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Global Biostatistics Jobs (NOW HIRING)

Maintain alignment across global teams, including effective collaboration with US- and China-based ... Support biostatistics activities across a diverse clinical pipeline, including complex and data ...

Biostatistics Senior Manager What you will do Let's do this. Let's change the world. In this vital ... Global Biostatical Science) through participating in and collaborating with multidisciplinary ...

We are global collaborators who achieve together - researching, manufacturing, and delivering ever ... Biostatistics Sr. Manager What you will do Let's do this. Let's change the world. As a ...

Biostatistics Senior Manager What you will do Let's do this. Let's change the world. In this vital ... Global Biostatical Science) through participating in and collaborating with multidisciplinary ...

The Senior Director Biostatistics will partner with other company leaders to design and implement ... of global regulatory authorities with a high probability of technical success * In collaboration ...

Role Summary As a strategic leader within the Global Biometrics Department, the Director, Biostatistics leads the development and implementation of statistical solutions in clinical trials, evidence ...

Senior Director, Biostatistics

OR ยท On-site +1

$290K/yr

Global Health Authority Interaction: Contribute to documents submitted to Health Authorities ... Build and develop efficient biostatistical processes and standards, when appropriate Ideal ...

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Global Biostatistics information

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How much do global biostatistics jobs pay per hour?

As of Aug 15, 2026, the average hourly pay for global biostatistics in the United States is $57.55, according to ZipRecruiter salary data. Most workers in this role earn between $40.62 and $64.42 per hour, depending on experience, location, and employer.

What is global biostatistics?

Global Biostatistics is a field that involves the application of statistical methods to biological, medical, and public health research on an international scale. Professionals in global biostatistics design, analyze, and interpret data from clinical trials and health studies conducted worldwide. They support drug development, evaluate treatment effectiveness, and help guide regulatory decisions across diverse populations. Global biostatisticians often work with multinational teams and must consider variations in healthcare practices, regulations, and data standards across countries.

What are the key skills and qualifications needed to thrive as a global biostatistician, and why are they important?

To thrive as a Global Biostatistician, you need a strong background in statistics, data analysis, and clinical research, typically supported by a master's or PhD in biostatistics or a related field. Proficiency with statistical software such as SAS, R, or STATA, and familiarity with regulatory guidelines like ICH or FDA standards, are essential. Strong problem-solving abilities, attention to detail, and effective communication skills help set candidates apart in global project environments. These skills ensure accurate data interpretation, regulatory compliance, and effective collaboration in the development of healthcare solutions worldwide.

What is the difference between Global Biostatistics vs Clinical Biostatistics?

AspectGlobal BiostatisticsClinical Biostatistics
Required CredentialsMaster's or PhD in Biostatistics, Statistics, or related fieldMaster's or PhD in Biostatistics, Statistics, or related field
Work EnvironmentInternational projects, multi-country studies, global health organizationsClinical trial sites, hospitals, pharmaceutical companies
Employer & Industry UsageGlobal health agencies, international pharma, NGOsPharmaceutical companies, clinical research organizations
Common Search & ComparisonYesYes

Global Biostatistics and Clinical Biostatistics share similar educational backgrounds and skills. However, Global Biostatistics focuses on international, multi-country health projects, while Clinical Biostatistics concentrates on clinical trials within specific sites or regions. Both roles are vital in the healthcare industry but differ mainly in scope and geographic focus.

How does a global biostatistician typically collaborate with international cross-functional teams?

Global Biostatistics professionals regularly work with diverse teams, including clinical researchers, data managers, regulatory affairs, and medical writers across multiple countries. They coordinate statistical analyses, ensure data integrity, and help interpret results in the context of global regulatory requirements. Effective communication and adaptability are essential, as teams may operate in different time zones and follow varied guidelines. Building strong cross-cultural relationships and understanding local regulatory nuances are key to successful collaboration in this role.
More about Global Biostatistics jobs
Infographic showing various Global Biostatistics job openings in the United States as of August 2026, with employment types broken down into 1% Internship, 83% Full Time, 11% Part Time, 4% Contract, and 1% Nights. Highlights an 88% Physical, 4% Hybrid, and 8% Remote job distribution, with an average salary of $119,702 per year, or $57.5 per hour.

