Medical Director - PACE East Boston Neighborhood Health Center CorporationMedical Director - PACERevere, MassachusettsPartner with NeighborHealth’s CMO and senior leadership to align clinical strategies, ensuring the PACE program’s localized care model meets broader enterprise objectives. Whether you're a nurse or physician providing direct care, a manager leading dedicated teams, or part of the essential support staff who keep our operations running smoothly — every role at NeighborHealth is vital.
US Neurology And Immunology Asset/Indication Lead SanofiUS Neurology And Immunology Asset/Indication LeadCambridge, MA$148,500–$214,500 / yearDesign and execute Health Economic and Outcomes Research (HEOR) research in the forms of economic modeling, database analysis, observational research, systematic literature review, evidence synthesis, post hoc analysis of clinical trials, AMCP dossier development and other types of HEOR studies/deliverables to support value demonstration and differentiation in US market. The HEVA department gathers a wealth of expertise including experts in Health Economic and Outcomes Research (HEOR), Indirect Treatment Comparison & Network Meta Analysis (ITC/NMA), Modelling, Health Technology Assessment (HTA), epidemiology, biostatistics, and generation of real word evidence (RWE).
US Heva Neurology Asset/Indication Lead SanofiUS Heva Neurology Asset/Indication LeadCambridge, MA$178,500–$257,833.33 / yearThrough a focused and rapidly expanding portfolio of innovative therapies - addressing a range of neurological conditions where patients continue to face significant unmet need- Sanofi aims to address critical gaps in care and deliver meaningful, potentially transformative treatment options for patients living with neurological disorders. The HEVA department gathers a wealth of expertise including experts in Health Economic and Outcomes Research (HEOR), Indirect Treatment Comparison & Network Meta-Analysis (ITC/NMA), Modelling, Health Technology Assessment (HTA), Evidence Synthesis, Epidemiology, Biostatistics, and generation of Real World Evidence (RWE).
Post Market Surveillance (PMS) Specialist Katalyst Healthcares & Life SciencesPost Market Surveillance (PMS) SpecialistCambridge, MAServes as a liaison between Medical Affairs, Clinical Affairs, Research & Development, Services, and Complaint Handling to ensure Post Market Surveillance (PMS) and Risk Management (RM) processes are executed end-to-end (E2E). Minimum of 4-5 years' experience in Post Market Surveillance within FDA/EU-MDR regulated Medical Device environments with a focus on post-market surveillance plans/reports and post market risk assessment.
Senior AI/ML Engineer Sarepta Therapeutics IncSenior AI/ML EngineerCambridge, MA$152,400–$190,500 / yearCross-Functional Collaboration: Partner with stakeholders from R&D, Clinical Operations, Regulatory Affairs, and other departments to understand needs and translate them into data science questions and production solutions; provide guidance and enablement to colleagues. Data and Infrastructure: Work closely with IT, Enterprise Data Systems (EDS), and data engineering teams to ensure the availability, quality, and governed use of data required for AI/ML initiatives.
Global Asthma HCP Marketing Associate - VIE Contract SanofiGlobal Asthma HCP Marketing Associate - VIE ContractCambridge, MAAs Global Asthma HCP Marketing Associate VIE within our Alliance Immunology team, you'll make an impact on patients' and their families' lives with Dupixent that truly can transform lives of patients with Severe Asthma but also patients that suffer from COPD, Atopic Dermatitis, Chronic Rhinosinusitis with Nasal Polyposis, Prurigo Nodularis and Eosinophilic Esophagitis. Soft and technical skills: Demonstrated ability to communicate innovative science in an easy to understand and compelling way (internally, externally), leveraging excellent communication and presentation skills.
Senior Director, Supplier & External Manufacturing Quality Integra LifeSciences Holdings Corp.Senior Director, Supplier & External Manufacturing QualityMansfield, MA$192,050–$263,350 / yearThis role ensures that external manufacturing partners, critical suppliers, and service providers consistently meet regulatory, quality, and business requirements while enabling operational excellence, scalability, and risk‑based decision making. The Senior Director, Supplier & External Manufacturing Quality is responsible for providing global strategic leadership and governance for supplier quality management and contract manufacturing quality across the enterprise.
