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Associate Director Biostatistician Jobs (NOW HIRING)

Gilead

Assoc Director, Biostatistics

Parsippany, NJ · On-site

$195K - $253K/yr

As an Associate Director, Biostatistics , at Gilead you will ... Key Responsibilities: * Works collaboratively with Statistical Programmers, Biostatisticians, Clinical Research Associates, Clinical ...

Gilead

Assoc Director, Biostatistics

Parsippany, NJ

$195K - $253K/yr

As an Associate Director, Biostatistics , at Gilead you will ... Key Responsibilities: * Works collaboratively with Statistical Programmers, Biostatisticians, Clinical Research Associates, Clinical ...

BeiGene, Inc.

Associate Director, Biostatistics

$162K - $212K/yr

BeOne continues to grow at a rapid pace with challenging and exciting opportunities for experienced professionals. When considering candidates, we look for scientific and business professionals who ...

Vrtx

Biostatistics Associate Director (HYBRID)

Boston, MA · Hybrid

$174K - $262K/yr

Biostatistics Associate Director will perform sophisticated scientific statistical analyses in support of the company's Global Medicines Development and Affairs area with minimal guidance and ...

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How much do associate director biostatistician jobs pay per hour?

As of Aug 7, 2026, the average hourly pay for associate director 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 the difference between Associate Director Biostatistician vs Senior Biostatistician?

AspectAssociate Director BiostatisticianSenior Biostatistician
CredentialsTypically requires a Master’s or PhD in Biostatistics or related fieldSame as Associate Director, often with extensive experience
Work EnvironmentLeads projects, collaborates with cross-functional teams, involved in strategic planningExecutes statistical analyses, supports project teams, and mentors junior staff
Employer & Industry UsageUsed in pharmaceutical, biotech, and clinical research companies, often in leadership rolesCommon in similar industries, focusing on analysis and data interpretation

The main difference is that the Associate Director Biostatistician typically holds a leadership role with strategic responsibilities, while the Senior Biostatistician focuses more on technical analysis and project support. Both roles require advanced biostatistics expertise and similar educational backgrounds, but the Associate Director often oversees teams and manages project direction.

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Associate Director Biostatistician jobs near you
Infographic showing various Associate Director Biostatistician job openings in the United States as of August 2026, with employment types broken down into 100% Full Time. Highlights an 60% In-person, and 40% Remote job distribution, with an average salary of $119,702 per year, or $57.5 per hour.

Associate Director, Biostatistics

Summit Therapeutics

Palo Alto, CA • On-site

Full-time

Re-posted 14 hours ago

Job description

About Summit:
Summit Therapeutics Inc. is a biopharmaceutical oncology company with a mission focused on improving quality of life, increasing potential duration of life, and resolving serious unmet medical needs. At Summit, we believe in building a team of world class professionals who are passionate about this mission, and it is our people who drive this mission to reality. Summit's core values include integrity, passion for excellence, purposeful urgency, collaboration, and our commitment to people. Our employees are truly the heart and soul of our culture, and they are invaluable in shaping our journey toward excellence.
Summit's team is inspired to touch and help change lives through Summit's clinical studies in the field of oncology. Summit has multiple global Phase 3 clinical studies, including:
Non-small Cell Lung Cancer (NSCLC)
  • HARMONi: Phase 3 clinical study which was intended to evaluate ivonescimab combined with chemotherapy compared to placebo plus chemotherapy in patients with EGFR-mutated, locally advanced or metastatic non-squamous NSCLC who were previously treated with a 3rd generation EGFR TKI.
  • HARMONi-3: Phase 3 clinical study which is intended to evaluate ivonescimab combined with chemotherapy compared to pembrolizumab combined with chemotherapy in patients with first-line metastatic NSCLC.
  • HARMONi-7: Phase 3 clinical study which is intended to evaluate ivonescimab monotherapy compared to pembrolizumab monotherapy in patients with first-line metastatic NSCLC.

Colorectal Cancer (CRC)
  • HARMONi-GI3: Phase 3 clinical study intended to evaluate ivonescimab in combination with chemotherapy compared with bevacizumab plus chemotherapy.

Ivonescimab is an investigational therapy not presently approved by any regulatory authority other than China's National Medical Products Administration (NMPA). Summit is headquartered in Miami, Florida, and has additional offices in California, New Jersey, the UK, and Ireland.
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

This is the pay for this position
Pay Transparency
$190,000-$210,000 USD
Actual compensation packages are based on several factors that are unique to each candidate, including but not limited to skill set, depth of experience, certifications, and specific work location. This may be different in other locations due to differences in the cost of labor. The total compensation package for this position may also include bonus, stock, benefits and/or other applicable variable compensation.
Summit does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact Summit's Talent Acquisition team at recruiting@smmttx.com to obtain prior written authorization before referring any candidates to Summit.
Summit Therapeutics Inc. is an Equal Opportunity Employer and takes pride in creating and maintaining diverse environment. We do not discriminate in recruitment, hiring, training or promotion or any other employment practices for reasons of race, color, religion, gender, national origin, age, sexual orientation, marital or veteran status, disability, or any other legally protected status.

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