Sr. Director, Clinical Scientist Replimune Group, Inc.Sr. Director, Clinical ScientistWoburn, MA$256,500–$332,000 / yearThe Senior Director, Clinical Development/Clinical Scientist will report to the VP or Executive Director, of the Early Clinical Development team to ensure the successful execution of clinical development programs and deliverables in partnership across the organization, with external vendors, and with external academicians and collaboration partners. The RPx platform is designed to have a unique dual local and systemic activity consisting of direct selective virus-mediated killing of the tumor resulting in the release of tumor derived antigens and altering of the tumor microenvironment to ignite a strong and durable systemic response.
Sr. Director, Clinical Scientist Replimune Group IncSr. Director, Clinical ScientistWoburn, MA$256,500–$332,000 / yearThe Senior Director, Clinical Development/Clinical Scientist will report to the VP or Executive Director, of the Early Clinical Development team to ensure the successful execution of clinical development programs and deliverables in partnership across the organization, with external vendors, and with external academicians and collaboration partners. The RPx platform is designed to have a unique dual local and systemic activity consisting of direct selective virus-mediated killing of the tumor resulting in the release of tumor derived antigens and altering of the tumor microenvironment to ignite a strong and durable systemic response.
Clinical Scientist, Associate Director Candel Therapeutics IncClinical Scientist, Associate DirectorNeedham, MA$181,000–$194,000 / yearCandel Therapeutics is seeking an experienced and intellectually curious Clinical Scientist to support our oncology clinical development programs, with an initial focus on prostate cancer and opportunities to contribute across additional solid tumor programs, including lung and brain cancer studies. Author and contribute to key clinical and regulatory documents including Clinical Study Reports (CSRs), Investigator Brochures (IBs), protocols, informed consent forms (ICFs), DSURs, clinical narratives, and IND/BLA regulatory submissions.
Decision Scientist - Clinical Informatics (Clinical Data Standards) CVS Health CorpDecision Scientist - Clinical Informatics (Clinical Data Standards)MA$64,890–$158,620 / yearA&BC leverages advanced analytics, clinical informatics, and hypothesis-driven approaches to transform data into actionable, customer-centric insights that drive growth, improve health outcomes, and expand access to healthcare across all CVS Health businesses. Collaborate with data engineering teams to inform data pipeline development, ensuring clinical data is ingested, transformed, and stored in ways that support downstream analytics needs.
Clinical Scientist Skyhawk Therapeutics IncClinical ScientistWaltham, MALead or contribute to key clinical and regulatory documents, including clinical development plans, protocols, investigator brochures, informed consent forms, safety management plans, statistical analysis plan input, clinical study reports, IND/CTA submissions, annual reports, and briefing documents. We use our novel SkySTAR platform (Skyhawk Small molecule Therapeutics for Alternative splicing of RNA) to develop drug candidates directed toward targets for some of the world's most intractable diseases including neurological conditions, cancer, and traditionally "undruggable" targets.
Associate Principal Scientist, Clinical Research Merck & Co IncAssociate Principal Scientist, Clinical ResearchBoston, MA$142,400–$224,100 / yearTranslational Medicine (TMed) drives early clinical development of novel therapeutics by partnering with Discovery Sciences and Late-Stage Clinical Research to translate scientific discoveries into human proof-of-concept and advance the most promising candidates through the pipeline to patients. Leads and directs teams through key study planning, development, and execution activities, including program overviews, issue escalation and mitigation, senior management presentations, cross-functional governance meetings, and advisory meeting preparation.
Senior Clinical Scientist (Cambridge, MA) PhilipsSenior Clinical Scientist (Cambridge, MA)Cambridge, MAPartner with cross-functional teams including R&D, Product Management, Systems Engineering, Regulatory Affairs, Quality, and Usability to ensure clinical workflow requirements, procedural considerations, and physician feedback are incorporated into product design and validation activities. Lead and support clinical collaborations with Key Opinion Leaders, research institutions, and healthcare partners, helping to design and execute studies, including usability, phantom, animal, clinical and other evidence-generation activities.
