Biostatistician Jobs in the United States
Canfield Scientific, Inc
Parsippany, NJ
Canfield Scientific, Inc. is a core imaging lab providing custom photographic systems, image monitoring, and centralized analysis services for the pharmaceutical, biotechnology and cosmetics industries supporting global clinical trials providing primary endpoint data and supporting documentation. Contribute to the development and authoring of Statistical Analysis Plans (SAPs), including drafting key sections (analysis populations, endpoints, missing data handling, sensitivity analyses) under senior statistical guidance.
Daiichi Sankyo, Inc.
Bernards, NJ
Protocol Development, Case Report Form (CRF; review), Statistical Analysis Plan (SAP), Statistical Analysis, Results Interpretation, and clinical study report (CSR): Leads statistical activities for complex studies including study design, protocol development, CRF review, SAP development, analysis files development, statistical analysis accuracy validation, results interpretation and CSR input and review. May participate in meeting or teleconferences with Health Authorities Global BDO Strategy to Improve Drug Development: Primarily participates and may occasionally lead moderately complex initiatives, with some level of supervision, to improve the harmonization and efficiency of drug development which leads to cost savings and shortened timelines for the company.
Axio Research LLC
$88800 - $133200
Seattle, WA
Minimum Requirements: Master's degree in Biostatistics, Statistics, or a closely related field and 3 years of experience in biostatistics, including 2 years of experience with each of the following: Statistical experience in the drug development environment; experience conducting unblinded reviews in DMC activities, including charter, statistical analysis plan, mock shells, specifications, analysis, programming, and validation; and experience in reviewing and performing oversight of analysis plans, statistical analyses, outputs, and datasets for unblinded clinical trials. Axio Research, LLC (Seattle, WA) is seeking a Biostatistician to support teams of biostatisticians and statistical programmers in creating unblinded reports of confidential, ongoing clinical trial data for Data Monitoring Committees.
New York Medical College
Valhalla, New York
Overview: The biostatistician will support clinical epidemiology and biomedical research for the Campus Collaborative Research Core (CCRC) program and the Biostatistics Core at New York Medical College for both the college and Touro University. The biostatistician will design studies, collect, and analyze data from medical experiments, interpret the results of the analyses, and collaborate in writing articles to disseminate research findings.
Edwards Lifesciences
$132000 - $186000
Irvine, CA
The Principal Biostatistician will represent the Biostatistics department on all aspects of the clinical development process, ranging from clinical trial designs to regulatory submissions while applying scientific rigor to statistical methods and interpretation of results and also advise on the conduct of clinical studies, database development and data quality assurance with the analysis of clinical endpoints in mind. + Collaborate with core stakeholders to provide statistical expertise in support of new product development (NPD) and/or regulatory submissions (e.g., PMA, CE Mark, PMDA) and other regulatory documents as needed.
Arrowhead Pharmaceuticals
$130000 - $145000
Los Angeles, CA
As an internal expert in biostatistics, you will provide technical leadership and biostatistical input to closely collaborate with other functional teams at Arrowhead, including Clinical Development and Operations, Regulatory, Commercial, Program Management and others. Arrowhead is leading the field in bringing the promise of RNAi to address diseases outside of the liver, and our clinical pipeline includes disease targets in the liver and lung with a promising pipeline of preclinical candidates.
Emory University
Atlanta, Georgia
Works effectively within a group setting in areas of design of data collection instruments, study design, database management, statistical programming, analysis of data, statistical graphics, and writing of reports which include explanations of methods used and interpretation of results obtained. This position will be supported by a rich collection of population claims (SEER-Medicare, MarketScan), EHR data (EPIC COSMOS), and strong data and research infrastructure provided by the Department of Radiation Oncology, Division of Health Services, Policy, and Outcomes.
