Payer Stars/Quality Clinical Consultant, Senior Manager PwCPayer Stars/Quality Clinical Consultant, Senior ManagerBoston, MA$124,000–$280,000 / yearAs a Payer STARS/Quality Clinical Consultant, Senior Manager, you will engage with clients in the health services sector, providing strategic guidance and operational consulting to enhance their clinical quality and performance metrics. PwC does not intend to hire experienced or entry level job seekers who will need, now or in the future, PwC sponsorship through the H-1B lottery, except as set forth within the following policy: https://pwc.to/H-1B-Lottery-Policy .
Payer STARS/Quality Clinical Consultant, Senior Manager PricewaterhouseCoopers LLPPayer STARS/Quality Clinical Consultant, Senior ManagerBoston, MA$124,000–$280,000 / yearAs a Payer STARS/Quality Clinical Consultant, Senior Manager, you will engage with clients in the health services sector, providing strategic guidance and operational consulting to enhance their clinical quality and performance metrics. PwC does not intend to hire experienced or entry level job seekers who will need, now or in the future, PwC sponsorship through the H-1B lottery, except as set forth within the following policy: https://pwc.to/H-1B-Lottery-Policy .
Postdoctoral Research Fellow Beth Israel Lahey HealthPostdoctoral Research FellowBoston, Massachusetts0-1 year of postdoctoral research experience in academic or industrial lab setting, and/or teaching assistantship in a university setting, and/or residency, and/or clinical duties beyond that of the qualifying doctoral degree. Problem Solving: Ability to address problems that are varied, requiring analysis or interpretation of the situation using direct observation, knowledge and skills based on general precedents.
Statistical Project Leader SanofiStatistical Project LeaderCambridge, MA$148,500–$214,500 / yearOur Evidence Generation and Decision Science (EGDS) group at Sanofi unites Biostatistics, Clinical Statistical Modeling, and Real-World Evidence to revolutionize data-driven decision making through cutting-edge quantitative science and deliver unparalleled integrated evidence that drives innovation and scientific breakthroughs. Basic Qualifications: PhD/MS in statistics or related discipline with at least 5 years of pharmaceutical experience in clinical development, including experience with Biotech, pharma, Clinical Research Organizations (CROs), health authorities and academic clinical research centers.
NewDirector, Training Strategy & Process Enablement ModernaTXDirector, Training Strategy & Process EnablementCambridge, MassachusettsWe are proud to have been recognized as a Science Magazine Top Biopharma Employer, a Fast Company Best Workplace for Innovators, and a Great Place to Work in the U.S. If you want to make a difference and join a team that is changing the future of medicine, we invite you to visit modernatx.com/careers to learn more about our current opportunities. The Director will establish scalable frameworks for role-based learning, change management, training effectiveness, and knowledge management while driving innovation in learning methodologies, digital learning technologies, and organizational capability development.
Senior Medical Science Liaison Northeast Rapport Therapeutics IncSenior Medical Science Liaison NortheastBoston, MA$190,000–$210,000 / yearBy fostering trusted scientific relationships, generating meaningful insights, and supporting evidence development, the MSL helps shape Medical Affairs strategy while contributing to a team culture where people support one another, learn together, and celebrate shared success. Build, maintain, and serve as a primary scientific contact for peer-to-peer relationships with scientific leaders, investigators, healthcare professionals, and academic centers within the assigned geography.
Associate Director, Quantitative Systems Pharmacology GSK plcAssociate Director, Quantitative Systems PharmacologyWaltham, MA$151,500–$252,500 / yearAs an Associate Director of Quantitative Systems Pharmacology (QSP) Expert, you will develop and apply QSP models to guide clinical study designs and mechanistic interpretation of study results in support of development of treatments and combination of treatments for a variety of diseases and therapeutic areas. This role requires a highly motivated individual to develop and apply QSP models to guide clinical study designs and mechanistic interpretation of study results in support of development of treatments and combination of treatments for a variety of diseases and therapeutic areas.
