Senior Director, Clinical Quality Assurance Alkermes PlcSenior Director, Clinical Quality AssuranceWaltham, MAA member of the Alkermes Quality leadership team responsible for overall Quality culture and continuous improvement of Alkermes QMS and compliance, and leads the Alkermes strategy and GXP compliance on all matters concerning Quality in the areas of; Good Laboratory Practices (GLP), Good Clinical Practices (GCPs), and Good Pharmacovigilance Practices pre and post market (GVPs). Oversee the development, implementation, and continuous improvement of clinical quality systems, harmonized GCP/GVP/GLP Policies, processes, SOPs, and governance structures collaborating closely with Clinical Department, related functions and external partners to comply with global requirements.
Sr Global Product Manager, MCT Clinical Systems PhilipsSr Global Product Manager, MCT Clinical SystemsCambridge, MA$130,000–$209,000 / yearAs our Senior Product Manager within Philips Ambulatory & Monitoring Diagnostics (AM&D) Service Solutions team, you will collaborate in defining the Mobile Cardiac Telemetry (MCT) clinical systems product strategy for that aligns to the AM&D portfolio vision and global market alignment. The actual base pay offered may vary within the posted ranges depending on multiple factors including job-related knowledge/skills, experience, business needs, geographical location, and internal equity.
Sr Global Product Manager, Clinical Systems PhilipsSr Global Product Manager, Clinical SystemsCambridge, MA$130,000–$209,000 / yearAs our Senior Product Manager within Philips Ambulatory & Monitoring Diagnostics (AM&D) Service Solutions team, you will collaborate in defining the clinical systems product strategy that aligns to the AM&D portfolio vision and global market alignment. The actual base pay offered may vary within the posted ranges depending on multiple factors including job-related knowledge/skills, experience, business needs, geographical location, and internal equity.
Senior Program Coordinator Integrated Resources, IncSenior Program CoordinatorBoston, MAThe Senior Program Coordinator works independently while managing priorities, resolving complex issues, maintaining confidentiality, and ensuring accuracy of academic records. The Senior Program Coordinator will support multiple areas within the Office of the University Registrar, including enrollment, registration, graduation, records integrity, academic scheduling, and reporting.
Senior Machine Learning Engineer TechStarsGroupSenior Machine Learning EngineerBoston, MassachusettsYou'll have the opportunity to work with the latest NLP technologies and help to invent, implement, test, and release new technologies that push the state of the art in extracting sophisticated semantics from biomedical text sources, including anonymized EMRs (electronic medical records). As a senior ML engineer you'll assume a leading role in an agile team of ML and software engineering practitioners who collaborate closely with our product and clinical scientist teams.
Senior Director, Pharmacovigilance (PV) Process Lead Takeda Pharmaceutical Co LtdSenior Director, Pharmacovigilance (PV) Process LeadCambridge, MA$212,000–$333,190 / yearCultivates trusted, enterprise-wide relationships with key stakeholders across Takeda (e.g., Regulatory, Quality Assurance, Global Development Operations, Clinical Science, Medical Affairs, Commercial, Local Operating Companies, DD&T), demonstrating executive presence and strategic influence while serving as the central orchestrator to ensure strong PV oversight and performance, identifying risks, driving issue resolution, and promoting alignment and decision-making among cross-functional stakeholders. Champions technology and AI-enabled capabilities to drive continuous process improvement, operational excellence, and efficiency by streamlining the E2E processes, defining clear roles and responsibilities, and ensuring that they are in-line with regulatory requirements to maintain inspection readiness at all time.
Senior Manager GCP Quality Regeneron PharmaceuticalsSenior Manager GCP QualityUxbridge, MA$134,400–$219,200 / yearWe are seeking a Senior Manager, GCP Quality Management - Global Development to join our Global Development Quality team, supporting our global clinical development organisation in a hybrid work model. In this role, you will lead risk-based quality management across clinical trials while collaborating with study teams, clinical functions, contract research organisations, and quality colleagues.
Senior Toxicologist Regeneron PharmaceuticalsSenior ToxicologistCambridge, Massachusetts$128,600–$210,000 / yearToxicologist will demonstrate a thorough understanding of GLP regulations and FDA/EMEA/ICH nonclinical safety guidelines to independently lead the design, conduct, interpretation, and reporting of regulatory toxicology and/or exploratory pharmacology/toxicology studies in rodent and non-rodent safety models. The Senior Toxicologist utilizes their scientific expertise and regulatory experience to lead nonclinical development programs with guidance from her/his direct supervisor working effectively within cross-functional project teams.
Sr. Scientist, Therapeutics & Translational Bioinformatics Moderna IncSr. Scientist, Therapeutics & Translational BioinformaticsCambridge, MA$145,900–$234,200 / yearWe 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. This person will apply expertise in computational biology, immunology, machine learning/AI, and advanced statistical methods to identify therapeutic targets, biological mechanisms, biomarkers, response signatures, and patient-level factors that inform program strategy.
Senior Pathologist PathAISenior PathologistBoston, MassachusettsYou will serve as a Pathology lead on Biopharma and other projects to recommend scoring approaches, help select network or KOL Pathologists, develop and provide training to clinical trial study readers, participate in manual and digital scoring of Pathology cases in various indications, and conduct internal assay validations. You will provide Pathology subject matter expert guidance on new potential products, work with multidisciplinary teams to help develop new DP/AI models, assist in model deployments, review the outputs and statistics from the PathAI machine learning algorithms, and provide insights on the overall improvement of the output.