Parexel
Olympia, WA
Location** : United States - Remote **Key Accountabilities** : **Operational Execution** + Provide broad statistical support, including trial design, protocol and CRF development on specific studies + Lead production and quality control of randomization, analysis plans, statistical reports, statistical sections of integrated clinical reports and other process supporting documents + Perform sample-size calculations, generate randomization lists and write statistical methodology sections for inclusion in study protocols + Provide statistical input into Data Monitoring Committee (DMC) activities, including development of DMC charters and analysis plans + Provide a supporting role as a non-voting independent statistician providing data and analysis for DMC review **Business Development** + Support of Business Development, by actively contributing to study design considerations in internal and client meetings, providing and discussing sample size scenarios, support of budget and proposal development, attending and preparing bid defense meetings **General Activities** + Understand regulatory requirements related to the specific therapeutic areas and the implications for statistical processing and analysis + Understand, apply and provide training in extremely advanced and sometimes novel statistical methods + Contribute to the development and delivery of internal and external statistical training seminars and courses + Review position papers based on current good statistical practice + Interact with clients and regulatory authorities + Review publications and clinical study reports + Travel to, attend, and actively contribute to all kind of client meetings as appropriate (e.g. The Principal Biostatistician works independently on all level complexity clinical trial projects, often with major regulatory impact.
Florida Atlantic University
Boca Raton, FL
We are committed to providing educational programs, in partnership with our hospital affiliates, that enable our medical students and residents to become active, self-directed, life-long learners; equip our graduates to effectively treat the patients that they are most likely to encounter in their practices; produce graduates with the knowledge, skills, attitudes, and self-awareness required to practice effective, humanistic, patient-centered, evidence-based medicine; emphasize the centrality of collaborative relationships in the provision of the highest quality comprehensive health care; and foster and value collaboration among medical specialties, and between academic medicine and community health care professionals. Applicants meeting those criteria will be required to provide the following information before any offer of employment can be made: every institution of higher education attended; all previous employment since the applicant’s 18th birthday; list of all published material, current and pending research funding from any source, including details about the research, your role, funding source, and amount; list and description of any non-university professional activities; any affiliation with an institution or program in a foreign country.
Systimmune
Redmond, WA
It specializes in developing innovative cancer treatments using its established drug development platforms, focusing on bi-specific, multi-specific antibodies, and antibody-drug conjugates (ADCs). Collaborate with multidisciplinary teams on study initiation, data collection, database lock, delivery of statistical outputs and preparation of the study reports.
Emory Healthcare/Emory University
Atlanta, GA
Examples of ongoing projects include: + Optimizing selection of palliative radiation therapy techniques for patient outcomes and cost-effectiveness + Evaluating the role of federal housing assistance programs on palliative care and end-of-life care delivery + Value assessment of cancer-related interventions + Health policy evaluation, including the Affordable Care Act, pain-related policies, and Medicare payment reforms in patients with cancer + Racial disparities in cancer care delivery and outcomes MINIMUM QUALIFICATIONS: + A bachelor's degree in statistics, biostatistics, computer science, or a related field and two years related experience, OR an equivalent combination of education, training, and/or experience. + Works effectively within a group setting in areas of design of data collection instruments, study design, database management, statistical programming, analysis of data, statistical graphics, and writing of reports which include explanations of methods used and interpretation of results obtained.
Battelle Memorial Institute
Tampa, FL
Ability to gather, assemble, and analyze facts, draw conclusions, develop and utilize appropriate data collection techniques and data cleansing to produce valid and reliable findings, conduct analysis, devise recommended solutions, and package the entire process in briefings, papers, or reports suitable for top management use and decision-making. The Biostatistician/Operations Research & System Analyst serves as a recognized authority in designing and applying advanced mathematical and statistical models to evaluate and optimize human performance initiatives, advise on alternative courses of action, and ensure programs align with mission requirements and strategic objectives.
OQSIE
Cambridge, MA
This position is open within company's Rare Disease therapeutic area and provides the opportunity to contribute ongoing late phase studies as well as providing support on new and exciting clinical programs. Thorough and up-to-date knowledge of advanced clinical trial statistical methodology, including time-to-event and recurrent event analysis, sequential methods, longitudinal data analysis (e.g.
Medpace, Inc.
