Clinical Research Enrollment Assistant Adams ClinicalClinical Research Enrollment AssistantWatertown, Massachusetts$24–$30 / hourThis role focuses on the hands-on execution of essential administrative and clinical tasks—such as scheduling, preparing visit materials, supporting participant flow, maintaining source documentation, and completing timely data entry—to ensure efficient site operations and high-quality study conduct. The enrollment RA works closely with the enrollment coordinators to provide insights that inform clinical judgment on participant eligibility and study suitability and assists with screening activities and accurate documentation in compliance with ICH-GCP, study protocols, and regulatory requirements.
Clinical Research Nurse (PRN) Adams ClinicalClinical Research Nurse (PRN)Watertown, MassachusettsThis position will also involve general research-related responsibilities like facilitating the informed consent process, administration of screening procedures, data entry, maintenance of regulatory binders, and other nursing functions as required in support of the clinical trial. As a member of our clinical team, you will work under the supervision of our physician principal investigators and clinical nurse manager on the conduct of pharmaceutical-sponsored clinical trials in accordance with FDA regulations and GCP guidelines.
NewClinical Research Coordinator I Adams ClinicalClinical Research Coordinator IBoston, MA$27–$32 / hourSupport investigational product (IP) accountability for assigned studies, including receipt, storage, dispensing, reconciliation, temperature monitoring, and documentation under supervision, ensuring compliance with protocol and site SOPs. Guided by our core values—Scientific Rigor, Operational Excellence, Commitment to Sponsors and Participants, and Authentic Collaboration—we create an environment where meaningful work drives meaningful change.
Clinical Research Director SanofiClinical Research DirectorCambridge, MA$206,250–$343,750 / yearParticipates and contributes to regulatory and safety documents and discussions: Reviews and/or contributes clinical sections of the Investigator Brochure, IND/IMPD filings, DSUR, development risk management plans. 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 Research Coordinator Peregrine TeamClinical Research CoordinatorBoston, MAPeregrine Team is seeking a Clinical Research Coordinator to support clinical trial operations for a leading pharmaceutical organization. Coordinate day-to-day clinical trial activities, including patient scheduling and follow-ups.
Clinical Research Director - Immunology and Inflammation SanofiClinical Research Director - Immunology and InflammationCambridge, MA$206,250–$343,750 / yearThe Clinical Research Director (CRD), Immunology and Inflammation Therapeutic Area, Solid Organ Transplant focus, is responsible for the development, execution and reporting of clinical trials in support of the registration of a product, directly reporting to the Clinical Lead in charge of the clinical strategy. In addition, the CRD is responsible for the development of abbreviated protocol and clinical protocol, participates to the review process for protocols, study reports, labeling, and contributes/supports interactions with regulatory agencies and ethics committees.
Clinical Research Director - Immunology And Inflammation SanofiClinical Research Director - Immunology And InflammationCambridge, MA$206,250–$343,750 / yearThe Clinical Research Director (CRD), Immunology and Inflammation Therapeutic Area, Solid Organ Transplant focus, is responsible for the development, execution and reporting of clinical trials in support of the registration of a product, directly reporting to the Clinical Lead in charge of the clinical strategy. In addition, the CRD is responsible for the development of abbreviated protocol and clinical protocol, participates to the review process for protocols, study reports, labeling, and contributes/supports interactions with regulatory agencies and ethics committees.
Director (Principal Scientist), Clinical Research, Respiratory Merck & Co IncDirector (Principal Scientist), Clinical Research, RespiratoryBoston, MA$255,800–$402,700 / yearThe Clinical Director is responsible for maintaining a strong scientific fund of knowledge by: Maintaining awareness of scientific developments within his/her area of expertise, in terms of new scientific findings, research methodologies. The Clinical Director (Principal Scientist) has primary responsibility for planning and directing clinical research activities involving new or marketed medicines in the Cardiovascular and Respiratory therapeutic area.
