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Cro Biostatistician Jobs (NOW HIRING)

LanceSoft Inc

Biostatistician

Woodcliff Lake, NJ

Oversee CRO programming activities, perform quality assurance checks on internally or externally ... Must have a MS in Biostatistics/Statistics with at least 5 years of experience or a PhD in ...

EDETEK

Senior Biostatistician

The Senior Biostatistician provides statistical support and leadership for oncology clinical trials ... Candidates with CRO experience are strongly preferred. Experience supporting oncology studies and ...

micro1 AI

Biostatistician

Joliet, IL · Remote

$60 - $65/hr

Preferred Qualifications * 5+ years as a biostatistician supporting clinical trials at a sponsor, CRO, or academic trials unit. * Hands-on experience producing or quality controlling TFLs for ...

micro1 AI

Biostatistician

El Paso, TX · Remote

$60 - $65/hr

Preferred Qualifications * 5+ years as a biostatistician supporting clinical trials at a sponsor, CRO, or academic trials unit. * Hands-on experience producing or quality controlling TFLs for ...

micro1 AI

Biostatistician

High Point, NC · Remote

$60 - $65/hr

Preferred Qualifications * 5+ years as a biostatistician supporting clinical trials at a sponsor, CRO, or academic trials unit. * Hands-on experience producing or quality controlling TFLs for ...

micro1 AI

Biostatistician

Indianapolis, IN · Remote

$60 - $65/hr

Preferred Qualifications * 5+ years as a biostatistician supporting clinical trials at a sponsor, CRO, or academic trials unit. * Hands-on experience producing or quality controlling TFLs for ...

micro1 AI

Biostatistician

Raleigh, NC · Remote

$60 - $65/hr

Preferred Qualifications * 5+ years as a biostatistician supporting clinical trials at a sponsor, CRO, or academic trials unit. * Hands-on experience producing or quality controlling TFLs for ...

micro1 AI

Biostatistician

Irving, TX · Remote

$60 - $65/hr

Preferred Qualifications * 5+ years as a biostatistician supporting clinical trials at a sponsor, CRO, or academic trials unit. * Hands-on experience producing or quality controlling TFLs for ...

micro1 AI

Biostatistician

Gilbert, AZ · Remote

$60 - $65/hr

Preferred Qualifications * 5+ years as a biostatistician supporting clinical trials at a sponsor, CRO, or academic trials unit. * Hands-on experience producing or quality controlling TFLs for ...

micro1 AI

Biostatistician

Lubbock, TX · Remote

$60 - $65/hr

Preferred Qualifications * 5+ years as a biostatistician supporting clinical trials at a sponsor, CRO, or academic trials unit. * Hands-on experience producing or quality controlling TFLs for ...

micro1 AI

Biostatistician

Boise, ID · Remote

$60 - $65/hr

Preferred Qualifications * 5+ years as a biostatistician supporting clinical trials at a sponsor, CRO, or academic trials unit. * Hands-on experience producing or quality controlling TFLs for ...

micro1 AI

Biostatistician

Winston Salem, NC · Remote

$60 - $65/hr

Preferred Qualifications * 5+ years as a biostatistician supporting clinical trials at a sponsor, CRO, or academic trials unit. * Hands-on experience producing or quality controlling TFLs for ...

micro1 AI

Biostatistician

Philadelphia, PA · Remote

$60 - $65/hr

Preferred Qualifications * 5+ years as a biostatistician supporting clinical trials at a sponsor, CRO, or academic trials unit. * Hands-on experience producing or quality controlling TFLs for ...

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How much do cro biostatistician jobs pay per hour?

As of Aug 9, 2026, the average hourly pay for cro biostatistician 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 a CRO biostatistician?

CRO Biostatisticians are statistical experts who work at Contract Research Organizations (CROs) to design, analyze, and interpret data from clinical trials and other research studies for pharmaceutical, biotechnology, and medical device companies. They ensure that studies are statistically sound and compliant with regulatory requirements. Their work is essential for determining the safety and efficacy of new drugs or treatments, and they collaborate closely with clinical teams, data managers, and regulatory agencies. CRO Biostatisticians also play a key role in preparing statistical analysis plans and contributing to regulatory submissions.