Cincinnati, Ohio
Responsibilities : Contribute to clinical development of plan preparation; Review of study protocol and preparation of statistical methodologies; Programming of study analysis, review of study results and preparation of statistical methods section for clinical / statistical reports; Communicate project requirements for CRF design, database design and database cleanup to ensure the key study variables are suitable for analysis; and. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective.
Rockefeller University
New York, New York
The salary of the finalist selected for this role will be set based on various factors, including but not limited to organizational budgets, qualifications, experience, education, licenses, specialty, and training. The University remains committed to its mission of improving the understanding of science for the benefit of humanity through both clinical and basic research in a diverse range of biological and biomedical issues.
Penfield Search Partners
PA or MA, PA or MA
In this role, you will contribute to the statistical strategy for clinical trials and regulatory submissions and support statistical activities across study design, data analysis, reporting, and submission preparation. Our client is an organization accelerating innovation to deliver greater impact for patients with Rare Diseases; their pipeline portfolio is diverse and ranges from early to late phase.
Penfield Search Partners
Fairfield, CT
This individual will play a key role in supporting ongoing and upcoming clinical programs in schizophrenia, bipolar disorder, and depression, contributing to study design, protocol development, and execution while working closely with cross-functional teams and external CRO partners. We are partnering with a growing biotech organization advancing multiple CNS programs and seeking a Senior Biostatistician who can operate both strategically and hands-on across Phase II studies.
Children's Hospital Los Angeles
$75712 - $129792
Los Angeles, CA
D level Biostatistician, and in collaboration with faculty investigators and CHLA research staff, performs statistical analysis and other tasks relevant to a biostatisticians role in support of qualitative and quantitative scientific research and evaluation projects. High-level familiarity with statistical analysis packages such as SPSS and SAS, and ability to utilize lower-level computational or programming languages such as R, S-Plus, VB, or C++ as necessary.
LLX Solutions
$80000 - $82000
Waltham, Massachusetts
Additionally, this position will support Project Directors in the production and presentation of Data Monitoring Committee reports, analyzing data for regulatory submissions and publications, and communicating with clients and team members if desired. Position Overview:The Biostatistician may review protocols and case report forms, perform sample size calculations, write Statistical Analysis Plans, develop and produce interim and final reports.
The EMMES Corporation
Rockville, undefined
At Emmes, your actions and hard work will have a direct impact on public health initiatives, both globally and in our local communities with opportunities for volunteerism through our Emmes Cares community engagement program. Emmes Group was founded as Emmes more than 47 years ago, becoming one of the primary clinical research providers to the US government before expanding into public-private partnerships and commercial biopharma.
The EMMES Corporation
Rockville, undefined
Oversees statistical activities and deliverables across a project or platform of related clinical research studies, leads a team of Statisticians and SAS Programmers and ensures that statistical deliverables are completed in a timely manner and with high quality. Responsibilities: Manages a team of Statisticians and SAS Programmers and is ultimately responsible for statistical deliverables across multiple projects or platforms of related clinical research studies.
Geisinger
Danville, PA
Through its 11 hospital campuses, the Geisinger Health Plan, and the Geisinger College of Health Sciences, which includes the Clinical Education Institute and Research Institute, the Geisinger Commonwealth School of Medicine (GCSOM), and the Geisinger School of Nursing, Geisinger serves more than 1 million residents throughout 46 counties in central, south-central, and northeastern Pennsylvania. The ideal candidate will have expertise in field(s) related to biostatistics, epidemiology, health economics, and/or health services research in a healthcare, academia, or industry setting, as well as strong methodological training in causal inference using non-randomized (quasi-experimental and observational) study designs.
Cook Group
West Lafayette, IN
Acquire and maintain Cook Mastery Level of Artificial Intelligence competency, including the ability to assess feasibility and risk of AI use cases, design or coordinate workflow-level AI solutions, guide teams on responsible AI governance, mentor others, and contribute to organizational policies and ethical decision-making. The followng qualifications are preferred: Strong understanding of clinical study design: power and sample size calculations, Type I error control, statistical analysis planning, and interpretation of results, across a variety of study designs including RCTs, performance goals and real-world evidence.
