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Manager Biostatistics Jobs (NOW HIRING)

Otsuka

Associate Director, Biostatistics

Princeton, NJ · On-site +1

Takes full responsibility in managing biostatistical tasks (as listed above) for one therapeutic area and provides strategic technical support to other clinical projects. * Provides technical ...

BeOne Medicines

Senior Statistician (RWD/RWE)

Manhattan, NY · On-site

$155K - $200K/yr

Other Qualifications Senior Manager, Biostatistics: PhD or equivalent degree in statistics/biostatistics or related discipline with a minimum of 2 years relevant work experience, or a Master's degree ...

Exelixis

Sr Biostatistics Director

Alameda, CA · On-site

Provides leadership within biostatistics function to develop and execute statistical strategy ... Manages timelines, deliverables and budgets of contract research organizations. Essential Duties ...

Exelixis

Associate Biostatistics Director

Alameda, CA · On-site

$166.50K - $236.50K/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

$166.50K - $236.50K/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

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

New York, NY

$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 ...

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 ...

Tempus

Director, Biostatistics

Triangle, VA

$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

$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 ...

Exelixis

Associate Biostatistics Director

Alameda, CA

$166.50K - $236.50K/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 ...

Spyre Therapeutics

OR

$275K - $290K/yr

The Sr. Director of Biostatistics will provide leadership and strategic input for clinical ... Lead the biometrics team including statistician, data manager, and statistical programmer at a ...

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Manager Biostatistics information

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$29.5K

$137.1K

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How much do manager biostatistics jobs pay per year?

As of May 28, 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 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.

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.
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Manager Biostatistics jobs near you
Associate Director, Biostatistics

Associate Director, Biostatistics

Zenas BioPharma

Waltham, MA • On-site

Full-time

Posted 28 days ago

Job description

Zenas is a clinical-stage global biopharmaceutical company committed to becoming a leader in the development and commercialization of transformative therapies for patients with autoimmune diseases. Our core business strategy combines our experienced leadership team with a disciplined product candidate acquisition approach to identify, acquire and develop product candidates globally that we believe can provide superior clinical benefits to patients living with autoimmune diseases. Zenas is advancing two late-stage, potential franchise molecules, obexelimab and orelabrutinib. Obexelimab, Zenas' lead product candidate, is a bifunctional monoclonal antibody designed to bind both CD19 and FcγRIIb, which are broadly present across B cell lineage, to inhibit the activity of cells that are implicated in many autoimmune diseases without depleting them. We believe that obexelimab's unique mechanism of action and self-administered, subcutaneous injection regimen may broadly and effectively address the pathogenic role of B cell lineage in chronic autoimmune disease. Orelabrutinib is a potentially best-in-class, highly selective CNS-penetrant, oral, small molecule Bruton's Tyrosine Kinase (BTK) inhibitor with the potential to address compartmentalized inflammation and disease progression in Multiple Sclerosis (MS). Zenas' earlier stage programs include ZB021, a clinical-stage, potentially best-in-class, oral, IL-17AA/AF inhibitor; ZB022, a preclinical, potentially best-in-class, oral, brain-penetrant, TYK2 inhibitor; and ZB014, a preclinical half-life extended anti-CD-19 and FcγRIIb monoclonal antibody.
We are seeking top talent who share our commitment to patients and have a track record of success in acquiring, developing and commercializing products across the globe. Our colleagues have an opportunity to engage in a fast-paced learning environment and experience individual and organizational success as we work towards becoming a global immunology and autoimmune disease leader, while living our values of Transparency, Relationships, Urgency, Excellence and Innovation - TRUE Innovation!
Position Summary:
The Associate Director, Biostatistics is responsible for leading the development and execution of statistical aspects for global clinical programs. He/she will provide project leadership and hands-on technical statistical support. This position reports to the Senior Director, Biostatistics.
Key Responsibilities:
  • Independently lead the development and execution of all statistical aspects for one or more clinical development programs, including contribution to study trial design, analysis planning, study results presentation and interpretation, clinical study report authoring, regulatory submissions, and publications.
  • Review or author statistical analysis sections of protocols, statistical analysis plans (SAP), clinical study reports (CSR), regulatory documents or scientific publications.
  • Generates or reviews study randomization, sample size/power estimations and key specifications for statistical programming implementation of analyses including programming specifications for analysis datasets and TLFs, including SDTM and ADaM specifications.
  • Manage biostatistics and programming vendors.
  • Develop statistical programs to ensure quality and accuracy or to perform other pre-specified or ad-hoc analyses as required.
  • Work as part of a collaborative, cross-functional team with members from other disciplines.
  • Represent Biostatistics, ensuring statistical input is provided throughout the clinical development process.
  • Interact with regulatory agencies, and effectively address statistical questions and requests.
  • Take accountability for ensuring quality in all planning, design, and execution of assignments associated with the assigned protocol or project.

Qualifications:
  • PhD or MSc in Biostatistics or related discipline, 8+ years' experience working across all phases of clinical trials in CRO/Biotech/ Pharmaceutical company.
  • Solid knowledge of statistical methodology, clinical experimental design and analysis for clinical trials.
  • Experience working with CROs and vendors.
  • Good knowledge of ICH, FDA, EMA, and NMPA guidelines.
  • Prior experience supporting global clinical trials.
  • Project leadership experience.
  • Submission experience is strongly preferred.
  • Exceptional interpersonal skills and problem-solving capabilities.
  • Excellent oral and written communication skills and ability to effectively communicate statistical concepts to both technical and non-technical stakeholders.
  • Experience working with cross-functional teams, including clinical development, regulatory affairs, medical affairs and commercial.
  • Experience working with CDISC data standards.
  • Proficiency in SAS programming and other statistical software tools.
  • Comfortable working in a demanding, fast-paced, start-up culture with evolving processes. Flexible and able to adapt to new situations as the business demands.
  • Demonstrates flexibility to work non-traditional work hours when needed, given international operations across time zones.

#LI-Hybrid
Zenas is committed to fair and equitable compensation practices. The base salary pay range for this role is $172,300 to 215,400. Actual compensation packages will depend on various factors, including, but not limited to depth of experience, education, skillset, overall performance and/or location.
Zenas believes in providing a competitive compensation and benefits package to all employees. Our base salary is just one component of Zenas' competitive total rewards strategy that also includes annual performance bonus, equity, full range of benefits and other incentive compensation plans.
Zenas BioPharma is proud to be an equal opportunity employer. We are committed to fostering an environment where diversity is valued. All qualified applicants will receive consideration for employment based on merit, qualifications and the needs of the business.

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