Associate Director, Biostatistics

Sironax

Waltham, MA โ€ข On-site

Other

This job post hasย expired today.ย Applications are no longer accepted.


Job description

This role requires 3 days per week in Waltham, MA office


Position Overview

Sironax is seeking a highly motivated and experienced Associate Director, Biostatistics to play a critical role within our global clinical development organization. This position combines strategic statistical ownership with hands-on analytical expertise, offering a unique opportunity to influence clinical trial design, regulatory strategy, and corporate milestones.

The ideal candidate is adaptable, collaborative, and thrives in a fast-paced biotech environment. You will provide statistical support across clinical development programs while also supporting high-priority internal analyses, executive presentations, and regulatory reporting activities across multiple therapeutic areas, including rare diseases.


Key Responsibilities

  • Provide statistical ownership for the design, conduct, analysis, and reporting of clinical trials, including protocol development, statistical analysis plans (SAPs), and sample size and power calculations.
  • Serve as lead biostatistician on assigned clinical programs, partnering with cross-functional teams to align statistical strategy with overall development goals.
  • Lead oversight and management of CROs and external vendors to ensure timely, high-quality, and scientifically sound biostatistics deliverables.
  • Collaborate closely with cross-functional teams including Statistical Programming, Clinical Operations, Data Management, Regulatory Affairs, and Investor Relations.
  • Maintain alignment across global teams, including effective collaboration with US- and China-based stakeholders across multiple time zones.
  • Ensure compliance with CDISC standards, ICH guidelines, and FDA/EMA regulatory requirements.
  • Author and review statistical sections of protocols, SAPs, clinical study reports, and regulatory submission documents.
  • Provide statistical input for regulatory interactions, including briefing documents and responses to health authority queries.
  • Support biostatistics activities across a diverse clinical pipeline, including complex and data-limited rare disease programs.
  • Contribute to process improvement initiatives, statistical standards, and operational efficiencies within the biostatistics function.


Qualifications

  • Masterโ€™s or Ph.D. in Statistics, Biostatistics, or a related quantitative discipline.
  • Minimum of 8 years of biostatistics experience within the biotechnology or pharmaceutical industry.
  • At least 2 years of leadership, vendor oversight, or project management experience.
  • Advanced proficiency in SAS and/or R programming for statistical analysis; hands-on analytical capability strongly preferred.
  • Strong knowledge of CDISC standards (SDTM and ADaM), ICH guidelines, and regulatory submission requirements.
  • Experience supporting regulatory submissions and corporate milestones such as investor presentations or fundraising activities is preferred.
  • Excellent communication and collaboration skills with the ability to work effectively in a global environment.


What Weโ€™re Looking For

  • A proactive biostatistician who is comfortable balancing strategic oversight with hands-on execution.
  • An agile and adaptable professional who thrives in dynamic, fast-moving environments.
  • A collaborative team player with experience managing global stakeholders and cross-functional partnerships.
  • A solution-oriented thinker capable of navigating the unique challenges associated with rare disease clinical development.



About Sironax

Sironax is a global clinical-stage biotechnology company focused on developing innovative therapies for neurodegenerative, inflammatory, immunologic, and rare diseases. Driven by scientific excellence and a patient-centered mission, Sironax is expanding its global presence to transform treatment paradigms and improve outcomes for patients worldwide.


Equal Opportunity Employer

Sironax is an equal opportunity employer committed to diversity, equity, and inclusion. We welcome applicants from all backgrounds and are dedicated to creating a work environment where everyone feels valued and empowered.