Truvian Sciences
San Diego, CA
You will work cross-functionally with teams in product development, regulatory affairs, scientific affairs, and marketing, playing a pivotal role in validating Truvian’s blood testing technology for market readiness. We are developing a fully automated benchtop system that delivers lab-accurate results from a small blood sample under 30 minutes—designed for use in retail clinics or private practice settings.
Pharmavise Corporation
Indianapolis, IN
E-Verify Participation: Pharmavise Consulting Corporation participates in E-Verify and will provide the federal government with your Form I-9 information to confirm that you are authorized to work in the U.S. If E-Verify cannot confirm that you are authorized to work, Pharmavise is required to give you written instructions and an opportunity to contact Department of Homeland Security (DHS) or Social Security Administration (SSA) so you can begin to resolve the issue. Key Responsibilities: Collaborate with clinical and regulatory teams to design statistically sound clinical trials (e.g., sample size calculation, randomization methods).
The EMMES Corporation
Rockville, undefined
Collaborates with clinical investigators to determine study design, contributes to protocol development, writes statistical analysis plans, performs statistical analysis, makes statistical inference and writes and presents reports summarizing findings including publications in peer-reviewed journals. At Emmes, your actions and hard work will have a direct impact on public health initiatives, both globally and in our local communities with opportunities for volunteerism through our Emmes Cares community engagement program.
The EMMES Corporation
Rockville, undefined
Collaborates with clinical investigators to determine study design, contributes to protocol development, writes statistical analysis plans, makes statistical inference, and writes and presents reports summarizing findings including publications in peer-reviewed journals. Generates study reports to be distributed to internal and external monitoring committees and regulatory bodies including, but not limited to, Data and Safety Monitoring Board reports, IND annual reports, and Clinical Study reports.
Systimmune
Redmond, WA
It specializes in developing innovative cancer treatments using its established drug development platforms, focusing on bi-specific, multi-specific antibodies, and antibody-drug conjugates (ADCs). Provide data-driven insights and statistical support to clinical teams, offering guidance on data-related challenges and participating in project team meetings as needed.
EXACT SCIENCES CORPORATION
MADISON, WI
statistics function on project teams for product development programs, providing strategic input and contributing significantly to the design. This role directly partners with thought leaders in the design, analysis, reporting, and internal publication of reports pertaining to.
Penfield Search Partners
Seattle, WA
Build and maintain reproducible data science communication products including interactive dashboards, analytic reports, and other deliverables that effectively communicate complex findings to diverse stakeholders. Experience with building and deploying interactive dashboards, reports, and other analysis dissemination tools using appropriate technologies (R Markdown, Jupyter notebooks, Shiny, Dash, streamlit etc.).
Dignity Health
$35.62 - $52.99
Phoenix, AZ
Joseph's includes the internationally renowned Barrow Neurological Institute (https://www.barrowneuro.org/) , Norton Thoracic Institute (https://www.dignityhealth.org/arizona/norton-thoracic-institute) , Cancer Center at St. Joseph's (https://www.dignityhealth.org/arizona/locations/stjosephs/services/university-of-arizona-cancer-center) , Ivy Brain Tumor Center (https://www.ivybraintumorcenter.org/) , and St. Our administrative data studies primarily use Medicare data to understand risk factors for neurologic diseases, to develop predictive models to identify patients earlier in their disease course, and to identify potential disease-modifying therapies using pharmacoepidemiology.
Beth Israel Lahey Health
Boston, MA
Customer Service: Ability to provide a high level of customer service to patients, visitors, staff and external customers in a professional, service-oriented, respectful manner using skills in active listening and problem solving. This role includes key statistician responsibilities including statistical design, and conducting analyses and data exploration, and generating key documents such as statistical analysis plans and grant materials for both observational studies and clinical trials.