Applied AI Workflow Clinical Scientist PfizerApplied AI Workflow Clinical ScientistCambridge, MA$139,100–$231,900 / yearThe strongest candidate will have the clinical development experience to recognize where work can accelerate - study design, feasibility, trial conduct, clinical data review, and regulatory readiness - and clinic-omics fluency to connect those workflows to biomarker strategy, endpoint development, patient stratification, and high-dimensional data from clinical and translational studies. ROLE SUMMARY: Drives the practical application of large language models (LLMs) and agentic artificial intelligence (AI) across the Inflammation & Immunology (I&I) portfolio by partnering closely with clinical and scientific teams to identify high-value use cases, building reusable workflows, and ensure adoption, rigor, and impact.
Clinical Scientist - Oncology Takeda Pharmaceutical Co LtdClinical Scientist - OncologyBoston, MA$116,000–$182,270 / yearEDUCATION, EXPERIENCE, KNOWLEDGE AND SKILLS: Bachelor's degree and 6 years, master's degree and 4 years, PharmD degree and 2 years, or PhD and 1 year of clinical research and/or clinical development experience within the pharmaceutical industry, CRO health-related consulting company, or biomedical/clinical experience within academia (or a combination of afore mentioned.). Successfully contributes to interactions with regulatory authorities / agencies and key opinion leaders relevant to assigned compound and participate in meetings with representatives of the regulatory organizations and the identification / contact / maintenance of strong Company relationships with key opinion leaders.
Senior Clinical Scientist Whoop IncSenior Clinical ScientistBoston, MA$145,000–$195,000 / yearOperating with minimal oversight, you will translate clinical and product questions into rigorous research approaches, generate and interpret evidence from clinical, wearable, and real-world data, and communicate findings in a way that informs product decisions, regulatory strategy, and clinical evidence generation. Independently author and review clinical study reports, protocols, statistical analysis plans, literature reviews, clinical evidence summaries, regulatory submission sections, manuscripts, abstracts, and internal scientific memos.
Senior Director, Clinical Scientist Verastem IncSenior Director, Clinical ScientistNeedham, MA$260,000–$300,000 / yearSupports scientific communication through literature review and development/review of abstracts, presentations, and manuscripts; maintains current knowledge of oncology, clinical development, and the external regulatory/scientific environment, and develops strong collaborative relationships across Verastem and with external scientific partners. Authors and leads key study and clinical/regulatory documents, including protocols and synopses, informed consent forms, investigator brochures, briefing books, safety updates, clinical study reports, and clinical sections of regulatory submissions and responses.
Director, Clinical Scientist Verastem IncDirector, Clinical ScientistNeedham, MA$200,000–$260,000 / yearSupports scientific communication through literature review and development/review of abstracts, presentations, and manuscripts; maintains current knowledge of oncology, clinical development, and the external regulatory/scientific environment, and develops strong collaborative relationships across Verastem and with external scientific partners. Authors and leads key study and clinical/regulatory documents, including protocols and synopses, informed consent forms, investigator brochures, briefing books, safety updates, clinical study reports, and clinical sections of regulatory submissions and responses.
Director, Clinical Scientist Dyne TherapeuticsDirector, Clinical ScientistWaltham, MACompany Overview: Dyne Therapeutics is focused on delivering functional improvement for people living with genetically driven neuromuscular diseases. We are developing therapeutics that target muscle and the central nervous system (CNS) to address the root cause of disease. The company is advancing clinical programs for Duche...
Clinical Scientist, Neuroimmunology & Specialty Care, PDT Takeda Pharmaceutical Co LtdClinical Scientist, Neuroimmunology & Specialty Care, PDTBoston, MA$116,000–$182,270 / yearThis role will work within the Neuroimmunology and Specialty Care team to support development of clinical assets across the United States, the European Union, and Japan, including protocol concept and protocol development, study start-up and execution, data cleaning, preparation of clinical study reports, and contributions to regulatory filings. Proven experience preparing clinical study protocols, Clinical Study Reports, integrated clinical statistical reports, and clinical sections for regulatory submissions across multiple regions, including Investigational New Drug and New Drug Application documentation.
