44 Results for

Biostatistics Jobs in East Boston, MA

Jobs

New!

Burlington, MA5 days ago

specific responsibilities while upholding our core working behaviors of Trust and Respect, Communication and Feedback, Accountability and Reliability, Objectivity, and Team Balance and. •Provide high-quality statistical support across clinical programs, ensuring scientific.

Boston, MA30+ days ago

$180,000–$240,000 Per Year

Salary Range: CHI: $180,000-$240,000 USD NYC/SF: $190,000-$260,000 The expected salary range above is applicable if the role is performed from California and may vary for other locations (Colorado, Illinois, New York). We are seeking a highly motivated and capable Director of Biostatistics to lead a team of biostatisticians involved in multiple aspects of clinical research at Tempus.

Cambridge, MA30+ days ago

$185,000–$260,000 Per Year

Beam's suite of gene editing technologies is anchored by base editing, a proprietary technology that is designed to enable precise, predictable and efficient single base changes, at targeted genomic sequences, without making double-stranded breaks in the DNA. The ideal candidate will work closely with the Head of Biometrics and play a key role in the statistical strategy for clinical development programs and provide oversight to CROs to ensure timely execution of the clinical trials.

Watertown, MA30+ days ago

$195,000–$275,000 Per Year

Having advanced the first degrader into the clinic for immunological diseases, Kymera is focused on building an industry-leading pipeline of oral small molecule degraders to provide a new generation of convenient, highly effective therapies for patients with these conditions. As the Lead Statistician, you will spearhead the statistical efforts of a clinical program, playing a key role in the clinical development plan, regulatory submissions, and overall data strategy.

Watertown, MA30+ days ago

$195,000–$275,000 Per Year

Having advanced the first degrader into the clinic for immunological diseases, Kymera is focused on building an industry-leading pipeline of oral small molecule degraders to provide a new generation of convenient, highly effective therapies for patients with these conditions. How you'll make an impact: As the Lead Statistician, you will spearhead the statistical efforts of a clinical program, playing a key role in the clinical development plan, regulatory submissions, and overall data strategy.

Boston, Massachusetts30+ days ago

The Director will work closely with Clinical Development and external partners to drive trial design, analysis strategies, and regulatory‑ready outputs while remaining directly involved in study‑level statistical activities. Overview: The Director of Biostatistics is a hands‑on statistical leader responsible for the design, analysis, and interpretation of Phase 1–Phase 3 clinical trials with a primary focus on inflammation and oncology indications.

Cambridge, MA30+ days ago

Research: Support the development of research papers for statistical, machine learning, and medical journals on modern methodological approaches relevant to the company's interests and computing platform development, as well as applied papers growing out of consulting projects or conference interactions. PhaseV is a Boston-based technology company that redefines clinical development at scale with its enterprise-ready, multi-modal AI/ML platform — accelerating decisions, de-risking trials, and driving more efficient portfolio strategies.

Boston, MA30+ days ago

Ensure the accuracy, integrity, and consistency of statistical analyses across clinical development programs, from Phase I through regulatory submissions and post-approval activities. In this leadership role, you will oversee the development, execution, and interpretation of statistical analyses, maintaining data quality, analysis integrity, and compliance with regulatory requirements.

Boston, MA30+ days ago

$230,000–$250,000 Per Year

Reporting to the Head of Biometrics, this individual will serve as Vors global expert in biostatistical science, with accountability for all aspects of clinical trial design, statistical methodology, regulatory submission deliverables, and cross-functional scientific partnership. Regulatory Affairs & Submission Leadership • Author and review statistical sections of regulatory documents including INDs, investigator brochures, briefing books, CSRs, and eCTD/CTD module submissions to FDA, EMA, and other health authorities.

Boston, MA30+ days ago

As a global biotherapeutics leader, they develop innovative therapies across immunology, hematology, cardiovascular, metabolic, respiratory, and transplant medicine—leveraging cutting-edge platforms including plasma fractionation, recombinant protein technology, and cell & gene therapy. Our client is a global biopharma company looking for two Directors, Biostatistics to lead statistical strategy across clinical programs and drive excellence from study design through regulatory submission.

Cambridge, MA30+ days ago

$228,000–$245,000 Per Year

This role combines scientific depth, regulatory rigor, and operational execution to ensure the design, analysis, and interpretation of clinical trials support efficient development and high-quality regulatory submissions. The Director serves as a key partner to Clinical Development, Clinical Operations Data Management, Regulatory Affairs, Medical Affairs and while building scalable biostatistics capabilities appropriate for a growing organization.

Cambridge, MA30+ days ago

$154,000–$250,000 Per Year

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.