The EMMES Corporation
Rockville, undefined
Providing support to the Therapeutic and Research Units, Business Development, Proposal, and Pricing Departments to appropriately resource and price new business opportunities for tasks within the scope of the Biostatistics Department. At Emmes, your actions and hard work will have a direct impact on public health initiatives, both globally and in our local communities with opportunities for volunteerism through our Emmes Cares community engagement program.
Otsuka America Pharmaceutical Inc.
Olympia, WA
Minimum $169,222.00 - Maximum $253,000.00, plus incentive opportunity: The range shown represents a typical pay range or starting pay for individuals who are hired in the role to perform in the United States. + Effective communications within biostatistics function and with study team and key stakeholders across different functional areas such as clinical, regulatory affairs, asset management, safety and clinical operation.
MUSC
Charleston, South Carolina
In particular, the statistician will play an important role in drafting or confirming that the methods section of the paper and statistical approaches are communicated in an accurate manner. 25% - Critically reviewing and co-authoring scientific manuscripts: The statistician will be acknowledged as a co-author on presentations and manuscripts resulting from their analyses.
Relay Therapeutics
$154000 - $250000
Cambridge, MA
Built on unparalleled insights into protein motion and how this dynamic behavior relates to protein function, we aim to effectively drug protein targets that have previously been intractable, with an initial focus on enhancing small molecule therapeutic discovery in targeted oncology. You will be an integrated member of the Relay Tx clinical development team, responsible for the in-house biostatistics expertise for the execution of clinical studies that will translate Relay's innovative science into impactful medicines for patients.
Pfizer
$169700 - $282900
New York City, NY
As a key member of project team, this position will interact directly with Clinical (Clinicians), Clinical Pharmacology, Statistical Programming, Data Management, Regulatory Strategy and Operations, Medical, Outcomes Research, Commercial, Operations and contract organizations supporting project deliverables. Provide planning and communication of statistical analyses, data presentations and scientific reports, including clinical trial results, exploratory analyses and analyses that synthesize results across studies, support for publication activities, scientific presentations and support for product defense.
Pfizer
$139100 - $231900
Bothell, WA
PREFERRED QUALIIFICATIONS** - Oncology experience - Strong statistical research and simulation skills and experience - Candidate demonstrates a breadth of diverse leadership experiences and capabilities including: the ability to influence and collaborate with peers, develop and coach others, oversee and guide the work of other colleagues to achieve meaningful outcomes and create business impact. - Perform the analyses of clinical trial data, provide statistical interpretation of results, and collaborate on the reporting of clinical trial results to regulatory authorities and the scientific community by contributing to the clinical study reports, clinical publications, conference posters and presentations.
Penfield Search Partners
San Francisco, CA
They are currently seeking a highly skilled and experienced Associate Director of Biostatistics to provide leadership to develop and execute statistical strategy, design and analyses for clinical trials in all phases. Please Have: MS/MA degree in related discipline and a minimum of 9 years of related experience; or, PhD in related discipline and a minimum of 5 years of related experience; or, Experience in Oncology and study Phases I-III highly preferred.
Pfizer
$169700 - $282900
New York City, NY
As a key member of project team, this position will interact directly with Clinical (Clinicians), Clinical Pharmacology, Statistical Programming, Data Management, Regulatory Strategy and Operations, Medical, Outcomes Research, Commercial, Operations and contract organizations supporting project deliverables. Provide planning and communication of statistical analyses, data presentations and scientific reports, including clinical trial results, exploratory analyses and analyses that synthesize results across studies, support for publication activities, scientific presentations and support for product defense.
Xeris Pharmaceuticals, Inc.
$140000 - $240000
undefined, undefined
Oversees the review of statistical documents and operational activities outsourced to CROs ensuring adherence to cost, timeline, and data quality requirements to ensure that the analysis plans use the most appropriate statistical methods and that the data displays such as tables/figures/listings are accurate and complete. Overview: The Associate Director, Biostatistics and Statistical Programming will drive biostatistical activities, performed primarily by vendors, in support of project timelines and budgets related to drug product development at Xeris.
