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Associate Biostatistician Jobs (NOW HIRING)

Amgen

Biostatistics Sr Mgr

Washington, DC

Biostatistics Senior Manager What you will do Let's do this. Let's change the world. In this vital ... Associate's degree and 10 years of experience ORHigh school diploma / GED and 12 years of ...

Amgen, Inc.

Biostatistics Sr Mgr

Biostatistics Senior Manager What you will do Let's do this. Let's change the world. In this vital ... Associate's degree and 10 years of experience OR High school diploma / GED and 12 years of ...

Amgen

OR

Biostatistics Senior Manager What you will do Let's do this. Let's change the world. In this vital ... Associate's degree and 10 years ofexperience OR High school diploma / GED and 12 years of ...

Amgen

Biostatistics Senior Manager What you will do Let's do this. Let's change the world. In this vital ... Associate's degree and 10 years of experience OR High school diploma / GED and 12 years of ...

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How much do associate biostatistician jobs pay per hour?

As of May 28, 2026, the average hourly pay for associate 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 are the key skills and qualifications needed to thrive as an Associate Biostatistician, and why are they important?

To thrive as an Associate Biostatistician, you need a solid background in statistics, mathematics, and data analysis, typically supported by a degree in biostatistics, statistics, or a related field. Familiarity with statistical software such as SAS, R, or SPSS, along with knowledge of clinical trial processes, is commonly required. Strong analytical thinking, attention to detail, and effective communication skills help you interpret data accurately and collaborate with cross-functional teams. These skills are crucial for ensuring reliable data analysis and supporting sound scientific and regulatory decisions in research and healthcare.

What are typical projects or tasks an Associate Biostatistician works on within a clinical research team?

As an Associate Biostatistician, you can expect to work closely with clinical researchers to design studies, develop statistical analysis plans, and perform data analyses for clinical trials. Typical tasks include cleaning and validating datasets, generating tables and figures for reports, and assisting in the interpretation of statistical results. You may also collaborate with data managers, programmers, and senior statisticians to ensure data integrity and regulatory compliance. This role offers a dynamic environment where attention to detail and teamwork are essential.

What is an Associate Biostatistician?

An Associate Biostatistician is an entry-level professional who applies statistical methods to analyze data from biological, medical, or health-related research studies. They assist in designing experiments, managing data, and interpreting results to support scientific conclusions. Typically, they work under the supervision of senior biostatisticians or researchers in industries such as pharmaceuticals, healthcare, or academia. Their role is crucial in ensuring the validity and reliability of research findings.

What is the difference between Associate Biostatistician vs Biostatistician?

AspectAssociate BiostatisticianBiostatistician
Required CredentialsBachelor's or Master's in Biostatistics or related fieldMaster's or Ph.D. in Biostatistics or related field
Work EnvironmentEntry-level, supporting clinical trials and data analysisMore independent roles, leading projects and analyses
Employer & Industry UsagePharmaceutical companies, research institutions, biotech firmsSame as Associate Biostatistician, often with more senior responsibilities

The main difference between an Associate Biostatistician and a Biostatistician lies in experience and responsibility level. Associate Biostatisticians typically have less experience and focus on supporting data analysis tasks, while Biostatisticians often lead projects and make independent statistical decisions. Both roles are common in the pharmaceutical and research industries, with the Biostatistician role generally requiring more advanced education and experience.

More about Associate Biostatistician jobs
What cities are hiring for Associate Biostatistician jobs? Cities with the most Associate Biostatistician job openings:
What are the most commonly searched types of Biostatistician jobs? The most popular types of Biostatistician jobs are:
What states have the most Associate Biostatistician jobs? States with the most job openings for Associate Biostatistician jobs include:
What job categories do people searching Associate Biostatistician jobs look for? The top searched job categories for Associate Biostatistician jobs are:
Associate Biostatistician jobs near you
Infographic showing various Associate Biostatistician job openings in the United States as of May 2026, with employment types broken down into 2% Locum Tenens, 3% Internship, 36% As Needed, 40% Temporary, 18% Nights, and 1% Summer. Highlights an 97% Physical, 1% Hybrid, and 2% Remote job distribution, with an average salary of $119,702 per year, or $57.5 per hour.

Associate Director, Biostatistics

Kardigan

South San Francisco, CA • On-site

Other

Posted 17 days ago

Job description

Position Title: Associate Director (AD), Biostatistics

Department: Development - Data Science

Reports To: Director, Biostatistics

Location: South San Francisco, CA or Princeton, NJ - On-site 4 days per week (Mon to Thurs) 

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.

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