remote Principal Biostatistician job openings in the United States as of September 2026, with employment types broken down into 90% Full Time, 8% Part Time, 1% Temporary, and 1% Contract. Highlights an 91% Physical, 3% Hybrid, and 6% Remote job distribution, with an average salary of $175,884 per year, or $84.6 per hour.

Principal Biostatistician - Medical Affairs (Remote)

Fairfield, CT • On-site, Remote

Penfield Search Partners
Recruiting and Staffing Services • 11 - 50 employees
Learn more about Penfield Search Partnersexternal

Full-time

Re-posted 2 days ago

Job description

Job Description We are partnering with a leading biopharmaceutical client seeking an experienced Principal Biostatistician to support its Medical Affairs Statistics, Epidemiology, and Real-World Evidence (RWE) organization. This individual will perform and validate statistical analyses in support of Medical Affairs initiatives while providing oversight of statistical and programming work conducted by external vendors as needed. The Principal Biostatistician will collaborate closely with cross-functional Medical Affairs stakeholders on evidence-generation activities, including those incorporating real-world data and evidence.

The role will provide statistical guidance on clinical and lifecycle management initiatives, advise on analytical strategies, and recommend appropriate methodological approaches to support integrated evidence generation and informed decision-making. Essential Functions Work collaboratively with other members of the Medical Affairs team to develop and provide scientifically sound analyses that answer questions to support and enhance publications and knowledge of company products. Contribute to publication objectives including timelines, statistical and analytical requirements for publications and projects.

Develop, design, and oversee or perform post-hoc analyses of existing databases and meta-analyses as needed and appropriate Support clinical development biostatistics with exploratory analyses necessary for submissions and regulatory queries. Review publications, marketing materials, and education and training materials that contain clinical data and product claims Stay informed with data being generated in current clinical development programs Manage CROs regarding statistical activities to ensure timely delivery of quality analysis results as necessary Collaborate and provide statistical support to the HEOR group in relevant areas including HTA and NTAP submissions. Develop real world evidence strategies utilizing real-world data assets to design and execute RWE research projects, including the development of protocols and statistical analysis plans, in collaboration with epidemiology and RWE leadership team.

Stay current with new developments in statistics, drug development, and regulatory guidance through literature review, conference attendance, and other professional development activities. Minimum Requirements Master's degree with >2 years of experience; OR PhD in statistics, mathematics or a related discipline with a statistical focus. Proficient in drug development regulations pertinent to statistical analysis Proficient SAS & R programming skills Understanding of CDISC SDTM and ADAM models and standards is preferred, but not required.

Excellent writing and communication skills, demonstrated leadership abilities and excellent interpersonal skills. Able to work in a fast-paced, flexible, team-oriented environment.

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