Cambridge, MA30+ days ago

$301,800–$408,200 Per Year

Lead the development and implementation of statistical strategies across programs including clinical trial designs, endpoint strategies, and regulatory strategies, partnering with Clinical Development and cross-functional leaders to shape development plans. The Executive Director leads a team of statisticians and works closely with cross‑functional leaders to ensure rigorous and innovative quantitative approaches to drug development.

Boston, MA30+ days ago

$236,000–$354,000 Per Year

General Summary: The Associate Director, Biostatistics will perform sophisticated scientific statistical analyses in support of the company's Global Medicines Development and Affairs area with minimal guidance and mentoring on new and complex issues. At Vertex, our Total Rewards offerings also include inclusive market-leading benefits to meet our employees wherever they are in their career, financial, family and wellbeing journey while providing flexibility and resources to support their growth and aspirations.

Boston, MA30+ days ago

General Summary: The Director, Biostatistics will independently perform highly scientific statistical functions in support of the company's Global Medicines Development and Affairs (GMDA) area on new and complex issues. At Vertex, our Total Rewards offerings also include inclusive market-leading benefits to meet our employees wherever they are in their career, financial, family and wellbeing journey while providing flexibility and resources to support their growth and aspirations.

Boston, MA30+ days ago

Remote

$180,000–$215,000 Per Year

Provide statistical support on one or more assets or indications by directing the execution of statistical analyses, review of statistical outputs, and ensuring accurate results interpretation, collaborating closely with physicians, evidence generation stakeholders, or other cross-functional leads as appropriate on the interpretation of clinical results. Provide guidance to the clinical, regulatory, and/or evidence generation teams on conclusions and inferences from the data package, ensuring statistical perspective is integrated into regulatory and external meetings, and delivering data packages aligned with submission requirements or key decision-making.

Boston, MA19 days ago

The position involves hands-on technical leadership and requires comprehensive and detailed knowledge of statistical programming languages and software, filing support, clinical trial databases, and the drug development process. The role oversees external CRO partners to ensure high-quality, timely, and compliant delivery of analysis datasets, tables, listings, and figures that support clinical development and regulatory submissions.

Boston, MA19 days ago

Cambridge, MA30+ days ago

$155,000–$225,000 Per Year

Manage the activities of data summary, statistical analysis, patient profile, safety and efficacy tables, listings and figures using Base SAS, SAS Macros, SAS/STAT, SAS/Graph, SAS/SQL, SAS/ODS and R. Beam's suite of gene editing technologies is anchored by base editing, a proprietary technology that is designed to enable precise, predictable and efficient single base changes, at targeted genomic sequences, without making double-stranded breaks in the DNA.

Boston, MA23 days ago

Remote

Full-time

Leads projects (all phases and even a program of studies) and smaller submissions, manages client meetings, CRMs, collaborates well with regulatory, PMs and sponsor. With a global footprint across four continents, MMS not only maintains an industry-leading customer satisfaction rating but also fosters a collaborative and inclusive work environment where employees can thrive.

Boston, Massachusetts9 days ago

Strong quantitative training, experience applying statistical methods in health or clinical research settings, and an interest in advancing rigorous, equity-centered research related to food, nutrition, and health that has real-world impact and makes a difference in people’s lives. Document and maintain reproducible analysis workflows, including well-annotated statistical code, version-controlled scripts, clear data dictionaries, and organized file structures that support transparency and replication.

Waltham, Massachusetts30+ days ago

$80,000–$85,000

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.

Boston, MA30+ days ago

Remote

Full-time

Produce and present external company presentations providing industry visibility for the organization; Continually suggesting solutions to solve issues in tune with organizational direction. Lead complex projects, programs and submissions, manages client meetings, CRMs, collaborates well with regulatory, PMs and sponsors.

Cambridge, MA30+ days ago

In this role, you will work closely with Clinical Research, Global Patient Safety and Risk Management (GPSRM), Regulatory Affairs, and Biostatistics to inform clinical development and answer product- and disease-area research questions for Alnylam RNAi therapeutics using observational studies and real-world evidence. The Director Epidemiology is responsible for representing the Epidemiology function at Alnylam, providing expertise, strategic vision, and oversight of epidemiology and real-world evidence (RWE) activities in support of all clinical development programs and marketed RNAi therapeutics.

Boston, MA30+ days ago

$114,000–$211,600 Per Year

In addition to supporting regulatory submissions, the ADS Programmer plays a critical role in generating data insights through platforms such as the Insight Engine, enabling real-time exploration and interpretation of diverse clinical and exploratory data. We identify, influence, and adopt industry-leading digital and automation solutions, develop analytical approaches to support exploratory analyses, and align statistical programming practices across both early- and late-stage clinical development.

