Biostatistician, Regulatory Submissions (2026 Start Date)
$210k - $255kAnalysis Group
Biostatistician, Regulatory Submissions (2026 Start Date) Location: Boston, MA Job ID: 2026-2926 Type: Regular or Sign on Category: General Overview About Analysis Group's HEOR, Epidemiology, & Market Access Practice: Make an impact at Analysis Group, where we collaborate with our clients to develop and implement regulatory and analytical strategies to support life sciences products throughout their life cycles. Founded in 1981, Analysis Group is one of the largest international economics consulting firms, with more than 1,500 professionals across 15 offices, including more than 250 professionals who focus on health care. Analysis Group's health care experts apply analytical expertise in health economics and outcomes research (HEOR), clinical research, market access and commercial strategy, health care policy, epidemiology and drug safety, data science, and biostatistics. Analysis Group's internal experts, together with its network of affiliated experts from academia, industry, and government, provide our clients with exceptional breadth and depth of expertise and end-to-end consulting services globally. We draw upon our deep expertise to provide innovative, data-driven strategies for clients in the life sciences industry across all phases of product development and commercialization. We help our clients define markets, demonstrate value, and inform business decisions throughout product lifecycles. We have a broad range of expertise and collaborate with leading academics in our areas of expertise to offer cutting-edge analyses and analytical tools to address business and clinical challenges that require rigorous, evidence-based research. We are distinguished by the way we integrate our capabilities to provide our clients with a comprehensive approach to problem solving. We apply our analytical expertise to support pro bono initiatives that address critical public health and social issues. Our work includes collaborations with organizations such as GHESKIO in Haiti to develop digital tools that improve HIV clinic operations and patient outcomes, and Partners in Health in Lesotho to evaluate maternal and child health, HIV, and TB treatment outcomes. These efforts have been recognized by the Boston Bar Association's President's Award and highlighted at the International AIDS Society Conference, underscoring our commitment to using data and evidence-based research to advance global health and social impact . We have also been recognized as a best place to work in several top surveys, including national surveys by Glassdoor (Best Places to Work, Employees' Choice Award, small and medium business category) and Vault (17th overall in the Vault Consulting 50, and the top-ranked economic consulting firm). About the Biostatistician Position Analysis Group is seeking an experienced professional to support the continued growth of our clinical trial and biostatistics capabilities. This role is suited for candidates with a strong foundation in clinical trial data, statistical programming, and regulatory processes who are interested in applying their expertise in a consulting environment. Biostatisticians play a key role in leading analytical workstreams, guiding project teams, and contributing to strategic decision-making across a diverse portfolio of client engagements. Responsibilities Apply biostatistical methods to support clinical development, regulatory submissions (e.g., FDA, EMA), and evidence generation strategies. Contribute to strategic advising on clinical trial design, analysis strategy, and interpretation of results. Oversee implementation of statistical analysis plans (SAPs) and ensure high-quality, reproducible analytical outputs. Manage and mentor teams of analysts and associates, providing guidance on technical execution and professional development. Direct data integration, cleaning, and transformation efforts across clinical trial and real-world data sources. Develop tools, programming standards, and best practices to enhance efficiency and scalability of analyses. Communicate findings to technical and non-technical audiences, including translating complex analyses into clear, actionable insights. Contribute to business development efforts and support ongoing client relationships. Participate in dissemination of research through publications, presentations, and regulatory documentation. Qualifications Advanced degree (PhD preferred, Master's considered) in Biostatistics, Statistics, Epidemiology, or a related quantitative field. Approximately 35+ years of relevant experience in clinical trials, pharmaceutical, biotech, or CRO environments. Experience in early- to late-phase clinical trial design and regulatory evidence strategy. Experience supporting or contributing to clinical phase regulatory submissions for the US FDA and other regulatory authorities. Direct participation in regulatory interactions is a plus. Excellent judgement, problem-solving, and communication skills, with the ability to translate complex technical concepts into clear, structured insights for clients. While prior consulting experience is not required, candidates should demonstrate strong potential for client-facing work and structured problem solving. Prior experience collaborating across cross-functional stakeholders (e.g., clinical, regulatory, HEOR). Experience managing analyses, including SDTM, ADaM, and TLF development. Demonstrated ability to manage multiple workstreams and meet deadlines. Interest in mentoring and