Senior Clinical Research Director SanofiSenior Clinical Research DirectorCambridge, MA$236,250–$393,750 / yearCollaborates with other CRDs within the project, ensures leadership, builds consensus, coordinates action plans with stakeholders to resolve project-related study issues, anticipates potential issues (sharing lessons learned) across the project or study teams. Collaborate with other CRDs within the project, ensure leadership, buildsconsensus, coordinate action plans with stakeholders to resolve project-related study issues, anticipate potential issues (sharing lessons learned) across the project or study teams.
Clinical Research Director, Rare Diseases SanofiClinical Research Director, Rare DiseasesCambridge, MA$206,250–$343,750 / yearExperience / Skills: MD or MD/PhD in a relevant scientific discipline, preferably pulmonology, with at least 2 years relevant experience in clinical development within the pharmaceutical industry, academia, or government agencies such as the NIH, FDA, or other equivalent national or international public health and regulatory organization. On Clinical Development, the CRD: Designs the global clinical development strategy (in close cooperation with other members of the team, particularly Regulatory Affairs end Health Economics) and leads the clinical development with regard to ongoing development activities and planned LCM for labelling changes.
Senior Scientist, Clinical Research Merck & Co IncSenior Scientist, Clinical ResearchBoston, MA$117,000–$184,200 / yearCo-authors clinical sections of protocols, clinical investigator brochures, clinical study reports, Worldwide Marketing Application/Common Technical Document (WMA/CTD) subsections, and regulatory agency update and safety reports, as well as clinical development plans, publications, and abstracts. Experience managing Immunology and/or vaccine trials with an ability to think outside of the box, explore novel ways of working and comfortably navigate ambiguity to drive results also a plus.
Clinical Research Director - Rare Diseases SanofiClinical Research Director - Rare DiseasesCambridge, MA$178,500–$257,833.33 / yearExperience / Skills: MD or MD/PhD in a relevant scientific discipline, preferably pulmonology, with at least 2 years relevant experience in clinical development within the pharmaceutical industry, academia, or government agencies such as the NIH, FDA, or other equivalent national or international public health and regulatory organization. On Clinical Development, the CRD: Designs the global clinical development strategy (in close cooperation with other members of the team, particularly Regulatory Affairs end Health Economics) and leads the clinical development with regard to ongoing development activities and planned LCM for labelling changes.
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.
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.
Director, 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.
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.
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.
Director, Clinical Scientist - Ophthalmology EyePoint IncDirector, Clinical Scientist - OphthalmologyCambridge, MA$197,760–$249,947 / yearAssist with all site initiation activities including site initiation visits, investigator meetings, development and implementation of monitoring plans and annotated monitoring visit report templates and completion and submission of all required clinical trial documents prior to site initiation. Actively assist with clinical trial recruitment strategies with evaluation of actual enrollment against assigned targets and working with investigational sites to meet, and whenever feasible, exceed enrollment targets in collaboration with clinical operations.
Breast Imaging Radiologist Lowell General HospitalBreast Imaging RadiologistBoston, MA$440,000–$535,000 / yearThis position involves performing health assessments, conducting diagnostic tests, diagnosing and managing breast-related health conditions, and collaborating closely with a multidisciplinary team of specialists to ensure the highest quality of patient care. Position Title: Breast Imaging Radiologist - Diagnostic Radiology Location: Tufts Medical Center, Boston, MA Department: Department of Radiology Position Type: Full-time Academic Rank: Assistant, Associate, or Full Professor (commensurate with experience).
Clinical Social Worker/LICSW/South Shore Hospital Dana-Farber Cancer Institute IncClinical Social Worker/LICSW/South Shore HospitalSouth Weymouth, MA$90,200–$96,700 / year1 - Provides biopsychosocial assessment and intervention, crisis intervention, coordination of psychosocial services, and consultation, to reduce cancer-related distress and improve quality of life for patients, families, and caregivers across the trajectory of cancer care; this includes those patients seen for screening for high risk of developing cancer and/or a diagnosis of cancer through to end of life and/or survivorship in collaboration with community mental health partners. Responsibilities if Required: Education if Required: License/Registration/Certification Requirements: Licensed Certified Social Worker - Board of Registration of Social Workers (Massachusetts), Licensed Independent Clinical Social Worker - Board of Registration of Social Workers (Massachusetts).