Watertown, MA30+ days ago

$160,000–$240,000 Per Year

Having advanced the first degrader into the clinic for immunological diseases, Kymera is focused on building an industry-leading pipeline of oral small molecule degraders to provide a new generation of convenient, highly effective therapies for patients with these conditions. Manage multiple tasks, troubleshoot technical and project issues, and assist with the infrastructure development of the department; Evaluate and implement innovative tools and programming technologies to streamline processes and improve team efficiency and quality.

Cambridge, MA30+ days ago

Manages the activities of data summary, statistical analysis, patient profile, safety and efficacy tables, listings and figures using Base SAS, SAS Macros, SAS/STAT, SAS/Graph, SAS/SQL, SAS/ODS and R. The senior manager will be responsible for developing and maintaining statistical programming functions within a therapeutic area to support various clinical studies and submissions to ensure successful execution for Beam's clinical programs.

Cambridge, MA30+ days ago

Remote

This individual will work collaboratively cross-functionally to provide hands-on data management support, programming support and technical leadership to develop, maintain, validate the clinical database, and run computer programs that access, visualize, and report clinical trial data, in accordance with various clinical plans, ICH guidelines, and applicable regulatory requirements. • Supports leading data management activities (i.e. DMP creation, CRF creation, edit checks creation, database lock), assisting with database setup, conduct and closeout phases.

Cambridge, MA30+ days ago

$144,400–$189,400 Per Year

Essential Duties & Responsibilities: Develop, validate and maintain analysis-ready datasets, tables, figures and listings for observational and RWE studies derived from diverse real-world data sources, including claims, electronic health records (EHRs) and registry data. Write, test and validate programs to produce analysis datasets, TLFs and presentation output, to be included in reports for submission to regulatory agencies, publications and other communications as needed.

Cambridge, MA30+ days ago

$155,000–$190,000 Per Year

Manages the activities of data summary, statistical analysis, patient profile, safety and efficacy tables, listings and figures using Base SAS, SAS Macros, SAS/STAT, SAS/Graph, SAS/SQL, SAS/ODS and R. Beam's suite of gene editing technologies is anchored by base editing, a proprietary technology that is designed to enable precise, predictable and efficient single base changes, at targeted genomic sequences, without making double-stranded breaks in the DNA.

Boston, Massachusetts30+ days ago

Employee

Cambridge, MA30+ days ago

The Farhat Lab in the Department of Biomedical Informatics is seeking a highly motivated 'dry lab postdoctoral research fellow interested in pursuing innovative studies in the field of infectious disease genomics and its translation to the clinic. Salary Range Information regarding postdoctoral fellow salary which is determined by the number of years post PhD can be found at http://postdoc.hms.harvard.edu/guidelines.

Boston, MA30+ days ago

Typically leading 2 program teams and drive the successful execution of clinical studies / programs / research strategies; define and manage the benefit to risk profile of our products Representing Clinical Development on the Global Program Team (GPT) and Global Medicine Team in presentations at management and review committees (e.g., Clinical Document Review Committee, Development and Commercial Steering Committee); advance understanding of the impact our therapies have on the pathophysiology of rare and orphan diseases through scientific discourse and interpretation of data Fostering development of Medical Directors and CDS and/or fellows. or equivalent 7+ years of experience in clinical development; clinical research, global regulatory, and product development expertise Has prepared documents and attended regulatory meetings with FDA and other regulatory agencies Experience designing and executing multinational clinical trials required Demonstrated ability to lead cross-functional teams to define clinical strategy and clinical study design Experience supporting business development activities M.D.

New!

Boston, MA3 days ago

The Wastewater Epidemiology Fellow will coordinate with internal and external partners to integrate data from the Wastewater Monitoring Program with other public health surveillance data to enhance awareness, preparedness, and response to infectious disease. The Boston Public Health Commission does not have a laboratory and contracts with third-party laboratories to perform analyses and third-party technicians to collect wastewater, so this is not a laboratory or field-work position.