Head, Global Oncology Strategic Market Research & Advanced Analytics Innovation 3310 Takeda Pharmaceuticals U.Head, Global Oncology Strategic Market Research & Advanced Analytics InnovationBoston, MassachusettsLead the transformation of insights and analytics by anticipating industry and competitive signals, setting a clear vision aligned to enterprise priorities, and modernizing traditional data approaches (including GenAI), while identifying, piloting, and scaling innovative analytics and emerging technologies in close partnership with enterprise leaders and Global Capabilities Centers—to enable foresight driven strategy, decision making, and immediate business impact. This role will serve as a critical thought partner to Global Oncology leadership, shaping objective, forward-looking external market understanding that acts as a catalyst behind strategy, portfolio decisions, launch, and lifecycle execution across pipeline and inline assets.
Senior Machine Learning Research Engineer (Deep Learning, Sensor Intelligence Group) WhoopSenior Machine Learning Research Engineer (Deep Learning, Sensor Intelligence Group)Boston, MA$150,000–$215,000 / yearYou will tackle the complex challenge of extracting reliable insights from noisy sensor data and deploying robust algorithms on constrained edge and cloud environments, ultimately delivering meaningful and personalized metrics to millions of members. At WHOOP, we view total compensation as the combination of base salary, equity, and benefits, with equity serving as a key differentiator that aligns our employees with the long-term success of the company and allows every member of our corporate team to own part of WHOOP and share in the company's long-term growth and success.
Research Senior Scientist 3316 Takeda Development Center AmericasResearch Senior ScientistBoston, MassachusettsPOSITION DESCRIPTION : Takeda Development Center Americas, Inc. is seeking a Research Senior Scientist in Cambridge, MA with the following duties: serve as the DMPK representative on projects to support gastroenterology, autoimmune and oncology Drug Discovery Units (DDUs) for developing novel drug therapy by providing molecular and cellular analysis support; Serve as the DMPK representative on projects to support gastroenterology, autoimmune and oncology Drug Discovery Units (DDUs) for developing novel drug therapy by providing molecular and cellular analysis support; support early drug development and translational research by providing scientific support with a focus on cellular and molecular quantification using cutting-edge technology, such as flow cytometry, ddPCR, Nanostring nCounter, and other assay platforms; communicate with internal stakeholders regarding the project needs, progress updates, and DMPK deliverables; perform innovative assay development, trouble-shoot bioanalytical assay related issues, and actively identify/adopt/develop novel technologies for capability building and to meet the ever-changing needs of projects together with key stakeholders in DMPK, different DDUs, and other Quantitative Preclinical and Translational Sciences (QPTS) groups; design, validate and implement new methodologies and processes (including in silico approaches) that contribute to the research goals of the group/department; summarize and present the experimental results in the cross-functional project teams and DMPK meetings; provide scientific monitoring and guidance to external resources (CRO) for the method transfer, development, trouble shooting, qualification, validation and report to support non-/pre-clinical development programs. Prior experience must include: lead hypothesis-driven investigative research including in vitro, ex vivo and in vivo studies to drive novel therapeutic development including animal handling and biological sample handling; design, optimize, and implement molecular, cellular, bioanalytical, and biomarker assays including ELISA, PCR, neutralization assay, proliferation, flow cytometry and ELISPOT to assess transgenes, recombinant proteins, cytokines, antibodies, and immunogenicity for efficacy studies; apply advanced computational and statistical approaches to analyze and interpret large, complex datasets to support decisionmaking; analyze nucleotide and peptide sequences using bioinformatics or in silico tools to create and evaluate synthetic primers, plasmids, and other synthetic genes and peptides to support therapeutics development.
Research Affairs Specialist - School of Dental Medicine Tufts UniversityResearch Affairs Specialist - School of Dental MedicineBoston, MassachusettsThe main function of the role is performing regulatory approval functions which includes working with study teams to develop study protocols, consent forms, and supporting documentations, facilitating IRB approval, study start-up activities, and monitoring study progress. Work with study teams to obtain start up approval for non-human subject research projects and survey studies, including review of study protocols, creation of recruitment supporting documentation, ensuring all study team members have CITI/GCP training.
NewDirector, Global Real-World Evidence & Health Outcomes Research Scientist- Hepatology GSK plcDirector, Global Real-World Evidence & Health Outcomes Research Scientist- HepatologyWaltham, MA$185,250–$308,750 / yearThe role of Director, Global Real-World Evidence & Health Outcomes Research Scientist is critical to achieving this ambition by supporting asset teams to ensure that each medicine GSK brings to market is supported by scientifically credible, high quality, evidence that drives competitiveness and strong evidence-based product positioning, value propositions and value-based pricing. We need to better understand how our customers define value and to effectively collaborate with them to ensure we are generating value evidence data that includes real world evidence and cost effectiveness analysis that is impactful for payers, health systems, providers, and patients.
