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Associate Director Biostatistician Jobs (NOW HIRING)

Associate Director, Biostatistics Salary Range: $145K-$160K Location: Sommerset, NJ (Hybrid or Remote) About Pharmaron Pharmaron is a global contract research and manufacturing organization (CRO/CDMO ...

Responsibilities The Associate Director, Biostatistics has sufficient experience working as a statistician in the pharmaceutical industry to independently perform and lead statistical work within a ...

As an Associate Director, Biostatistician, you will be a champion of Otsuka's culture and values and will be responsible for providing statistical expertise/input in drug development including ...

Associate Director, Biostatistics

Somerset, NJ · On-site +1

$145K - $160K/yr

Associate Director, Biostatistics Salary Range: $145K-$160K Location: Sommerset, NJ (Hybrid or Remote) About Pharmaron Pharmaron is a global contract research and manufacturing organization (CRO/CDMO ...

... and experienced Associate Director, Biostatistics to play a critical role within our global ... Serve as lead biostatistician on assigned clinical programs, partnering with cross-functional teams ...

... and experienced Associate Director, Biostatistics to play a critical role within our global ... Serve as lead biostatistician on assigned clinical programs, partnering with cross-functional teams ...

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Associate Director Biostatistician information

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How much do associate director biostatistician jobs pay per hour?

As of Aug 13, 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.

More about Associate Director Biostatistician jobs
What cities are hiring for Associate Director Biostatistician jobs? Cities with the most Associate Director Biostatistician job openings:
What states have the most Associate Director Biostatistician jobs? States with the most job openings for Associate Director Biostatistician jobs include:
What job categories do people searching Associate Director Biostatistician jobs look for? The top searched job categories for Associate Director Biostatistician jobs are:
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 67% In-person, and 33% Remote job distribution, with an average salary of $119,702 per year, or $57.5 per hour.

Associate Director, Biostatistics

Otsuka Pharmaceutical Co., Ltd

Rockville, MD • On-site

$169.22 - $253/hr

Other

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 3 days ago


Job description

Associate Director, Biostatistician

Otsuka Pharmaceutical Company, a global healthcare company, seeks an Associate Director, Biostatistician to provide statistical leadership for early development programs including FIH, Phase1, Phase1b/2a, and proof-of-concept studies.

Responsibilities
  • Provide strategic statistical leadership for early development programs.
  • Lead statistical input into study design, protocol development, analysis planning, interpretation, and reporting of early-phase clinical trials.
  • Develop innovative statistical strategies to address key development questions related to safety, dose selection, proof‑of‑concept, and go/no‑go decisions.
  • Serve as the lead statistician for one or more assets and represent Biostatistics on cross‑functional asset teams.
  • Partner closely with Clinical Development, Clinical Pharmacology, Clinical Management, Regulatory Affairs, Data Management, and Statistical Programming.
  • Drive evidence‑based decision‑making through integration of safety, efficacy, PK/PD, biomarker, and translational data.
  • Support key development milestones, including proof‑of‑concept evaluations, dose selection, and development planning.
  • Influence program strategy by assessing development risks and recommending statistically sound approaches to maximize probability of success.
  • Serve as the Biometrics Trial Lead (BTL) and provide expertise and input regarding statistical analysis, TFLs format and data collection and quality, and overall timeline.
  • Manage, mentor, and develop biostatisticians, fostering technical excellence.
Qualifications / Required Experience
  • In‑depth knowledge of statistical principles, applications, and SAS/R programming software.
  • Strong computer skills with demonstrated experience in Microsoft Word, Excel, PowerPoint, and Outlook.
  • Demonstrated experience leading Phase1 and early‑phase clinical studies including FIH, dose escalation, dose expansion, and proof‑of‑concept trials.
  • Strong working knowledge of applicable U.S. regulatory requirements for clinical trial design, analysis, and reporting.
  • Proven ability to partner effectively with Clinical Development, Clinical Pharmacology, Translational Medicine, Regulatory Affairs, and other key stakeholders.
  • Experience working within matrixed, multidisciplinary drug development teams.
  • Ability to influence decisions in a matrix environment without direct authority.
  • Demonstrated ability to support and champion novel statistical approaches that improve decision‑making when working with limited or variable early‑phase clinical data.
  • Strong ability to communicate complex statistical concepts and insights clearly to technical and non‑technical audiences.
  • Education: PhD or Master’s degree in Statistics or Biostatistics with Minimum 7 years (PhD) or 9 years (Master’s) of experience in the pharmaceutical industry.
  • Experience in CNS area is a plus.
  • Experience with early phase clinical trials, preferably first‑in‑human or PK/PD/biomarker‑focused studies is a plus.
Benefits
  • Comprehensive medical, dental, vision, and prescription drug coverage.
  • Company‑provided Basic Life, AD&D, Short‑term and Long‑term Disability insurance.
  • Tuition reimbursement.
  • 401(k) match.
  • Paid holidays, paid leave programs, and other company‑provided benefits.
Competencies
  • Accountability for Results.
  • Strategic Thinking & Problem Solving.
  • Patient & Customer Centricity.
  • Impactful Communication.
  • Influence at all levels.
  • Respectful Collaboration.
  • Empowered Development.
Compensation

Minimum $169,222.00 – Maximum $253,000.00, plus incentive opportunity. The range shown represents a typical pay range for individuals hired in the U.S.

Equal Opportunity Employer

Otsuka is an equal opportunity employer. All qualified applicants are encouraged to apply and will be given consideration for employment without regard to race, color, sex, gender identity or gender expression, sexual orientation, age, disability, religion, national origin, veteran status, marital status, or any other legally protected characteristic.

Disclaimer

This job description is intended to describe the general nature and level of the work being performed by the people assigned to this position. It is not intended to include every job duty and responsibility specific to the position. Otsuka reserves the right to amend and change responsibilities to meet business and organizational needs as necessary.

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