Waltham, MA30+ days ago

Primary Responsibilities: Informing development strategies from HEOR / market access perspective Represent the HEOR and market access perspective in internal clinical development and regulatory forums Provide critical input into clinical development plans, including protocol design, endpoint selection, and other aspects of clinical trial evidence generation, to ensure alignment with future payer and HTA expectations Communication of value to payers and HTA bodies Lead development of AMCP dossiers for US payers Lead development of cost-effectiveness models for NICE and other HTA bodies requiring formal cost-effectiveness analyses Serve as a core team member for HTA submissions outside the US, with responsibility for shaping and stress-testing value narratives included in pricing and reimbursement dossiers and interpreting and recommending evidence to support such narratives, in a way that optimizes both credibility and relevance for payer decision-making Make substantial contributions to other payer communication materials (e.g., Medical Value Liaison slide decks) and launch readiness activities as needed Leading real-world evidence strategy and execution of real-world analyses Lead planning of real-world evidence generation activities to address evidence gaps as needed for informing decision-making by payers, HTA bodies, and clinicians Oversee execution of real-world data analyses, ensuring analytical rigor and fitness for purpose Interpret and translate results from real-world analyses into peer-reviewed publications and other external communications intended to meaningfully inform clinical practice and payer/HTA decision-making. Accordingly, the Director, Global HEOR, helps shape development plans, evidence strategies, and value narratives so that they align with how payers and health technology assessment (HTA) bodies make decisions, balancing analytical rigor with a clear focus on what is relevant for decision-making.

Boston, MA22 days ago

$280,895.20–$421,342.80 Per Year

You will be responsible for: Serve as subject medical expert and clinical development leader accountable for 2 (or more) programs, including but not limited to the preparation and execution of a clinical development strategy and related documents including protocols, charters, statistical summary reports, meeting presentations, publications, and clinical sections of regulatory documents. This is a therapeutic area role and is specifically designated to provide medical leadership and input to Program Teams across drug development (i.e., transitioning molecule through IND/CTA and First in Human study stage to Proof of Concept /Phase2 stage, Phase 3 and regulatory approval ).

Boston, MA30+ days ago

Remote

Full-time

Working alongside innovative statisticians you will be responsible for leading the full life-cycle of KerusCloud support and statistical services, from: Assisting customers with their study design with a particular focus on simulation with KerusCloud to ensure they are aligned with the study objectives. As part of our Strategic Statistical Services Arm, this is a full-time role with emphasis on being an internal and external SME for clinical trial design, together with providing consultation to advise clients on a range of broader statistical issues, and will have an internal job title of Strategic Statistician.

Boston, MA21 days ago

This requires experience working with databases, establishing data connections and running queries, aggregating and synthesizing data for business plans, trends, and projections, along with creativity, curiosity, and initiative to evolve the tools and reporting systems to meet the priorities of a dynamic healthcare environment. Strong experience in data management and analytic tools and techniques; Strong experience in report writing, analytics, visualizations, dashboard creation; Strong experience demonstrating analytical, financial, qualitative and quantitative skills.

Cambridge, MA30+ days ago

$260,000–$320,000 Per Year

Provide operational oversight of Medical Affairs evidence generation, including vendor/CRO governance, milestone/deliverable tracking, data‑quality plans, risk management, and on‑time execution across Medical Affairs–led studies; contribute to long‑term capability building (digital health, real‑world studies). Support business decisions around ex-US strategy including, but not limited to, scoping ex-US opportunities, prioritizing country engagement, early scientific advice / parallel consultations with EMA and HTA bodies (e.g., HTACG/JSC), providing advice to development programs on endpoint selection to support product and reimbursement approvals ex-US, etc.

New!

Marlborough, MA3 days ago

This incumbent will be operating with a high degree of autonomy, this individual will shape fit-for-purpose RWD strategies, evaluate and operationalize external data assets, and lead advanced analytics initiatives using EHRs, claims, registries, and linked healthcare data. About the role: The Principal Data Strategist, Real World Evidence (RWE) will lead enterprise real-world data (RWD) strategy and advanced analytics initiatives that support scalable, regulatory-aligned evidence generation across Boston Scientific.

Cambridge, MA30+ days ago

$175,000–$220,000 Per Year

Strategic thinker, planner and implementer of computational biomarker and translational analyses for early‑phase oncology studies (e.g., FOG‑001 and ERG/AR degraders), from IND‑enabling work through Phase 1/2, ensuring continuity between preclinical and clinical datasets. Design and execute analysis plans for diverse biomarker modalities across preclinical models and clinical samples, including bulk and single‑cell RNA‑seq, DNA panels/WES, ctDNA, IHC/IF, multiplex protein assays, and other exploratory readouts.

New!