Medical Director, Pulmonary SanofiMedical Director, PulmonaryCambridge, MA$206,250–$343,750 / yearMain responsibilities: Develop strategy and tactics for an integrated Medical Plan (Medical Education, Medical Communications and Publications, Health Outcomes, Safety, and Clinical Research including Phase IIIB-IV and Investigator Sponsored Trials) and annual budget for assigned the respective therapeutic area products. Ensure strategic and cross-functional alignment across the organization and any joint ventures to achieve the medical mission of supporting safe and appropriate use of the respective therapeutic area products, cultivating a culture of teamwork and collaboration to ensure the delivery of key priorities.
NewGlobal Development Medical Director, Cell Therapy Oncology AstraZeneca PlcGlobal Development Medical Director, Cell Therapy OncologyCambridge, MA$249,827.20–$374,740.80 / yearThe Global Development Medical Director is an important part of the Clinical Project Team (CPT), and Global Study Team (GST) working collaboratively and cross functionally (in a matrix environment) with other CPT, GST and GPT members, Site Management & Monitoring (SMM), field-based liaisons, and site personnel. Emerging communication & presentation skills including the ability to clearly communicate scientific concepts/data to leadership committees (e.g LSPC, DRC, PRC) or external groups (e.g Investigator Meetings, IDMCs, Conferences.
Kidney Field Training Associate Director Vertex PharmaceuticalsKidney Field Training Associate DirectorBoston, Massachusetts$157,000–$235,600 / yearThe Associate Director, Kidney Training & Development is a strategic leadership role responsible for designing and leading capability-building initiatives that support the success of the Kidney business at Vertex. Design, implement, and manage comprehensive training programs for the Kidney BU Field teams focused on unbranded education, product launch readiness, product launch and continuous upskilling.
Associate OrchestraAssociateBoston, WashingtonSome of our current and former clients include American Service Project, Bezos Earth Fund, Citizens for Responsible Energy Solutions, Centerline Liberties, Inseparable, National Council for Mental Wellbeing, Project Right Side, Trust for Public Land, and Voices for Healthy Kids. We enlist experts, leverage relationships, and build coalitions to address some of the most pressing political and societal challenges of our day, including conservation and clean energy, early care and family strengthening, contraceptive care and access, election modernization, and LGBTQ freedom.
Clinical Project Manager Integrated Resources, IncClinical Project ManagerLexington, MassachusettsContractorJob Position: Clinical Project Manager Location: Lexington, MA Duration: 6 Months+ (Temp to Perm) Summary: The Clinical Project Manager is responsible for independently managing a small number of studies of basic to moderate complexity or defined activities in more complex, multicenter studies (e.g., managing niche vendors). Our methods include applying domain expertise in specific industry segments, utilizing a highly-skilled workforce, leveraging a proven global delivery model, implementing structured and scalable quality processes and methodologies and yet, staying cost-effective.
Principal Specialist - Regulatory Affairs & Compliance Gorton'sPrincipal Specialist - Regulatory Affairs & ComplianceGloucester, MassachusettsMonitor and evaluate emerging regulatory trends, enforcement actions, recalls, and global food safety risks to proactively manage regulatory risks and ensure company strategies remain aligned with current and future compliance requirements. - Provide technical expertise to support Gorton’s businesses in all areas related to ingredients, labeling and claims, legal, governmental and regulatory issues, including FDA registration requirements.
Senior Supplier Quality Engineer Job Details | Olympus Corporation Of The Americas OlympusSenior Supplier Quality Engineer Job Details | Olympus Corporation Of The AmericasWestborough, MAThe Senior Supplier Quality Engineer is responsible for the product-related supplier quality within a defined material segment and / or site including part approval, SCAR handling, development project support, sustaining engineering support including non-conformance handling, and incoming inspection planning and SCN handling. Accountable for and manages Supplier Change Notification (SCN) process for sourced materials by closely and proactively working with Procurement and other cross-functional areas as necessary for timely assessment, documentation and disposition of supplier requested changes.