developing junior team members. Collaborative mindset and ability to work across interdisciplinary teams. While not required, a plus would be experience with post-marketing evidence generation, including label expansion strategies, PASS/PAES, Phase IV studies, and the use of real-world evidence to support regulatory decision-making. Candidates must be legally authorized to work in the United States at the time of hire. Analysis Group may consider candidates who require visa sponsorship, consistent with business needs. Analysis Group offers competitive compensation and a comprehensive benefits package. The estimated salary range for this position is $210,000 to $255,000. Compensation offered will be based on a number of factors including work experience, education, and skill level. This role is eligible for a discretionary annual bonus that is determined in large part by individual performance. To learn more about our benefit offerings, click here. Analysis Group embraces equal opportunity. We are committed to building teams that bring a variety of backgrounds, perspectives, and skills, as we believe that a strong and inclusive workforce directly supports our goal of providing the highest-quality work. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or any other class protected under applicable federal, state, or local law, and we encourage candidates of all backgrounds to apply. #J-18808-Ljbffr Analysis Group
- Analysis Group, Inc. is hiring a Biostatistician in Boston to support clinical trial analysis and decision-making. The successful... ...methods and manage analyst teams, with responsibilities in regulatory submissions and data integration. Preferred qualifications include an...Regulatory
- Analysis Group is seeking an experienced Biostatistician to support clinical trial and... ...expertise in clinical trial data and regulatory processes, engaging in meaningful client... ...applying biostatistics to support regulatory submissions. Join a diverse team committed to...Regulatory
$210k - $255k
Analysis Group, Inc. is seeking a Biostatistician to enhance its clinical trial and biostatistics capabilities. The role requires... ...will manage project teams, apply biostatistics methods for regulatory submissions, and communicate complex findings effectively. The...Regulatory- Analysis Group is seeking an experienced Biostatistician in Boston to support clinical trial and biostatistics capabilities. Candidates... ...skills in clinical trial data, statistical programming, and regulatory processes. The role involves leading analytical workstreams,...Regulatory
- ...Job Title Executive Director, Regulatory Operations and Submission Management Department Regulatory Affairs Reports To Head of Regulatory... ...and below, and/or matrixed Regulatory Affairs staff Date Prepared May 20, 2026 Job Summary The Executive Director, Regulatory Operations...Regulatory
$178k - $216k
...efficacy and safety summaries for New Drug Application (NDA) submissions Design analysis file specifications in accordance with the statistical... ...and guidance to junior level and new staff Understand regulatory requirements related to the specific therapeutic areas and...RegulatoryWork experience placement- ...found at: What You'll Do The Staff Biostatistician at the Food is Medicine Institute will... ...Support ongoing study tasks including IRB submissions, enrollment tracking, and interim... ...ensuring analyses align with ethical, regulatory, and sponsor requirements. The Staff Biostatistician...RegulatoryTraineeshipInterim roleShift work
$110k
A biostatistician applies statistical methods to health research designing studies that advance... ...trials and analyzing data to support regulatory approvals. Academic Institutions: Universities... ...fields can anticipate competitive starting salaries, typically ranging from $60,00...RegulatoryWork at officeWorldwide- ...our proven, scientific approach to complex trial data and regulatory submission challenges. With a global footprint across four continents... ...advance your career. Visit or follow MMS on LinkedIn. Senior Biostatistician: Responsibilities: Create randomization and kit...RegulatoryRemote job
- ...activities relating to design, delivery and interpretation, regulatory submissions and/or commercialisation. This individual is able to... ...problems, problem solving and quality focus Date Posted 16-Jun-2026 Closing Date 09-Jul-2026 Our mission is to build...Regulatory
- ...A biopharmaceutical company in Boston is seeking a Regulatory Affairs Specialist to coordinate the preparation of regulatory submission packages. The ideal candidate will have at least 8 years of experience in Regulatory Affairs, particularly with Small Molecule drugs...Regulatory
$24 - $30 per hour
...activities Role Type: Full‑time, 3‑month internship Start Date: We are currently recruiting for start dates in Summer 2026 and you will be asked to state your... ...economic models or health technology assessment submissions. You will typically be working on several projects...Hourly payPermanent employmentFull timeTemporary workSummer workInternshipWork at officeWork from homeFlexible hours1 day per week$1,141 per week
...Contract Duration: 13 Weeks Start Date: 7/13/2026 About the Position ID: 772766... ...Comments and coversheet required at time of submission. Wed-Sat 10a-6:30p. 32H/week. The... ...inquiries or complaints from consumers, regulatory agencies, or other service providers....RegulatoryFull timeContract workLocal areaShift workAfternoon shift$47.5k