What are some common challenges faced by CRO biostatisticians when collaborating with cross-functional teams during clinical trials?

CRO Biostatisticians often work closely with clinical, data management, and regulatory teams, which can present challenges such as aligning statistical analysis plans with evolving study protocols, managing large and complex datasets, and ensuring clear communication of statistical concepts to non-statistical colleagues. Effective collaboration is essential, as miscommunication can impact timelines or data quality. Developing strong interpersonal and project management skills can help Biostatisticians navigate these challenges and contribute to successful clinical trial outcomes.

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

To thrive as a CRO Biostatistician, you need a strong background in statistics, mathematics, and clinical research, typically supported by a master's or doctoral degree in biostatistics or a related field. Proficiency in statistical analysis software such as SAS, R, and understanding of CDISC standards are commonly required, along with knowledge of regulatory guidelines. Strong analytical thinking, attention to detail, and effective communication skills help in interpreting complex data and collaborating with multidisciplinary teams. These skills ensure the accuracy and integrity of clinical trial analyses, supporting regulatory submissions and successful drug development.
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Infographic showing various Cro Biostatistician job openings in the United States as of August 2026, with employment types broken down into 95% Full Time, 2% Part Time, and 3% Contract. Highlights an 70% Physical, 3% Hybrid, and 27% Remote job distribution, with an average salary of $119,702 per year, or $57.5 per hour.

Associate Director, Biostatistics (Late Stage)

Merck & Co.

Basking Ridge, NJ • On-site

$175.44 - $263.16/hr

Other

Posted 4 days ago

Merck rating

8.0

Company rating: 8.0 out of 10

Based on 51 frontline employees who took The Breakroom Quiz

43rd of 86 rated pharmaceutical

Job description

Job Summary

Position leads complex studies in study design, statistical analysis and interpretation of results with some supervision. This role contributes to specific aspects of drug development plans with minimal supervision and contributes to documents submitted to Health Authorities globally with some supervision. The position guides contract research organization (CRO) programmers and statisticians in preparing analysis files and performing statistical analyses, while interacting with study teams, as well as statisticians and programmers at CROs. The role works under some supervision to solve complex study problems.

Responsibilities
  • Leads statistical activities for complex studies including study design, protocol development, CRF review, SAP development, analysis file development, statistical analysis accuracy validation, results interpretation, and CSR input and review. Acts as main statistical contact for the assigned studies and projects.
  • Provides guidance to study team on all aspects of statistical activities; collaborates closely with data manager to ensure high quality data.
  • Provides input to multiple aspects of the development plan to ensure the study designs at each phase of the development are scientifically sound, can fulfill regulatory requirements and deliver the pre-specified product profile.
  • Reviews CRO/vendor proposals and budgets, establishes procedures through regular interaction, sets expectations on deliverables and timelines to guide CRO biostatistician and statistical programmers, and ensures deliverables are accurate and delivered according to the timelines.
  • Contributes to documents submitted to Health Authorities globally by providing input for the interaction or by writing the interaction document, and may participate in meetings or teleconferences with Health Authorities.
  • Primarily participates and may occasionally lead moderately complex initiatives, with some level of supervision, to improve the harmonization and efficiency of drug development, leading to cost savings and shortened timelines for the company.
Qualifications

Education Qualifications

  • Master's Degree in Statistics or Biostatistics required.
  • PhD in Statistics or Biostatistics preferred.

Experience Qualifications

  • 8+ Years of relevant experience in the pharmaceutical industry with a master’s degree required.
  • 5+ Years of relevant experience in the pharmaceutical industry with a PhD preferred.

Travel Requirements

  • Ability to travel up to 10% of the time.
Equal Opportunity Statement

Daiichi Sankyo, Inc. is an equal opportunity/affirmative action employer. Qualified applicants will receive consideration for employment without regard to sex, gender identity, sexual orientation, race, color, religion, national origin, disability, protected veteran status, age, or any other characteristic protected by law.

Salary Range

USD$175,440.00 - USD$263,160.00

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