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Associate Director Biostatistics Jobs (NOW HIRING)

Emmes

Associate Director Biostatistics

Rockville, MD · Remote

We believe the work we do will have a direct impact on patients' lives and act accordingly. We strive to build a collaborative culture at the intersection of being a performance and people driven ...

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 ...

Gilead

Director, Biostatistics

Foster City, CA · On-site

The Director will be primarily responsible for the business, operational, and compliance aspects of ... Works collaboratively with Statistical Programmers, Biostatisticians, Clinical Research Associates ...

Gilead

Director, Biostatistics

Parsippany, NJ · On-site

The Director will be primarily responsible for the business, operational, and compliance aspects of ... Works collaboratively with Statistical Programmers, Biostatisticians, Clinical Research Associates ...

Gilead

Director, Biostatistics

Parsippany, NJ

The Director will be primarily responsible for the business, operational, and compliance aspects of ... Works collaboratively with Statistical Programmers, Biostatisticians, Clinical Research Associates ...

Gilead

Director, Biostatistics

Foster City, CA

The Director will be primarily responsible for the business, operational, and compliance aspects of ... Works collaboratively with Statistical Programmers, Biostatisticians, Clinical Research Associates ...

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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Associate Director Biostatistics information

See salary details

$30.5K

$102.7K

$173K

How much do associate director biostatistics jobs pay per year?

As of Jul 15, 2026, the average yearly pay for associate director biostatistics in the United States is $102,728.00, according to ZipRecruiter salary data. Most workers in this role earn between $70,000.00 and $141,000.00 per year, depending on experience, location, and employer.

What are some common challenges an Associate Director of Biostatistics faces when leading cross-functional project teams?

As an Associate Director of Biostatistics, one common challenge is balancing statistical rigor with project timelines, especially when collaborating with clinical, regulatory, and data management teams. You often need to translate complex statistical concepts for non-statistical colleagues while ensuring data integrity and compliance with regulatory standards. Managing multiple projects simultaneously and mentoring junior statisticians also requires strong organizational and leadership skills. Effective communication and adaptability are key to navigating the dynamic environment typical in pharmaceutical and biotech organizations.

What does an Associate Director of Biostatistics do?

An Associate Director of Biostatistics is responsible for leading biostatistical support for clinical trials and research studies, often within pharmaceutical, biotechnology, or medical research organizations. They manage teams of biostatisticians, oversee statistical analysis plans, ensure compliance with regulatory requirements, and collaborate with cross-functional teams. Their role also involves reviewing and interpreting data, contributing to study design, and providing strategic input for data-driven decision-making. This position typically requires advanced knowledge of statistical methods and experience in clinical research.

What is the difference between Associate Director Biostatistics vs Senior Biostatistician?

AspectAssociate Director BiostatisticsSenior Biostatistician
CredentialsMaster's or PhD in Biostatistics or related fieldMaster's or PhD in Biostatistics or related field
Work EnvironmentLeadership role in clinical trials, overseeing teamsHands-on statistical analysis, supporting projects
Employer & Industry UsagePharmaceuticals, biotech companies, CROsPharmaceuticals, biotech, research institutions

The main difference between Associate Director Biostatistics and Senior Biostatistician lies in their responsibilities and seniority. The Associate Director typically has leadership duties, overseeing teams and strategic planning, while the Senior Biostatistician focuses on conducting complex analyses and supporting project execution. Both roles require similar educational backgrounds and are common in the pharmaceutical and biotech industries.

What are the key skills and qualifications needed to thrive as an Associate Director Biostatistics, and why are they important?

To thrive as an Associate Director Biostatistics, you need advanced expertise in statistical methodologies, clinical trial design, and a graduate degree (often PhD or MS) in biostatistics or a related field. Proficiency with statistical software such as SAS, R, and experience with regulatory submission requirements are typically necessary, along with knowledge of CDISC standards. Strong leadership, communication, and project management skills enable effective collaboration with cross-functional teams and mentoring of junior statisticians. These competencies are vital to ensure rigorous data analysis, regulatory compliance, and the successful delivery of clinical research projects.
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Associate Director Biostatistics jobs near you
Infographic showing various Associate Director Biostatistics job openings in the United States as of July 2026, with employment types broken down into 100% Full Time. Highlights an 61% In-person, 8% Hybrid, and 31% Remote job distribution, with an average salary of $102,728 per year, or $49.4 per hour.
Associate Director, Biostatistics - Remote

Associate Director, Biostatistics - Remote

Penfield Search Partners

Fairfield, CT • On-site, Remote

Full-time

Posted 28 days ago

Job description

Contact: Neisha Camacho/Terra Parsons -
No 3rd party candidates
Job Overview

We are seeking a highly skilled and motivated Biostatistician to lead our biometrics function across multiple studies in one of the late-phase programs for cardiovascular drug development. As the AD Biostatistician, you will be the study lead, representing biometrics in cross functional team meetings. You will be responsible for discussing and shaping the clinical development plan, study design, endpoint selection, statistical analysis plan, and regulatory submission and publication strategy to support pursuant of precision medicine. This role involves overseeing CROs and collaborating with cross-functional teams to deliver high-quality analysis outputs and interpret results.

Essential Duties And Responsibilities

  • Collaborate with clinical, regulatory, medical affairs, and other teams to ensure cohesive and integrated project strategies.
  • Contribute to clinical protocol development and study reports, including authoring of the Statistics section and reviewing of other sections by applying statistical principles.
  • Author or review statistical analysis plans for clinical trials and for integrated summaries of safety/effectiveness (ISS/ISE), and author or oversee the development of shells for tables, figures and listings.
  • Review case report form (CRF) designs to ensure data collection meet the requirements of statistical analyses.
  • Provide statistical input to data monitoring committee (DMC) charters.
  • Oversee the CROs or internal teams to deliver high-quality and timely analysis outputs and interpret the results.
  • Manage statistical activities in support of NDA/MAA or other regulatory submissions.
  • Address statistical questions/comments from FDA and other regulatory agencies.
  • Support and contribute to the preparation of publications, including manuscripts, posters and oral presentations.
  • Contribute or lead standardization and process improvement efforts for Biostatistics and contributes to cross-functional process improvement efforts.
  • Provide guidance and oversight to ensure compliance with regulatory standards and best practices.
  • Mentor junior statisticians.

Qualifications And Preferred Skills

  • PhD in Statistics, Biostatistics, or a related scientific field with 7+ years of experience, or MS with 10+ years of experience in clinical trials, drug development, the pharmaceutical industry, or healthcare.
  • Expertise in applying knowledge of general and cutting edge statistical / clinical trials methodology to solve complex statistical problems in the clinical development area and ensure alignment with regulatory agencies and industry standards.
  • Knowledgeable of machine learning approaches for classification and predictive modeling.
  • Excellent communication and presentation skills, with the ability to convey complex statistical concepts to non-statisticians.
  • Strong knowledge and hands-on experience of statistical software (SAS, R or Python) and proficiency in implementation of advanced analytical methods especially for data visualization.
  • Experience in managing CROs and collaborating with cross-functional teams.
  • Experience with NDAs, and MAA’s is highly desired.
  • Experience with cardiovascular drug development and digital health data or real-world data is preferred.
  • Demonstrated ability to work independently and as part of a team in a fast-paced, dynamic environment.