NewPart-Time Clinical Laboratory Scientist or Medical Laboratory Scientist or Medical Laboratory Technician or CLS ASCP or MLS ASCP or MLT ASCP in Massachusetts K.A. RecruitingPart-Time Clinical Laboratory Scientist or Medical Laboratory Scientist or Medical Laboratory Technician or CLS ASCP or MLS ASCP or MLT ASCP in MassachusettsWhitman, MAYou can also schedule a time to chat here -https://calendly.com/leahkarecruiting/10min. Click apply or email your resume to leah@ka-recruiting.com/call or text 617-746-2751!
NewAssociate Director or Director, Clinical Scientist Kymera TherapeuticsAssociate Director or Director, Clinical ScientistWatertown, MA$160,000–$275,000 / yearHaving advanced the first degrader into the clinic for immunological diseases, Kymera is focused on building an industry-leading pipeline of oral small molecule degraders to provide a new generation of convenient, highly effective therapies for patients with these conditions. Bachelor's or advanced degree (MSc, PharmD, PhD) in Life Sciences or related field and 8+ years in pharmaceutical clinical drug development, with experience in global clinical trials and program execution.
Director, Clinical Scientist Dyne Therapeutics IncDirector, Clinical ScientistWaltham, MA$222,000–$258,000 / yearClinical Data Review, Interpretation & Safety Oversight: Support ongoing patient-level and aggregate clinical data review, including safety, efficacy, biomarker, pharmacodynamic, endpoint, and protocol compliance data, to identify trends, insights, risks, protocol deviations, safety trend review, patient profile review and other potential issues. Strong cross-functional collaboration and influencing skills, with the ability to build alignment across Clinical Development, Clinical Operations, Biostatistics, Data Management, Pharmacovigilance, Regulatory Affairs, Translational Medicine, Medical Affairs, external vendors, and study sites.
Machine Learning Scientist – Clinical Prediction Iambic TherapeuticsMachine Learning Scientist – Clinical PredictionBoston, MassachusettsYou will identify, curate, and evaluate datasets that support prediction of relevant clinical endpoints (patient- and trial-level outcome modeling, safety/toxicity prediction, and PK/PD response modeling) and fine-tune Enchant to deliver critical clinical insights. This includes developing rigorous, leakage-resistant experimental frameworks, optimizing training, orchestrating runs at scale, and working with colleagues across ML and clinical functions to put these models into the hands of scientists making real therapeutic decisions.
Clinical Scientist MBX BiosciencesClinical ScientistBurlington, MAOur pipeline includes canvuparatide (MBX 2109) for the treatment of chronic hypoparathyroidism, currently preparing for Phase 3 development, and a growing obesity portfolio that includes MBX 4291 in Phase 1 development, MBX 5765, a next-generation amycretin prodrug designed for once-monthly-dosing, as well as MBX 6180, a GLP/GIP/GCGR triple agonist prodrug for once monthly dosing; all of which optimize our PEP platform. Leading role in authoring clinical study protocols/amendments and related study documents (including but not limited to drug specific risk language, ICFs, clinical study training materials, pharmacy manual, laboratory manual, etc.) by translating the strategy and approved concept into executable and efficient clinical studies.
Travel Clinical Laboratory Scientist KPG HealthcareTravel Clinical Laboratory ScientistPittsfield, MAKPG Healthcare is a Staffing Firm that provides diverse Supplemental and Permanent Healthcare Staffing solutions to a side range of clients throughout the nation. From our location in the Western U.S., we build relationships nationwide, ensuring our professionals can access the ideal opportunity for their backgrounds, interests and experience.