Arrowhead Pharmaceuticals
$145000 - $190000
Los Angeles, CA
Arrowhead is leading the field in bringing the promise of RNAi to address diseases outside of the liver, and our clinical pipeline includes disease targets in the liver and lung with a promising pipeline of preclinical candidates. As an internal expert in biostatistics, you will provide technical leadership and biostatistical input to closely collaborate with other functional teams at Arrowhead, including Clinical Development and Operations, Regulatory, Commercial, Program Management and others.
Temple Health
Philadelphia, PA
This senior role provides strategic direction and operational oversight for biostatistics across FCCC, enabling high-impact, collaborative research and the effective use of innovative statistical and computational approaches throughout the Center’s diverse research programs. Temple Health consists of Temple University Hospital (TUH), Fox Chase Cancer Center, TUH-Jeanes Campus, TUH-Episcopal Campus, TUH-Northeastern Campus, Temple Physicians, Inc., and Temple Transport Team.
Fox Chase
Philadelphia, PA
This senior role provides strategic direction and operational oversight for biostatistics across FCCC, enabling high-impact, collaborative research and the effective use of innovative statistical and computational approaches throughout the Center’s diverse research programs. Temple Health consists of Temple University Hospital (TUH), Fox Chase Cancer Center, TUH-Jeanes Campus, TUH-Episcopal Campus, TUH-Northeastern Campus, Temple Physicians, Inc., and Temple Transport Team.
Albert Einstein College of Medicine
Bronx, New York
Biostatistics faculty collaborate widely across the institution; teach in the medical and graduate educational programs; and lead and participate in biostatistics resources in the ICTR, Montefiore Einstein Comprehensive Cancer Center, Center for AIDS Research, Einstein Aging Study, and other research programs. The Division of Biostatistics in the Department of Epidemiology and Population Health includes more than 20 faculty members with active research programs in clinical trials methodology, statistical genetics and genomics, epidemiologic methods, machine learning, and analysis of real-world data.
Cellectis
$220000 - $240000
New York, NY
In collaboration with functional leads, ensure that the execution of clinical trials, (specifically data capture, cleaning) delivers quality and timely ongoing and final databases, develop strategies to minimize the cost of clinical trial execution in delivering quality clinical trial data and ensure that clinical trial systems used in the running of clinical trials are effectively linked to avoid conflicting information. Minimum 15 years of experience in leading biostatistics in clinical research (at various levels and in different capacities), including having built the biostatistics function and 5 years managing a biostatistical group working on all phases of clinical research and drug development.
MUSC
Charleston, South Carolina
Derived datasets will be created by the biostatistician, validation of analyses and programs will be conducted and reports that includes tables and figures, descriptions of methods used, and interpretations of results will be included. This will include working with the protocol lead statistician and clinicians on proposals in which analysis plans are described, sample size justifications are proposed, and results are presented in a clear and transparent manner for interpretation by the appropriate audience.
TalentBurst, Inc.
Andover, MA
Collaborate with clinical operations, data, medical affairs, and clinical strategy teams to define study type, endpoints, estimands, and analysis frameworks that are robust, transparent, and fit for regulatory. impact/complexity studies and provides program-level and technical leadership across all statistical activities in the business unit.
MUSC
Charleston, South Carolina
25% - Utilize data management system to maintain participant records, track recruitment progress and study milestones, and generate recruitment and study visit reports for PI and the study team of the ECHO program at MUSC. Physical Requirements: (Note: The following descriptions are applicable to this section: Continuous - 6-8 hours per shift; Frequent - 2-6 hours per shift; Infrequent - 0-2 hours per shift) Ability to perform job functions in an upright position.
University of Alabama at Birmingham
Birmingham, AL
The ideal candidate will provide expert leadership in statistical methodology, study design, and data analysis across a range of research projects focused on cardiovascular genetics, proteomics, clinical trials, and computational medicine. By integrating rigorous biostatistical approaches with innovative clinical and translational science, the Lead Biostatistician will play a vital role in advancing precision medicine and improving patient outcomes.