...+ Uncapped Commission (OTE $75-80,000 year one) Upcoming start dates: January 12, 2026 & February 9, 2026 Today our professional services business... ...imbalance exists: Supply Chain Life Sciences Technology Regulatory & Legal Our business is unique in many ways, one of which...RegulatoryWeekly payFull timeJanuary startFlexible hours$100k
...more Role Type: Full-time, permanent Start Date: We are currently recruiting for start dates throughout 2026 and you will be asked to state your... ...economic models or health technology assessment submissions. You will therefore be exposed to a wide variety...Permanent employmentFull timeTemporary workWork from homeFlexible hours$52 - $85 per hour
...studies, maintaining GLP compliance and regulatory standards. Facilitate transparent... ..., data templates, and regulatory submission materials (IND, IB). Maintain and improve... ...: Flexible based on project needs Start Date: June or July 2026 Pay Range: $52 - $85 per hour (...RegulatoryHourly payContract workFor contractorsFlexible hours$1,157 per week
...Contract Duration: 13 Weeks Start Date: 6/8/2026 About the Position TravelNurseSource... ...and coversheet required at time of submission. Wed-Sat 10a-6:30p. 32H/week. The... ...inquiries or complaints from consumers, regulatory agencies, or other service providers....RegulatoryPermanent employmentFull timeContract workTemporary workLocal areaShift workAfternoon shift- Biostatistician II job at Harvard University. Boston, MA. Company Description By working at Harvard... ...has a term appointment of one year from date of hire with the possibility of... ...dental, and vision health insurance coverage starting on day one Retirement plans with university...Worldwide
- ...Laborer II Location: Southwest Corridor Park Start Date:6/08/26 End Date:10/31/26 Work Hours: 40... ...repairs and maintains signs such as regulatory, historic and information signs by... ...Laborer II- Southwest Corridor Park Summer 2026 Location: Massachusetts-Boston-38...RegulatoryFull timeTemporary workPart timeWork experience placementSummer workSeasonal workLive inWork at officeWeekend work
- Vertex Pharmaceuticals Incorporated seeks a Principal Biostatistician to perform advanced statistical analyses for clinical trials and observational... ...teams and contribute to important statistical reports and regulatory interactions. The role requires a PhD or Master's in...Regulatory
£65k - £77k per year
...Kingdom • Salary/rate: £65,000 to £77,000 • Discipline: Regulatory • Job ref: CT2043 • Post Date: 14-04-2026 03:11 PM Cure Talent are delighted to be partnered... ...on regulatory pathways and ensuring high-quality submission content, with particular focus on Module 3...RegulatoryPermanent employment- ...A biotechnology company in Boston is seeking a Regulatory Affairs professional to coordinate and prepare document packages for regulatory submissions. The role involves providing regulatory support, preparing technical documents, and ensuring compliance with FDA regulations...RegulatoryWork at office
- ...AVEO Pharmaceuticals is seeking an Executive Director of Regulatory Operations to lead global submission management and ensure compliance and quality across submissions. The role requires extensive experience in regulatory operations and managing high-performance teams...Regulatory
$246.33k - $304.29k
...Akebia Therapeutics is seeking a Senior Director, Regulatory Affairs in Cambridge, MA to lead regulatory strategy and submissions for innovative therapies addressing chronic kidney disease. This role demands extensive regulatory experience, with leadership responsibilities...RegulatoryFlexible hours- ...Monte Rosa Therapeutics is seeking a Regulatory Operations Manager in Boston, MA. This role demands over 5 years of experience in regulatory operations with proficiency in eCTD submissions and vendor oversight. The candidate will manage regulatory databases, maintain compliance...Regulatory
- ...Monte Rosa Therapeutics, Inc is seeking an experienced regulatory affairs professional in Boston, MA. Responsibilities include coordinating regulatory workflows, compiling submissions to the FDA, and providing ongoing support to project teams. The ideal candidate holds...Regulatory
$177k - $278.08k
...JobRx, Inc. is seeking a Regulatory Affairs professional in Boston, MA to manage regulatory CMC strategy for pharmaceutical products... ...10+ years of experience with a strong focus on leading major submissions and ensuring regulatory compliance. This position offers a hybrid...Regulatory- ...leading pharmaceutical company is looking for a Director of Regulatory Affairs to provide strategic and operational leadership in developing... ...products. The candidate will prepare regulatory submissions, interact with health authorities like the FDA, and ensure compliance...Regulatory
- ...Research (CBAR) is actively recruiting a Biostatistician/Manager of Statistical Training to act... ...PLEASE NOTE: This position has a term end date of November 30, 2027, with strong... ...dental, and vision health insurance coverage starting on day one Retirement plans with university...Remote work
- ...Page Mechanical Group, Inc. is looking for an Executive Director of Regulatory Operations and Submission Management. This strategic role oversees the global regulatory processes ensuring high-quality submissions and compliance across the product lifecycle. The ideal candidate...Regulatory
Do you want to receive more vacancies?
Subscribe and receive similar vacancies to Biostatistician, Regulatory Submissions (2026 Start Date). Be the first to apply!



