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Manager Biostatistics Jobs (NOW HIRING)

Legend Biotech USA, Inc.

Collaborate closely with Biostatistics, Clinical Development, Clinical Operations, Data Management,Translational research and Medical teams to ensure alignment of analyses with protocol objectives ...

DBV Technologies

$185 - $215/hr

In close collaboration with Clinical, Medical, Regulatory, and Data Management, the role ensures ... Provide biostatistical leadership to support clinical development strategy, protocol design, and ...

Exelixis

Associate Biostatistics Director

Alameda, CA · On-site

$166K - $236K/yr

Works collaboratively with clinicians, data managers, biostatisticians, statistical programmers, and medical writers in the planning, conduct and analysis of clinical trials. Essential Duties And ...

Exelixis

Associate Biostatistics Director

Alameda, CA · On-site

$166K - $236K/yr

Works collaboratively with clinicians, data managers, biostatisticians, statistical programmers, and medical writers in the planning, conduct and analysis of clinical trials. Essential Duties And ...

Tempus

Director, Biostatistics

Boston, MA

$190K - $260K/yr

Demonstrated management skills; ability to manage the work of Ph.D./MS level biostatisticians, and have developed training for junior statisticians new to the industry. * Experience working with ...

Tempus

Director, Biostatistics

Chicago, IL · On-site

$190K - $260K/yr

Demonstrated management skills; ability to manage the work of Ph.D./MS level biostatisticians, and have developed training for junior statisticians new to the industry. * Experience working with ...

Tempus

Director, Biostatistics

Redwood City, CA

$190K - $260K/yr

Demonstrated management skills; ability to manage the work of Ph.D./MS level biostatisticians, and have developed training for junior statisticians new to the industry. * Experience working with ...

Tempus

Director, Biostatistics

Triangle, VA · On-site

$190K - $260K/yr

Demonstrated management skills; ability to manage the work of Ph.D./MS level biostatisticians, and have developed training for junior statisticians new to the industry. * Experience working with ...

Tempus

Director, Biostatistics

Chicago, IL · On-site

$190K - $260K/yr

Demonstrated management skills; ability to manage the work of Ph.D./MS level biostatisticians, and have developed training for junior statisticians new to the industry. * Experience working with ...

Verastem

Senior Director Biostatistics

Boston, MA · On-site

$250K - $300K/yr

Serve as a biostatistics leader within the organization, and manage statistical efforts for multiple clinical studies across a clinical program; provide leadership and guidance to other members of ...

Spyre Therapeutics

OR · On-site

$290K/yr

Lead the biometrics team including statistician, data manager, and statistical programmer at a ... Build and develop efficient biostatistical processes and standards, when appropriate Ideal ...

Servier

Director, Biostatistics

Boston, MA

Act as the biostatistics expert and leader, serve as primary statistical representative for cross ... cycle management * Ability to determine appropriate designs and analyses for clinical trials or ...

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How much do manager biostatistics jobs pay per year?

As of Jul 18, 2026, the average yearly pay for manager biostatistics in the United States is $137,055.00, according to ZipRecruiter salary data. Most workers in this role earn between $110,500.00 and $168,500.00 per year, depending on experience, location, and employer.

What are Manager Biostatistics?

A Manager Biostatistics is a professional who leads a team of biostatisticians in designing, analyzing, and interpreting data from clinical trials and research studies, primarily in the pharmaceutical, biotechnology, or healthcare industries. They oversee the statistical aspects of projects, ensure compliance with regulatory guidelines, and collaborate with cross-functional teams such as clinical, regulatory, and data management. Their responsibilities also include mentoring team members, managing project timelines, and contributing to the development of statistical analysis plans and reports.

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

To thrive as a Manager Biostatistics, you need advanced knowledge of statistical methodologies, clinical trial design, and a graduate degree in biostatistics or a related field. Proficiency with statistical software such as SAS, R, and experience with data management systems are typically required, alongside possible certifications like SAS Certified Specialist. Strong leadership, communication, and project management skills are essential for effectively guiding teams and collaborating with cross-functional stakeholders. These competencies ensure accurate data analysis, high-quality research, and successful project delivery in regulated environments.

How does a Manager of Biostatistics typically collaborate with clinical and regulatory teams during drug development projects?

As a Manager of Biostatistics, you play a pivotal role in cross-functional collaboration, especially with clinical and regulatory teams. You’ll work closely with clinical researchers to design studies, establish statistical analysis plans, and interpret results, ensuring the scientific rigor of the data. In addition, you’ll support regulatory submissions by preparing statistical reports and addressing queries from regulatory agencies. Effective communication and the ability to translate complex statistical concepts for non-statistical team members are essential for success in this role.
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Manager Biostatistics jobs near you
Infographic showing various Manager Biostatistics job openings in the United States as of July 2026, with employment types broken down into 1% Locum Tenens, 40% Full Time, 14% Part Time, 1% Contract, 41% Nights, and 3% Summer. Highlights an 65% Physical, 2% Hybrid, and 33% Remote job distribution, with an average salary of $137,055 per year, or $65.9 per hour.

Associate Director, Biostatistics

Summit Therapeutics

Palo Alto, CA

Other

Posted 17 days ago

Job description

Overview of Role:

Serves as the study-level biostatistician including reviewing protocol, conducting sample size calculations, developing statistical analysis plan, data presentation plan, and Data Monitoring Committee (DMC) charter, reviewing study documents (e.g., CRFs, ADaM specifications, statistical outputs, etc.) for clinical trials in oncology. Partners with cross-functional team members in ensuring accuracy/consistency of clinical data and exceptional delivery, interpretation of clinical results, and assists in the development and review of regulatory submission documents. Implements biostatistics department policies, standards, procedures, and work instructions.

Role and Responsibilities:

  • Provide statistical support to clinical development through the conduct of clinical studies in oncology
  • Conduct sample size calculations and develop statistical analysis plans (SAPs), data presentation plans, and DMC charters.
  • Collaborate with clinical operations, data management and CRO to develop and implement CRFs, database design, and the overall data quality plan
  • Review study documents (e.g., protocol, vendor data transfer specifications, ADaM specifications, statistical outputs) for clinical trials in oncology.
  • Review the accuracy of clinical data, perform statistical analysis, ensure the application of appropriate statistical methods, interpret study results, and collaborate with clinical team and other team members to produce interim reports, final clinical study reports
  • Contribute to the preparation of manuscripts for publication, ensuring accurate statistical reporting of research findings.
  • Develop and implement new statistical methodologies that enhance study design and analysis
  • Reviews and analyzes safety reporting, biomarker analyses and other aspects of clinical trial monitoring.
  • Independently defines required resources for assigned work, seeking advice as needed.
  • Work with department leader to develop and implement department policies, standards and procedures
  • Adheres to regulatory requirements of study conduct, statistical analysis principles, industry standards, and company SOPs.

Experience, Education and Specialized Knowledge and Skills:

  • Ph.D. in Statistics, Biostatistics or equivalent area with 6+ years biopharmaceutical industry experience required. MS degree in related discipline with extensive industry and leadership experience (8+ years) can be considered.
  • Strong proficiencies in software and other tools typically used by Biostatistics (e.g. SAS, R)
  • Good understanding of clinical trial processes and statistical programming requirements
  • Working knowledge of ICH, FDA and GCP regulations and guidelines
  • Attention to detail, accuracy and confidentiality
  • Clear and concise oral and written communication skills
  • Must be able to effectively multi-task and manage time-sensitive and highly confidential documents.
  • Communicate effectively and articulate complex ideas in an easily understandable way
  • Work in a fast-paced, demanding and collaborative environment

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