NewResearch Tech I Brigham and Women's HospitalResearch Tech IBoston, MA$21–$29.01 / hourWe are seeking bright and highly motivated individual interested in developing skills and experience in biomedical and translational research as a research assistant at the Massachusetts General Hospital Cardiovascular Research Center and Harvard Medical School in the laboratory of Paul B. Research assistants are expected to serve as co-authors for publications during their tenure, with previous members publishing in journals including Science Translational Medicine and American Journal of Respiratory and Critical Care Medicine.
Research Lab Tech I, Hematology Hollenhorst Lab Brigham and Women's HospitalResearch Lab Tech I, Hematology Hollenhorst LabBoston, MA$20.16–$29.01 / hourThe laboratory works closely with the National Center for Functional Glycomics at Beth Israel Deaconess Medical Center and is affiliated with the Broad Institute of Harvard and MIT, the Dana-Farber/Harvard Cancer Center and the Harvard Chemical Biology PhD Program. The framework is comprised of ten competencies (half People-Focused, half Performance-Focused) and are defined by observable and measurable skills and behaviors that contribute to workplace effectiveness and career success.
Director, US Health Economics and Outcomes Research & Real-World Evidence ImCheck Therapeutics SASDirector, US Health Economics and Outcomes Research & Real-World EvidenceCambridge, MA$190,000–$275,000 / yearThe Director, US Health Economics and Outcomes Research (HEOR) & Real World Evidence (RWE) is responsible for identifying real-world and economic evidence needs and developing the real-world, clinical, humanistic, and economic evidence generation plans in collaboration with internal business partners to support the value of our products for US healthcare providers, population-health decision makers, and other external stakeholders for the assigned Therapeutic Area. Drive effective cross-functional collaboration and lead the development of US HEOR evidence generation strategies in alignment with medical and commercial priorities, including strategies supporting products focused on the assigned conditions.
Associate Director, Medical Writing AlkermesAssociate Director, Medical WritingWaltham, MARemote$175,000–$190,000 / yearThe Associate Director is accountable for document development strategy, planning, and execution; leads clinical content development for complex submissions (including content strategy, organization, and resourcing); and partners with Clinical Development, Regulatory Affairs, Biostatistics, and other key functions to ensure cohesive messaging, mitigate risk, and support successful regulatory interactions and filings. In 2024 and 2025, we were certified as a Great Place to Work in the U.S. and named one of Massachusetts' Top Places to Work by the Boston Globe, a Best Place to Work in Greater Cincinnati by the Cincinnati Business Courier and recognized as a Best Place to Work in BioPharma by Fortune Magazine.
Research Leader DMPK, Cambridge, MA Isomorphic Labs LimitedResearch Leader DMPK, Cambridge, MACambridge, MABy harnessing AI's powerful capabilities, we can use it to model complex biological phenomena to help design novel molecules, anticipate how drugs will perform and develop innovative medicines to treat and cure some of the world's most devastating diseases. At Isomorphic Labs, DMPK Leads drive the DMPK strategy of drug discovery projects to deliver high quality clinical candidates whilst using and contributing to the optimisation of state-of-the-art computational and AI ADME models.
Research Leader Toxicology, Cambridge, MA Isomorphic Labs LimitedResearch Leader Toxicology, Cambridge, MACambridge, MAIf you are an experienced, innovative and ambitious scientist looking to play an active part in the AI-driven transformation of the pharmaceutical industry, joining Isomorphic Labs will lift you out of your comfort zone and provide an amazing opportunity for personal growth and development. Since Isomorphic Labs outsource all wet-lab work to external vendors, you will maintain and develop close relationships with the CRO network to: Ensure high quality and timely data generation to support our portfolio projects.
Sr. Applied Research Engineer - OCE - Burlington MA Glaukos CorpSr. Applied Research Engineer - OCE - Burlington MABurlington, MADesign, implement, and experimentally evaluate different corneal imaging modalities and elastography approaches, including comparative performance analysis, sensitivity, repeatability, and clinical relevance, to inform system design and future technology directions. The ideal candidate will bring deep expertise spanning experimental system development, signal processing and algorithm design, and biomechanical modeling, with a strong interest in translating research concepts into robust, validated technologies.
