Research Scientist - HSPH Dana-Farber Cancer Institute IncResearch Scientist - HSPHBOSTON, MA$145,000–$162,000 / yearThe Department of Data Science at the Dana-Farber Cancer Institute offers an exceptional collaborative environment with experts in a wide range of areas, including clinical trials, cancer genetics, immunology, epigenetics, machine learning, statistical software development, Bayesian methods, and alignment algorithms. Conducts research as an independent investigator or plays a leadership role in research projects, for example, as a senior analyst in one or more research projects, presenting results and preparing publications; collaborating with external researchers or supervising research staff.
Statistical Programmer Rhythm PharmaceuticalsStatistical ProgrammerBoston, MA$110,000–$165,000 / yearThe successful candidate will be responsible for delivering high-quality, compliant analysis datasets, tables, listings, and figures; contributing to study-level and integrated submission deliverables; and partnering closely with Biostatistics, Data Management, Clinical Development, Medical Writing, Regulatory, and external vendors. Lead or support statistical programming activities for assigned clinical studies, including development, validation, and quality control of analysis datasets, tables, listings, and figures for study reports, regulatory submissions, and internal decision-making.
Principal Data Strategist, Real World Evidence (RWE) Boston Scientific CorpPrincipal Data Strategist, Real World Evidence (RWE)Marlborough, MAThis 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.
Associate Director, Statistical Programming Dyne Therapeutics IncAssociate Director, Statistical ProgrammingWaltham, MA$175,000–$204,000 / yearIn collaboration with cross-functional stakeholders, this role provides technical consultation to study teams and supports alignment of statistical programming resources and capabilities to meet organizational priorities. Primary Responsibilities Include: Lead and oversee statistical programming activities across multiple clinical trials and studies, ensuring high-quality deliverables, operational consistency, and adherence to timelines.
Onnela Lab Postdoctoral Research Fellow Position in Network Science / Causal Inference Harvard UniversityOnnela Lab Postdoctoral Research Fellow Position in Network Science / Causal InferenceCambridge, MAThis position involves developing new theory and methods at the intersection of causal inference and network science, building software, and potentially collaborating on applied health sciences projects. D. in biostatistics, applied mathematics, computer science, or a related quantitative field for a one-year Postdoctoral Research Fellow position.
NewExecutive Medical Director, Clinical Development, Hematology AlexionExecutive Medical Director, Clinical Development, HematologyBoston, MassachusettsThe Executive Medical Director (EMD) role is generally assigned to be responsible for overseeing 2 or more programs, providing oversight/guidance/mentoring to the Medical Directors and Clinical Development Scientists on the teams, serving on cross-asset strategic teams (e.g., disease strategy team) and providing input to strategic decisions at the TA Strategy Team and Global Medicine Team meetings. 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.
NewSenior Medical Director Clinical Development Neurology AlexionSenior Medical Director Clinical Development NeurologyBoston, Massachusetts$288,059.20–$432,088.80 / yearServe 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 ).
Translational Project Lead Statistician SanofiTranslational Project Lead StatisticianWaltham, MA$122.25–$176.58 / hourAs Translational Project Lead Statistician within Vaccines Global Biostatistics Sciences (GBS), you are the ultimate scientific owner of all statistical translational deliverables for your assigned project(s), bringing your quantitative passion to project translational sub-team which consists of translational strategic expert, biomarker lab scientist, immunology lead and research experts. Serve as statistical subject matter expert to collaborate with cross functional stakeholders in research, immunology, biomarker labs, clinical development, and global project management in the extended project team.
Associate Director, Statistical Programming Dyne TherapeuticsAssociate Director, Statistical ProgrammingWaltham, MA$175,000–$204,000 / yearIn collaboration with cross-functional stakeholders, this role provides technical consultation to study teams and supports alignment of statistical programming resources and capabilities to meet organizational priorities. The company is advancing clinical programs for Duchenne muscular dystrophy (DMD) and myotonic dystrophy type 1 (DM1) as well as a preclinical programs for facioscapulohumeral muscular dystrophy (FSHD) and Pompe disease.
