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Global Biostatistics Jobs (NOW HIRING)

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 ...

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 ...

$240 - $285/hr

Reporting to the Vice President, Biostatistics and Data Management, the Director/Senior Director ... Experience with solid tumor oncology and global NDA/BLA submissions preferred. * Experience with ...

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

Sr. Director, Biostatistics

Cambridge, MA ยท On-site

$270K - $290K/yr

Key contributor on regulatory submissions and communication with global regulatory authorities ... Oversee and lead the vendor/CRO biostatistics and programming teams, including activities during ...

Sr. Director, Biostatistics

Cambridge, MA ยท On-site

$270K - $290K/yr

Key contributor on regulatory submissions and communication with global regulatory authorities ... Oversee and lead the vendor/CRO biostatistics and programming teams, including activities during ...

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Global Biostatistics information

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How much do global biostatistics jobs pay per hour?

As of Sep 4, 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.

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.

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.

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 84% Full Time, 11% Part Time, 4% Contract, and 1% Nights. Highlights an 87% Physical, 4% Hybrid, and 9% Remote job distribution, with an average salary of $119,702 per year, or $57.5 per hour.

Sr. Director, Biostatistics

ALX Oncology Inc.

South San Francisco, CA โ€ข On-site

Full-time

Retirement

Re-posted 15 days ago


Job description

The Senior Director, Biostatistics provides strategic statistical leadership across ALX Oncology's clinical development portfolio, partnering cross-functionally to design, execute, analyze, and interpret clinical studies that support regulatory submissions and advance innovative oncology therapies. This role drives statistical strategy, oversees outsourced biostatistics activities, and collaborates closely with Clinical Development, Translational Medicine, Biomarker Sciences, Regulatory Affairs, Data Management, Statistical Programming, Clinical Operations, and external partners.

Preference will be given to candidates who can regularly work onsite Mondays and Tuesdays as part of the company's hybrid work model.

Key Responsibilities include:

  • Lead the Biostatistics function by developing and executing strategies that support ALX Oncology's clinical development portfolio, providing strategic leadership across oncology programs from early development through registration and lifecycle management.
  • Direct statistical strategy for registrational clinical trials, including innovative adaptive and biomarker-driven study designs, and provide expertise in study design, endpoint selection, estimands, multiplicity control, interim analyses, missing data, sensitivity analyses, and benefit-risk assessments.
  • Oversee the development, review, and approval of key statistical deliverables, including protocols, statistical analysis plans (SAPs), clinical study reports (CSRs), regulatory briefing documents, publications, and scientific presentations.
  • Drive adaptive design evaluations and statistical simulations to support study design, operating characteristics, power calculations, and informed decision-making throughout clinical development.
  • Provide statistical leadership for global regulatory interactions, health authority submissions, companion diagnostic (CDx) and biomarker-driven development programs, partnering closely with cross-functional teams to ensure compliance with applicable regulatory requirements and industry standards.
  • Oversee CROs, external statistical vendors, budgets, and outsourced Biostatistics activities, ensuring high-quality deliverables, effective governance, and operational excellence.
  • Provide technical leadership and mentorship across the Biometrics organization, fostering collaboration, innovation, and the adoption of statistical best practices.
  • Contribute to business development, due diligence, portfolio strategy, and other strategic initiatives as needed.
  • Contribute to a culture that reflects ALX's values by acting with integrity, accountability, transparency, and respect. Build strong, collaborative relationships through active engagement with colleagues, including regular onsite participation consistent with the company's hybrid work model.

Not sure if you are qualified for this position?ย  We know that skills and experience can show up in different ways and we welcome resumes from a broad range of applicants.ย  You are encouraged to apply even if you do not meet each of the preferred qualifications.

Preferred Qualifications include:

  • Bachelor's degree in Statistics, Biostatistics, Mathematics, Life Sciences, Computer Science, or a related quantitative discipline, or an equivalent combination of education and directly relevant work experience. Advanced degree (MS, PhD, or equivalent) in a quantitative discipline is strongly preferred.
  • Approximately 12+ years of progressive Biostatistics experience within biotechnology, pharmaceutical, or CRO environments, including Phase I-III oncology clinical studies, with demonstrated success leading statistical strategy for registrational clinical trials, partnering across cross-functional teams, and supporting global regulatory submissions.
  • Experience with companion diagnostic (CDx) co-development, biomarker-driven development strategies, and interactions with global health authorities.
  • Deep expertise in biostatistical principles, oncology clinical trial methodology, GCP, applicable regulatory requirements, and industry best practices including study design, adaptive clinical trial methodologies, survival analysis, estimands, multiplicity adjustment, missing data methodology, interim analyses, and companion diagnostic statistical approaches.
  • Proficiency with statistical programming and analysis software, including SAS and R. Experience with adaptive design and simulation software (e.g., EAST, ADDPLAN, or equivalent).
  • Strategic, collaborative leader with excellent communication, organizational, and relationship-building skills, capable of influencing cross-functional teams and external partners.
  • Demonstrated ability to prioritize competing demands, solve complex problems, build scalable processes, and adapt to evolving business priorities while contributing beyond functional boundaries in a fast-paced, resource-constrained environment.

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Compensation

The salary range for this position at our South San Francisco, CA corporate office is $240,000 - $280,000. Additional factors such as academic credentials and relevant experience will influence the actual salary offered. In addition to a competitive market-based salary, ALX Oncology offers the opportunity to participate in stock programs, a performance-based bonus, and a comprehensive benefits package including 401K. Additional information can be found here:ย  https://alxoncology.com/careers/

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About ALX Oncology

ALX Oncology (Nasdaq: ALXO) is a clinical-stage biotechnology company advancing a pipeline of novel therapies designed to treat cancer and extend patients' lives. ALX Oncology's lead therapeutic candidate, evorpacept, has demonstrated potential to serve as a cornerstone therapy upon which the future of immuno-oncology can be built. Evorpacept is currently being evaluated across multiple ongoing clinical trials in a wide range of cancer indications. ALX Oncology's second pipeline candidate, ALX2004, is a novel EGFR-targeted antibody-drug conjugate with a differentiated mechanism of action. A Phase 1, dose-escalation trial of ALX2004 is ongoing in patients with EGFR-expressing solid tumors. More information is available atย www.alxoncology.comย and on LinkedIn @ALX Oncology.

Information for Recruitment Agencies

Please note that ALX Oncology does not accept unsolicited resumes or candidate information from recruitment agencies, including blinded or anonymized resumes, and will not be responsible for any fees associated with unsolicited submissions.ย  Do not contact hiring managers or other ALX Oncology employees directly.ย Recruiting activities are managed through our Human Resources team.