Associate Medical Director Hematology, US OBU Medical Affairs Takeda Pharmaceutical Co LtdAssociate Medical Director Hematology, US OBU Medical AffairsBoston, MA$169,400–$266,200 / yearThe 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.
NewPharmacovigilance and Patient Safety Associate VeristatPharmacovigilance and Patient Safety AssociateMassachusettsFinal salary is ultimately decided upon taking into account a wide range of factors, including but not limited to: skills and experience, licensure and certifications, education, specific location and dynamic market data. They work closely with other departments, sponsors, and investigator sites to ensure that proper plans are in place to appropriately collect and report information on Adverse Events (AEs) and Serious Adverse Events (SAEs).
Administrative Associate - FHC (2026-49951) University of MassachusettsAdministrative Associate - FHC (2026-49951)Worcester, MAAll Academic Accounting & Finance Administrative Professional Administrative Support Advancement Biotechnology Clinical Research Environmental Health & Safety Executive Faculty Healthcare Human Resources Information Technology Interns Library Maintenance and Facilities Management Nursing Office Assistant Other Post Doc Professional Technician I Public Safety Research Residents Retail & Dining Services Staff Assistant Staff Associate Volunteer. All Bedford Boston Brockton Brockton Canton Charlestown Danvers Devens Fall River Fitchburg Holyoke Jamaica Plain Jamaica Plan Lincoln Mattapan North Hampton North Quincy Pocasset Shrewsbury Springfield Taunton Tewksbury Waltham Westborough Westfield Woburn Worcester Wrentham.
Associate Director, Medical Affairs Ipsen SAAssociate Director, Medical AffairsCambridge, MA$180,000–$250,000 / yearKey responsibilities will include supporting the execution of US-based studies, planning and executing advisory boards, reviewing educational grants, and scientific communications including posters, publications, and congresses activities in close partnership with the Publication and Medical Communications teams. The role will also partner closely with the US and Global Medical Information teams to ensure Medical Information Response documents remain accurate and up to date and may include responsibility for the medical review of both nonpromotional and promotional materials.
Senior Consultant - Clinical Documentation Specialist DeloitteSenior Consultant - Clinical Documentation SpecialistBoston, MA$95,600–$188,400 / yearOther skills include the ability to analyze, act and design action plans upon monthly and quarterly reports related to individual providers, facilities, MS-DRGs, APR, PSIs, severity of illness and risk of mortality, capture rates, quality metrics and can effectively prioritize their work activities. Clinical Payments Optimization: Assisting clients by validating that payments for clinical healthcare services comply with regulatory, clinical based evidence and contractual requirements while also determining that payments are appropriate for the type and level of care provided.
Senior Clinical Pharmacologist Regeneron PharmaceuticalsSenior Clinical PharmacologistCambridge, MA$128,600–$210,000 / yearAs a Senior Clinical Pharmacologist this individual is expected to plan, design, implement and analyze in-vivo and in-vitro pharmacokinetic & pharmacodynamic studies working with Clinical Pharmacology, Quantitative Pharmacology, Pharmacometrics/Pharmacodynamics (PK/PD), Toxicology, Bioanalytical, Therapeutic Focus areas and Clinical Development / Regulatory Affairs teams. Performs analyses such as compartmental modeling, PopPK, translational modelling, disease modelling, Pop PK/PD, E-R analyses (or work closely with Research Specialist or Pharmacometrics Stats Programming team) to deliver Pharmacometrics results, interpretation and discussion.
Clinical Diagnostics Account Executive - Great Lakes LGC LtdClinical Diagnostics Account Executive - Great LakesMilford, MAFocused on five key areas - clinical biochemistry and immunoassay, serology, molecular diagnostics, clinical genomics, and reagents - it has around 450 employees across its four FDA-registered and ISO 13485-certified facilities in the USA and Ireland, and an ISO 9001-certified facility in England. Develop deep understanding and knowledge of all products and services along with develop working knowledge of competitor's products and services to differentiate LGC as a top diagnostics and genomics provider.
