Biostatistician Jobs in the United States
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.
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.
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.
Penfield Search Partners
Fairfield, CT
This role will focus on the design, analysis, and interpretation of clinical studies involving human subjects, with an emphasis on diagnostic device performance and sensitivity testing. The ideal candidate has prior experience working with medical device clinical data and can operate independently in a fast-paced, resource-lean environment.
Penfield Search Partners
$75 - $100
Fairfield, CT
The ideal candidate combines hands-on programming ability with statistical acumen, helping to structure and streamline complex, messy back-end data to support analytical workflows. This role requires someone who thrives in modern data environments — including PostgreSQL and Databricks — and understands how R fits into that ecosystem for analytics, simulation, and modeling.
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.
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.
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.
Cytel
Olympia, WA
Demonstrated experience in: + Leading Early phase clinical trials + Conduct safety analyses for phase 2/3 clinical trials + Sample size calculations and protocol concept development + SAP development and clinical study report preparation + Regulatory submissions (preferred) + Proven experience serving as an unblinded DMC. As a Principal Biostatistician, you will leverage advanced statistical methodologies to leading Phase 1 studies as well as conducting safety analyses for Phase 2/3 trials, with a particular focus on rare disease programs.
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.
Pharmavise Corporation
Indianapolis, MN
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).
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.
Statistics & Data Corporation (SDC)
Waltham, MA
Actively participate in writing statistical sections of protocols, preparing statistical analysis plans, preparing data deliverables for clinical study reports, interpreting analysis results, writing statistical sections of clinical study reports, and participating in meetings with drug regulatory agencies as required. · Typically a Master’s degree in biostatistics, statistics or other related, scientific field and four years of relevant professional experience; or a PhD in biostatistics, statistics or other related, scientific field and three years of relevant experience; or equivalent combination of experience, education, and/or demonstrated ability.
Cytel
Olympia, WA
Summary of Key Responsibilities + Leads statistical support for post approval value evidence generation and reimbursement submissions + Conducts post hoc analysis to support publications and presentations + Reviews and authors abstract, manuscript, regulatory documents + Collaborates with cross-functional team to support observational studies + Develops statistical sections of study protocols and statistical analysis plans. + Accountable for the collaboration with Statistical Programming to implement statistical analysis of all clinical trial, registry, observational and non-interventional data supporting Medical Affairs needs + Contributes to observational study reports and regulatory documents, e.g., DSURs, briefing documents, etc.
Edwards Lifesciences
$129000 - $182000
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. Edwards’ groundbreaking work in transcatheter aortic heart valve replacement (TAVR) pioneered an innovative, life-changing solution for patients by offering heart valve replacement without the need for open heart surgery.
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.
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.
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.
Cytel
$88800 - $133200
Olympia, WA
Axio Research, LLC seeks a Biostatistician in Seattle, WA to support teams of biostatisticians and statistical programmers in creating unblinded reports of confidential, ongoing clinical trial data for Data Monitoring Committees. Review and perform oversight of analysis plans, statistical analyses, outputs, and datasets provided by vendors.
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.
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.
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.
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.).
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.
Guidehouse
Atlanta, GA
Key ResponsibilitiesDesign and implement advanced statistical analyses, including time series analyses (e.g., interrupted time series), segmented regression, linear/logistic regression, hierarchical and longitudinal modeling. Note that Guidehouse will never charge a fee or require a money transfer at any stage of the recruitment process and does not collect fees from educational institutions for participation in a recruitment event.
Gan & Lee Pharmaceuticals
null, NJ
As a key member of the statistical department, this role will be responsible for biostatistical activities for Gan & Lee projects, including design, analysis, and presentation of data to advance new product development, domestic/international regulatory submissions, and lifecycle management of existing products. Develops statistical analysis plans and file/report specifications; determine appropriate statistical methodology for data analysis; reviews study setup activities including but not limited to randomization, CRFs and data edits.
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.
J.S. Held LLC
Redmond, WA
Our professionals serve as trusted advisors to organizations facing high stakes matters demanding urgent attention, staunch integrity, proven experience, clear-cut analysis, and an understanding of both tangible and intangible assets. This senior leadership role is designed for a highly accomplished professional who will drive strategic growth, expand client relationships, and lead complex pharmacoepidemiology engagements.
J.S. Held LLC
$90000 - $130000
Redmond, WA
Apply and deepen understanding of core consulting skills (client communication support, budgeting exposure, workflow management).Build cross-functional familiarity with toxicology, exposure science, industrial hygiene, and risk assessment by collaborating on multidisciplinary engagements. Our professionals serve as trusted advisors to organizations facing high stakes matters demanding urgent attention, staunch integrity, proven experience, clear-cut analysis, and an understanding of both tangible and intangible assets.
J.S. Held LLC
$130000 - $160000
Redmond, WA
Our professionals serve as trusted advisors to organizations facing high stakes matters demanding urgent attention, staunch integrity, proven experience, clear-cut analysis, and an understanding of both tangible and intangible assets. Held is a global consulting firm that combines technical, scientific, financial, and strategic expertise to advise clients seeking to realize value and mitigate risk.
Pharmaron
$110000 - $135000
Franklin Township, NJ
Founded in 2004, Pharmaron has invested in its people and facilities and established a broad spectrum of research, development, and manufacturing service capabilities throughout the entire drug discovery, preclinical, and clinical development process across multiple therapeutic modalities, including small molecules, biologics, and CGT products. We're proud of the impact we make and just last year, we supported over 780 discovery projects, 1,000+ CMC programmes, and 1,000+ clinical trials across all phases.
Penfield Search Partners
Washington, DC
Manage CRO statisticians and internal biostatistics team, including junior statistician, contract statistician and programming team in support of biostatistics operational activities. Develop and/or review statistical documents or deliverables for clinical trials including Statistical Analysis Plan (SAP) and integrated summaries of drug efficacy and safety, TFLs, interim analysis plan and others.
Otsuka Pharmaceutical Co.
Princeton, NJ
This is a strategic and critical role in the development of protocols and statistical designs in different phases of the clinical trials leading to approval of drug products in different phases of the clinical trials. 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.
Seneca Holdings
Atlanta, GA
Basic Qualifications: BA/BS with 0–3+ years of experience in epidemiologist, medical epidemiologist, statistician, biostatistician, bioinformatician, health science, laboratory analysis, laboratory training, virology, assay development, microbiology, or related field in a public health setting). This role involves providing epidemiological, statistical, surveillance, and research support to enhance public health responses to respiratory viruses, including COVID-19.
Summit Therapeutics Sub, Inc.
$184500 - $230000
Miami, FL
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. Serves as the project level biostatistician and provides leadership within biostatistics function to develop and execute statistical strategy, study design, statistical analyses, and regulatory submissions for clinical trials in oncology.
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.
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.
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.
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.
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.
Pfizer
$139100 - $225100
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.
Xeris Pharmaceuticals, Inc.
$140000 - $240000
Chicago, Illinois
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.
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.