Data & Analytics Lead Integrated Resources, IncData & Analytics LeadBoston, MassachusettsContractorEducation & Experience• Bachelor's degree, preferably in a scientific discipline such as Statistics, Mathematics, Economics, Computer Science, IT, Biology, Social Science, etc.• 8+ years relevant work experience with a focus on data management and/or data analysis• Deep understanding of drug development and biopharmaceutical industry required• Strong project management skills, and ability to effectively lead and collaborate with various business functions project management certified desirable• High attention to detail including proven ability to manage multiple, competing priorities• Experience overseeing outsourced clinical trials work• Demonstrated ability to establish effective business relationships with external stakeholders, including implementing process change at a vendor• Deep knowledge of clinical data management and statistical programming outsourcing with full-service, global CROs and FSPs• Demonstrated ability to influence without authority• Excellent written and oral communication skillsAdditional InformationJay KaushikClinical RecruiterIntegrated Resources, Inc Liaises directly with internal customers (CDS functions, GCO, Biostatistics, and Regulatory Affairs) and external customers (Full Service and Functional Service Provider Data Leads and Project Management personnel, all other external Partners (affiliates, etc.).• Serves as Subject Matter Expert for data, reporting, and analysis process definition, improvement, and innovation as needed.•
statistical programmer(SAS Programmer) Integrated Resources, Incstatistical programmer(SAS Programmer)Cambridge, MassachusettsContractorSupport for Inspection Readiness and Regulatory InspectionsRequired:7+ years relevant work experience in Data Management, Biostatistics or Statistical Programming.7+ years relevant work experience in GCP Quality with significant interaction with Data Management, Biostatistics or Statistical Programming. Associate, Biometrics QualityLocation: Cambridge, MADuration: 12+ months (possibility of extension)Roles & Responsibilities:The Biometrics Quality Team provides leadership and support for the Global Biometrics department, which consists of Data Management, Biostatistics and Statistical Programming.
Biostatistical Data Programmer CorronaBiostatistical Data ProgrammerWaltham, MassachusettsSummary of Position: The Biostatistical Data Programmer will work under the guidance of a Biostatistician/Data Scientist in database management and data sciences to support the development, programming and maintenance of data, tools and processes for the Corrona data lifecycle and business integrity. Education/Experience: Required: • Bachelor’s Degree with a least 3 years’ experience or Master’s Degree plus 1 year experience in Biostatistics, Statistics, Mathematics, Applied Mathematics or Computer science with a concentration in Statistics or Mathematics.
Clinical Scientist TScan TherapeuticsClinical ScientistWaltham, MA$145,000–$155,000 / yearThe Clinical Scientist will be responsible for leading ongoing clinical data review activities, developing data review strategies, identifying and resolving data issues, and ensuring high-quality clinical datasets are available to support safety reviews, regulatory submissions, and clinical decision-making. This unique role sits at the intersection of Clinical Development, Clinical Operations, Data Management, and Biostatistics serving as a critical driver of data quality, data integrity, and clinical insight generation.
Research Technology Specialist - Human Nutrition Research Center on Aging Tufts UniversityResearch Technology Specialist - Human Nutrition Research Center on AgingBoston, MABasic Requirements: Knowledge and experience typically acquired by: Bachelor's Degree in biomedical engineering, computer science, data science, electrical engineering, bioinformatics, biostatistics, computational biology, applied mathematics, or a related quantitative or technical field. This position will contribute to data-rich research projects involving human studies, observational cohorts, lifestyle interventions, biomarker analytics, wearable and sensor-derived data, and high-dimensional omics datasets.
Executive Medical Director, Clinical Development, Hematology, Nephrology, & Transplant, Cell Therapy AstraZeneca PlcExecutive Medical Director, Clinical Development, Hematology, Nephrology, & Transplant, Cell TherapyBoston, MAThe Executive Medical Director (EMD) role is generally assigned to be responsible for overseeing 2 or more programs, providing oversight/guidance/mentoring to the Medical Directors and Clinical Development Scientists on the teams, serving on cross-asset strategic teams (e.g., disease strategy team) and providing input to strategic decisions at the TA Strategy Team and Global Medicine Team meetings. 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.
Senior Medical Director Clinical Development Neurology Alexion Pharmaceuticals IncSenior Medical Director Clinical Development NeurologyBoston, MA$280,895.20–$421,342.80 / yearYou 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 ).
Executive Medical Director, Clinical Development, Hematology, Nephrology, & Transplant, Cell Therapy Alexion Pharmaceuticals IncExecutive Medical Director, Clinical Development, Hematology, Nephrology, & Transplant, Cell TherapyBoston, MAThe Executive Medical Director (EMD) role is generally assigned to be responsible for overseeing 2 or more programs, providing oversight/guidance/mentoring to the Medical Directors and Clinical Development Scientists on the teams, serving on cross-asset strategic teams (e.g., disease strategy team) and providing input to strategic decisions at the TA Strategy Team and Global Medicine Team meetings. 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.
Associate Principal, Indirect Treatment Comparison (ITC), Evidence Synthesis IQVIA Holdings IncAssociate Principal, Indirect Treatment Comparison (ITC), Evidence SynthesisBoston, MARemote$125,800–$350,300 / yearAssociate Principals are project leaders who are responsible for implementing rigorous evidence synthesis research, overseeing the work of junior staff, and proactively managing the project timeline. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time).
Head of AI Clinical Excellence Pfizer IncHead of AI Clinical ExcellenceCambridge, MA$176,600–$294,300 / yearYou will partner closely with the Oncology Clinical Development, Clinical Operations, Biostatistics, Data Science, Medical Affairs, Regulatory Affairs, and Digital organizations to identify, develop, and scale AI-driven capabilities that improve trial design, data review, study execution, operational efficiency, decision-making, and regulatory readiness. 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.