AI/ML Research Engineer Manifold Bio IncAI/ML Research EngineerBoston, MAYou will be expected to take ownership of engineering challenges in our ML pipeline, from data processing and model training to deployment and monitoring, while collaborating closely with our research team to translate cutting-edge ideas into robust, scalable systems. Our in vivo-centric discovery platform produces millions of experimentally validated protein designs per campaign, creating the datasets that make our models possible and our approach uniquely powerful.
NewAssociate Medical Director Hematology, US OBU Medical Affairs 3310 Takeda Pharmaceuticals U.Associate Medical Director Hematology, US OBU Medical AffairsBoston, MassachusettsThe actual base salary offered may depend on a variety of factors, including the qualifications of the individual applicant for the position, years of relevant experience, specific and unique skills, level of education attained, certifications or other professional licenses held, and the location in which the applicant lives and/or from which they will be performing the job. This role involves monitoring regulatory developments, ensuring compliance, and preparing regulatory documents to support Takeda's mission of delivering transformative therapies to patients.
Sr Clinical Consultant Point32Health, Inc.Sr Clinical ConsultantCanton, MA$109,730–$164,595 / yearWe value the rich mix of backgrounds, perspectives, and experiences of all of our colleagues, which helps us to provide service with empathy and better understand and meet the needs of the communities where we serve, live, and work. Scam Alert: Point32Health has recently become aware of job posting scams where unauthorized individuals posing as Point32Health recruiters have placed job advertisements and reached out to potential candidates.
Clinical Supply Chain Project Leader SanofiClinical Supply Chain Project LeaderCambridge, MA$105–$151.67 / hourThe CSC-PL will also ensure clear, concise, consistent, and timely communication with stakeholders and act as a change agent through the leadership of global initiatives targeting process improvement and engaging all partners throughout the clinical supply chain. But progress doesn't happen without people - people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen.
Clinical Utilization Management Pharmacist Point32Health, Inc.Clinical Utilization Management PharmacistCanton, MA$110,680.66–$166,020.98 / yearPerforms case reviews in automated prior authorization (Auto PA) tools and guides the case through the entire process to either approval or denial to ensure all coverage determinations and notices are consistent with applicable regulatory and accreditation requirements and turnaround times. Communicate with UM staff and providers when issues arise regarding policy interpretation, potential access availability or other quality assurance issues to ensure that members receive coverage determinations within timelines developed by all accrediting and regulatory guidelines.
CMC Synthetics Clinical Manufacturing Leader SanofiCMC Synthetics Clinical Manufacturing LeaderCambridge, MA$148.50–$214.50 / hourThe Projects and External Technologies team, part of the CMC Synthetics organization within Sanofi R&D, is responsible for the delivery of clinical drug substance and drug product batches in full compliance with project requirements, Sanofi policies and GMP regulation, leveraging internal and external manufacturing capabilities. Under the direction of Projects and External Technologies department head, the primary responsibility of this role is to coordinate and oversee internal and external GMP clinical manufacturing activities, with the aim of supplying clinical trials with drug substance and drug product.
Vice President, Clinical Development Beam Therapeutics IncVice President, Clinical DevelopmentCambridge, MA$310,000–$400,000 / yearThe VP of Clinical Development will oversee implementation and maintenance of all metabolic internal clinical development programs and will also have the strategic view and excellence in execution to continue to grow the strength and scope of the internal pipeline, in addition to participating in potential business development opportunities, including additional acquisitions. 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.
Executive Director, Clinical Science and Innovation Lead, Early Oncology Development AstraZeneca PlcExecutive Director, Clinical Science and Innovation Lead, Early Oncology DevelopmentWaltham, MA$304,856.80–$457,285.20 / yearDepartmental Leadership: Contribute to the Early Oncology Clinical Science & Clinical Development leadership teams on strategy, objectives, resourcing, and issue resolution; oversee departmental capacity management and talent deployment across programs. Cross-functional collaboration: Co-lead collaboration with the Research Scientists and Translational Scientists to shape pre-CDID and FiH strategies; provide clinical input on data generation and interpretation to enable high-quality, decision-ready development plans.