Principal System Engineer Full SpectrumPrincipal System EngineerWestborough, MAThe Opportunity: Strategic Leadership & Client Impact: In this high-visibility role, you serve as the primary technical interface for our clients, driving Software Systems Engineering for mission-critical medical device projects: Lead & Delegate: Manage project execution by aligning client needs with team tasks and deliverables. Safety Risk Analysis: Lead planning for complex software-driven medical devices, perform top-down hazard and harm assessment working with Full Spectrum clients’ clinical tam or medical director, performing bottom-up failure analysis (FMEA) and identifying potential risk to safety.
Director, Medical Information Xenon PharmaceuticalsDirector, Medical InformationNeedham, MassachusettsThis role drives functional priorities for, and execution of medical inquiry management, scientific response content development, contact center operations, and digital medical information capabilities to support Medical Affairs, Clinical Development, and Commercial launch readiness. Our Total Rewards program includes base salary, target bonus, and stock options, as well as a full range of benefits including medical, dental, vision, short-& long-term disability, accidental death & dismemberment, and life insurance programs, Employee Assistance Program, travel insurance, and retirement savings programs with company matching contributions.
Director, Corporate Communications Xenon PharmaceuticalsDirector, Corporate CommunicationsNeedham, MassachusettsUnder the leadership of the Senior Vice President of Corporate Affairs, this role will also work with the CEO, CFO, CMO, CCO and other senior leaders to execute the Corporate and Investor Relations strategy, and effectively develop messaging and communications for our scientific, clinical, and financial progress to various stakeholder groups including investors, media and investigators. Lead development of corporate messaging and materials, including press releases, Q&As, corporate presentations, executive talking points, social media content, etc., in collaboration with Corporate Affairs, Brand Communications, the CFO, CEO, Medical Affairs, Clinical Development, Commercial, Legal, Regulatory, and other parts of the organization.
NewExecutive Medical Director, Oncology Clinical Sciences 3316 Takeda Development Center AmericasExecutive Medical Director, Oncology Clinical SciencesBoston, 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. OBJECTIVES: The Executive Director (ED) is responsible for ensuring ongoing review and agreement of the therapy area strategy and associated documents formulated by the Oncology Therapeutic Area Unit (OTAU) prior to their review and approval by appropriate governance committees.
Data & Analytics Lead Integrated Resources, IncData & Analytics LeadCambridge, MassachusettsFull timeThe Data and Analytics Lead manages the end to end clinical data flow (data acquisition from Case Report Form (CRF) to Clinical Study Reporting (CSR) of Clinical Data) and ensures timely project execution; recognized as an operational specialist in data flow and study execution by all functions. Liaises directly with internal customers (CDS functions, GCO, Biostatistics, and Regulatory Affairs) and external customers (Full Service and Functional Service Provider Data Leads and Project Management personnel, all other external Partners (affiliates, etc.).
Clinical Data and Analytics Lead Integrated Resources, IncClinical Data and Analytics LeadCambridge, MassachusettsFull time5+ years relevant work experience with a focus on data management • Deep understanding of drug development and biopharmaceutical industry required • Strong project management skills, and ability to effectively lead and collaborate with various business functions • High attention to detail including proven ability to manage multiple competing priorities • Experience overseeing outsourced clinical trials work performed by vendors • Demonstrated ability to establish effective business relationships with external stakeholders, including implementing process change at vendor • Deep knowledge of clinical data management with full-service global CROs and FSPs • Demonstrated ability to influence without authority • Excellent written and oral communication skill. Liaises directly with internal customers (Medical functions, Statistical Programming, Clinical Operations, Biostatistics, Regulatory Affairs) and external customers (Full Service and Functional Service Provider Data Leads and Project Management personnel).