Hanscom AFB, MA5 days ago

$84,579–$109,959 Per Year

FOREIGN EDUCATION: If you are using education completed in foreign colleges or universities to meet the qualification requirements, you must show the education credentials have been evaluated by a private organization that specializes in interpretation of foreign education programs and such education has been deemed equivalent to that gained in an accredited U.S. education program; or full credit has been given for the courses at a U.S. accredited college or university. Related Degree: Bachelors degree in a branch of engineering, physical science, or life science that included 12 semester hours in chemistry, including organic chemistry, and 18 additional semester hours of courses in any combination of chemistry, physics, engineering, health physics, environmental health, biostatistics, biology, physiology, toxicology, epidemiology, or industrial hygiene.

Boston, MA30+ days ago

$90,000–$135,000 Per Year

Real World Data Expertise: Lead the derivation of complex real-world endpoints using extensive coding, demonstrating deep comprehension of Tempus clinical and molecular data structures and complexity, while also serving as an expert on the methodological nuances and limitations of real-world data. Methodology & Platform Contribution: Stay up-to-date on methodological advancements in real-world studies (e.g., causal inference, survival analysis) and oncology guidelines (NCCN and ongoing clinical trials) to contribute to reusable code, internal packages, and best practices that can be applied across multiple collaborations.

New!

Boston, MA3 days ago

Summary: Following established policies, procedures, and study protocols, provides assistance on clinical research studies, including recruiting, evaluating, and consenting patients for studies; collecting and organizing patient data; scheduling patients for study visits; performing clinical tests such as phlebotomy, EKGs, etc. and maintaining and updating data generated by the study. The research coordinator's primary responsibility in the MGH Diabetes Research Center will be working on studies related to pregnancy and/or diabetes including those that use oral glucose tolerance testing and continuous glucose monitoring and collect biospecimens.

Resume Resources

Free Resume Templates Free Resume Builder

Get noticed by top employers!

Upload your resume to let employers know you're open to Biostatistics job opportunities. Plus, receive relevant job recommendations in your inbox.

Create A Free Account

Biostatistics Jobs in East Boston, MA

Associate Director, Biostatistics Clinical Dynamix, Inc.

Director, Biostatistics Tempus AI Inc

Associate Director/Director, Biostatistics Beam Therapeutics

Director of Biostatistics Kymera Therapeutics

Director, Biostatistics Kymera Therapeutics Inc

Director, Biostatistics Monte Rosa Therapeutics, Inc

Biostatistics Researcher PhaseV

Senior Director, Biostatistics CEDENT

Director, Biostatistics Vor BioPharma Inc

Director Biostatistics Penfield Search Partners

Director, Biostatistics Avalyn Pharma

Associate Director / Director, Biostatistics Relay Therapeutics

Executive Director Biostatistics Alnylam Pharmaceuticals Inc

Biostatistics Associate Director Vertex Pharmaceuticals Inc

Biostatistics Director (Hybrid) Vertex Pharmaceuticals Inc

Associate Director, Biostatistics Les Laboratoires Servier SAS

Lead statistical Programmer Katalyst Healthcares & Life Sciences

Lead statistical Programmer Karwell Technologies

Sr. Manager/AD, Statistical Programmer Beam Therapeutics

Senior Biostatistician - Remote (US) MMS

Biostatistician - Friedman School of Nutrition Tufts University

Biostatistician LLX Solutions

Principal Biostatistician - Remote MMS

Director Epidemiology Alnylam Pharmaceuticals Inc

Senior ADS Programmer Genentech Inc

Associate Director, Statistical Programming Kymera Therapeutics

Senior Manager, Statistical Programming Beam Therapeutics Inc

Associate Director, Clinical Data Programmer Amylyx Pharmaceuticals Inc

Senior Manager, Scientific Programming BeOne Medicines Ltd

Senior Manager, Statistical Programming Beam Therapeutics

Strategy Insights & Planning Associate Consultant - HEOR Value and Evidence Communication ZS

HMS - Postdoctoral Fellow in Biomedical Informatics (Farhat Lab) Harvard University

Executive Medical Director, Hematology AstraZeneca Plc

Wastewater Fellowship BOSTON PUBLIC HEALTH COMMISSION

Director, Global Health Economics & Outcomes Research HEOR Dyne Therapeutics Inc

Senior Medical Director Clinical Development Neurology Alexion Pharmaceuticals Inc

Study Design Statistician (Remote) MMS

Healthcare Data Analyst (Clinic Administration) Joslin Diabetes Center

Senior Director, Global HEOR Beam Therapeutics

Principal Data Strategist, Real World Evidence (RWE) Boston Scientific Corp

Associate Director, Data Science, Computational Biology Parabilis Medicines

Industrial Hygienist U.S. Department of Defense

Data Scientist II, Real World Evidence (RWE), Pharma R&D Tempus AI Inc

Clinical Research Coordinator I Brigham and Women's Hospital

Resume Resources