NewSenior Director, Medical Affairs Editas Medicine IncSenior Director, Medical AffairsCambridge, MADecoding The Role: The primary focus of this role is to lead medical and scientific strategic planning and operational execution of core medical affairs activities from early-clinical phase through lifecycle management for our lead in vivo development candidate, EDIT-401, a potential best-in-class, one-time therapy designed to significantly reduce LDL cholesterol levels. This role will build Medical Affairs capabilities while providing scientific leadership and strategic direction across cross-functional teams and strong engagement with external stakeholders.
Sr. Director, Head, Quantitative Systems Pharmacology Moderna IncSr. Director, Head, Quantitative Systems PharmacologyCambridge, MA$196,700–$353,400 / yearIn addition to leading QSP strategy and capabilities, this role is expected to serve directly as the CQP representative within key program teams, driving model-informed drug development strategy and enabling portfolio decisions in close partnership with cross-functional leaders. This leader will define and execute the vision for how mechanistic modeling, systems biology, and model-informed drug development (MIDD) approaches are applied across discovery, preclinical, and clinical stages to accelerate early development decisions, strengthen translational understanding, and optimize dose, schedule and patient selection strategies.
Senior Director, AIRx Discovery Biology Lead Takeda Pharmaceutical Co LtdSenior Director, AIRx Discovery Biology LeadBoston, MA$212,000–$333,190 / yearThe AIRx Discovery Biology Lead combines deep scientific expertise with the agility to thrive in an externalized, AI-powered operating model - leveraging biological depth and pragmatism to direct and integrate biology at speed, while role modeling new ways of working in Discovery Automation & Robotics (DAR) group. Responsibilities include directing CRO partners with precision and accountability to generate high-quality, interpretable data that feeds into AI-powered DMTA cycles, and connecting experimental biology to translational strategy and clinical outcomes.
Sr. Regulatory Affairs Specialist Glaukos CorpSr. Regulatory Affairs SpecialistBurlington, MAOur constant pursuit of game-changing technologies that disrupt legacy treatment paradigms is encapsulated in the Glaukos mantra "We'll Go First," which articulates our willingness to take chances, our determination to forge new ground, and our commitment to continuous improvement in all that we do. Founded in 1998, Glaukos Corporation is an ophthalmic pharmaceutical and medical technology company focused on developing and commercializing novel therapies for the treatment of glaucoma, corneal disorders, and retinal diseases.
Senior Product Manager, Healthcare WhoopSenior Product Manager, HealthcareBoston, MassachusettsWorking cross-functionally with engineering, design, data science, clinical, regulatory, and commercial teams, you will deliver innovative, evidence-based experiences that transform complex health data into actionable insights, helping members better understand and improve their health. 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.
Rheumatology (Senior) Medical Director - Medical Affairs Swedish Orphan Biovitrum ABRheumatology (Senior) Medical Director - Medical AffairsWaltham, MA$224,000–$290,000 / yearDevelop and foster strong collaborative relationships with internal partners, including Regulatory Affairs, Clinical Operations, Market Access, Medical Information, Pharmacovigilance, Sales, and Marketing, and provide medical insight and product- and disease-state expertise to meet business objectives. Develop a US evidence generation strategy to address stakeholder (HCPs, payers, and patients) needs (including product differentiation, health outcomes), collaborating with HEOR and global partners.
Senior Manager, Scientific Communications, Global Medical Affairs Oncology 3310 Takeda Pharmaceuticals U.Senior Manager, Scientific Communications, Global Medical Affairs OncologyBoston, MassachusettsThe role leads cross-functional publication planning teams and collaborates closely with Medical Affairs, Clinical Development, Outcomes Research, and regional and global stakeholders to deliver high-impact scientific publications and medical communication materials, including manuscripts, congress presentations, scientific slide decks, NCCN and pathway submissions, field medical tools, training materials, digital content, animations, websites, and other scientific resources. The Senior Manager, Scientific Communications is a highly visible strategic leadership role within Takeda Oncology’s Global Medical Affairs Oncology organization, supporting the company's mission to aspire to cure cancer by driving the scientific publications and communications strategy for assigned hematology oncology assets.
Senior Director, Outcomes, Value & Access Kymera TherapeuticsSenior Director, Outcomes, Value & AccessWatertown, MA$235,000–$330,000 / 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. The ideal candidate is an experienced HEOR leader with deep immunology expertise (dermatology and/or respiratory strongly preferred), a proven track record preparing for and supporting launches, and significant experience engaging national and regional payer stakeholders.
Senior Manager, Veeva Regulatory & Data Scholar RockSenior Manager, Veeva Regulatory & DataCambridge, MAReporting to the Senior Director, Commercial & Data, the Senior Manager partners closely with business stakeholders, Quality and Validation, Cybersecurity, Data & Analytics, Infrastructure & Cloud, and external technology partners to translate business priorities into scalable, secure, compliant, and sustainable technology solutions. The Senior Manager leads solution delivery from requirements and design through implementation and ongoing support, maintains sufficient hands-on expertise to independently assess, configure, and troubleshoot complex Veeva solutions, and ensures internal and external delivery teams provide reliable, high-quality services.
Senior Director, Discovery & Translational De Solid Biosciences IncSenior Director, Discovery & Translational DeMA$260,000–$305,000 / yearSolid Biosciences is a precision genetic medicine company focused on advancing a portfolio of gene therapy candidates targeting rare neuromuscular and cardiac diseases, including Duchenne muscular dystrophy (Duchenne), Friedreich's ataxia (FA), catecholaminergic polymorphic ventricular tachycardia (CPVT), TNNT2-mediated dilated cardiomyopathy, BAG3-mediated dilated cardiomyopathy, and additional fatal, genetic cardiac diseases. The successful candidate will lead a team responsible for multiple pipeline programs, including Friedreich's ataxia, CPVT, emerging genetic cardiomyopathy programs, additional new pipeline opportunities, and clinical assay oversight across advancing programs.