Research Analyst I Charles River Laboratories International IncResearch Analyst IShrewsbury, MA$25–$26 / hourWhile performing the duties of this job the employee may frequently be required to wear protective clothing (goggles, face shield, surgical mask, cap, gloves, scrubs, boots), work near toxic or caustic chemicals, work with biohazards, and/or work with live animals with risk of exposure to allergens and/or zoonotic diseases. Backed by more than 650 scientists, our comprehensive, integrated portfolio employs the latest technology and platforms to provide chemistry, biology, and pharmacology services that support clients from the earliest stages of hit identification all the way through to IND.
ML Research Engineer Layer HealthML Research EngineerBoston, MassachusettsYou will work closely with our software engineers, research scientists, and product teams to build ML-native enterprise platforms, ensuring scalability, efficiency, and reliability. We are a Boston-based company, and expect engineers to meet regularly in-person in either our NYC or Boston office (engineers from Boston, NYC, or east coast are welcome).
Vice President, AI Research and Real-World Evidence Flagship Pioneering IncVice President, AI Research and Real-World EvidenceCambridge, MA$263,000–$346,500 / yearFlagship has been recognized twice on FORTUNE's "Change the World" list, an annual ranking of companies that have made a positive social and environmental impact through activities that are part of their core business strategies and has been twice named to Fast Company's annual list of the World's Most Innovative Companies. Many of these companies have addressed humanity's most urgent challenges: vaccinating billions of people against COVID-19, curing intractable diseases, improving human health, preempting illness, and feeding the world by improving the resiliency and sustainability of agriculture.
Research Analyst II Charles River Laboratories International IncResearch Analyst IIShrewsbury, MA$27–$29 / hourFrom individual specialty toxicology and IND enabling studies to tailored packages and total laboratory support, our deeply experienced team can design and execute programs that anticipate challenges and avoid roadblocks for a smooth, efficient journey to market. Perform study preparation activities including the preparation and maintenance of study notebooks, generating data collection documentation, identifying supply needs, performing laboratory setup, and developing and implementing Study Specific Procedures (as appropriate).
NewVice President, AI Research and Real-World Evidence Flagship Pioneering, Inc.Vice President, AI Research and Real-World EvidenceCambridge, MA USA$263,000–$346,500 / yearFlagship has been recognized twice on FORTUNE’s “Change the World” list, an annual ranking of companies that have made a positive social and environmental impact through activities that are part of their core business strategies and has been twice named to Fast Company’s annual list of the World’s Most Innovative Companies. Many of these companies have addressed humanity’s most urgent challenges: vaccinating billions of people against COVID-19, curing intractable diseases, improving human health, preempting illness, and feeding the world by improving the resiliency and sustainability of agriculture.
Application Analyst I Mass General BrighamApplication Analyst ISomerville, Massachusetts$62,836.80–$89,762.40 / yearPrincipal Duties and Responsibilities: -Act as part of a team of software application and workflow experts to design, build, configure, and optimize Epic Research functionality and related research workflows.-Analyze current business processes and translate research, operational, and regulatory requirements into application configuration and workflow solutions.-Partner with investigators, study teams, Digital teams, and enterprise research support groups to implement and support research technology solutions.-Document business requirements and translate those requirements into functional specifications, application configuration, and workflow design.-Design, configure, test, implement, and maintain Epic Research functionality, including associated research workflows and integrations with enterprise research systems.-Coordinate with cross-functional stakeholders including IRB, Research Informatics, Privacy, Information Security, Research Contracting, Supply Chain, and other Digital teams to ensure research workflows are effectively integrated across systems.-Develop and execute test plans, perform software quality assurance activities, and validate new functionality prior to implementation.-Provide ongoing production support by troubleshooting application issues, resolving incidents, identifying root causes, and coordinating timely resolution with internal and vendor support teams.-Participate in system upgrades, new feature implementation, workflow optimization, and continuous process improvement initiatives.-Support Epic Research users by providing application expertise, workflow guidance, and consultation on research functionality and best practices.-Run reports, analyze application data, and perform operational tasks necessary to support the ongoing management of the research application environment.-Participate in weekly On-Call rotation to provide production support for supported applications.-Participate in regular team meetings, project planning, and organizational initiatives to improve research technology services.-Review and contribute to training materials, workflow documentation, and end-user education as needed.-Maintain knowledge of Epic Research functionality, regulatory requirements, and emerging technologies impacting clinical research workflows.-Demonstrate