Director, Therapeutic Area Strategy, CRM Novartis AGDirector, Therapeutic Area Strategy, CRMCambridge, MA$176,400–$327,600 / yearIn-depth TA knowledge (or track record to acquire required TA expertise effectively and rapidly) in CRM.Highly agile having the capacity to support a number of strategic DAs within a TA and multiple programs internal and externalSubstantial experience evaluating new product opportunities (through M&A, BD&L and internal re-search programs).At least 5-7 years of Industry pharma and/or medical devices Experience in Research & Development and/or commercial functions with experience conducting, commissioning, analyzing primary researchExperience of strategy development and asset shaping early in lifecycle (any functional perspective)Recent (post 2015) local US in-market experience; local US experience includes working within the US market with the local US customers, US health care systems / systemsBenefits & Rewards The salary for this position is expected to range between $176,400 and $327,600 per year. Supports development and delivery of TA-specific strategic external insights to support identification of growth opportunities, emerging competitive challenges and support creation of a third-party view around key strategic levers, and commissions targeted primary research.
Director, Regulatory Writing Entrada Therapeutics IncDirector, Regulatory WritingBoston, MARemote$220,000–$249,711 / yearReporting to the Senior Vice President, Regulatory Affairs, the successful candidate will support the development of strong internal processes, be the key liaison with external writing providers, serve as a lead author and document specialist, and support documentation planning and submission activities. We expect multiple clinical data readouts as we advance several DMD programs across the U.K., EU, and U.S. By year-end 2026, we anticipate four clinical-stage programs in our DMD franchise (ENTR-601-44, ENTR-601-45, ENTR-601-50, and ENTR-601-51).
Director, Market Research & Insights Collegium Pharmaceutical IncDirector, Market Research & InsightsBoston, MA$218,000–$262,000 / yearKnowledge of emerging AI applications in pharmaceutical market research, including large language models (LLMs), machine learning, and natural language processing (NLP), with the ability to evaluate, integrate, and optimize AI-driven methodologies to improve research efficiency and business insights. The Director, Market Research & Insights will be responsible for leading the strategy, development, execution, and communication of market research and insight-generation capabilities that enable customer-centered, evidence-based decision making across the commercial organization.
Associate Director, Heor AlkermesAssociate Director, HeorWaltham, MARemote$179,000–$205,000 / yearWorking closely with cross-functional partners, the successful candidate will support a broad range of HEOR activities, including generation of real-world evidence (RWE), health economic models and assessments, payer value communications, scientific presentations and publications, and other strategic support throughout the product lifecycle. 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.
Senior Director, DMPK Project Leader Centessa Pharmaceuticals, a wholly owned subsidiary of Eli Lilly and CompanySenior Director, DMPK Project LeaderBoston, MA$200,000–$215,000 / yearCentessa Pharmaceuticals, a wholly owned subsidiary of Eli Lilly and Company, is a clinical-stage company developing orexin receptor 2 (OX2R) agonists as a new class of medicines for the treatment of narcolepsy and potentially other sleep-wake disorders. Centessa's OX2R agonist portfolio includes additional clinical and preclinical-stage assets with potential utility across a broader range of neurological, neurodegenerative, and neuropsychiatric conditions.
Associate Director, Clinical Supply Chain Centessa Pharmaceuticals, a wholly owned subsidiary of Eli Lilly and CompanyAssociate Director, Clinical Supply ChainBoston, MA$130,000–$180,000 / yearCentessa Pharmaceuticals, a wholly owned subsidiary of Eli Lilly and Company, is a clinical-stage company developing orexin receptor 2 (OX2R) agonists as a new class of medicines for the treatment of narcolepsy and potentially other sleep-wake disorders. Reporting to the Senior Director, Clinical Supply Chain this individual will develop strong collaborative relationships with several internal departments as well as third-party procurement, packaging, and distribution providers to align objectives and implement decisions which ensure clinical supply.
Director, Therapeutic Area Strategy, Neuroscience Novartis AGDirector, Therapeutic Area Strategy, NeuroscienceCambridge, MA$176,400–$327,600 / yearHighly agile having the capacity to support a number of strategic DAs within a TA and multiple programs internal and externalSubstantial experience evaluating new product opportunities (through M&A, BD&L and internal re-search programs).At least 5+ years of Industry pharma and/or medical devices Experience in Research & Development and/or commercial functions with experience conducting, commissioning, analyzing primary researchExperience of strategy development and asset shaping early in lifecycleRecent (post 2015) local US in-market experience; local US experience includes working within the US market with the local US customers, US health care systems / systemsBenefits & RewardsThe salary for this position is expected to range between $176,400 and $327,600 per year. The Novartis Strategy & Growth, Therapeutic Area Strategy team for Neuroscience is seeking a new Therapeutic Area Strategy Director who will support the creation and update of a holistic TA strategy; provide early-phase commercial insights to project teams; guide TA-specific internal pipeline development and external licensing / acquisitions opportunities; and support integrated enterprise alignment across Biomedical Research (BR), Development, Strategy & Growth (S&G), and the Commercial US and International units.
NewSenior Director, Regulatory CMC Centessa Pharmaceuticals, a wholly owned subsidiary of Eli Lilly and CompanySenior Director, Regulatory CMCBoston, MA$175,000–$260,000 / yearCentessa Pharmaceuticals, a wholly owned subsidiary of Eli Lilly and Company, is a clinical-stage company developing orexin receptor 2 (OX2R) agonists as a new class of medicines for the treatment of narcolepsy and potentially other sleep-wake disorders. Reporting to the Executive Director, Regulatory CMC, you will lead Regulatory CMC initiatives, develop and execute global CMC regulatory strategies, partner with internal and external stakeholders, and oversee CMC regulatory submissions across our portfolio.
NewSenior Director, Global Regulatory Strategy Centessa Pharmaceuticals, a wholly owned subsidiary of Eli Lilly and CompanySenior Director, Global Regulatory StrategyBoston, MA$225,000–$275,000 / yearCentessa Pharmaceuticals, a wholly owned subsidiary of Eli Lilly and Company, is a clinical-stage company developing orexin receptor 2 (OX2R) agonists as a new class of medicines for the treatment of narcolepsy and potentially other sleep-wake disorders. As the Senior Director, Global Regulatory Strategy you will report to the VP, Regulatory and Medical Writing and serve as a key member within our regulatory team, providing strategic and operational regulatory leadership across global development programs.
NewAssociate Director, Regulatory Project Management Centessa Pharmaceuticals, a wholly owned subsidiary of Eli Lilly and CompanyAssociate Director, Regulatory Project ManagementBoston, MA$140,000–$200,000 / yearServing as the central hub for regulatory projects, the Regulatory Project Manager (RPM) is accountable for regulatory project timelines, ensuring effective planning, tracking, execution, and delivery of submissions to health authorities worldwide. Centessa Pharmaceuticals, a wholly owned subsidiary of Eli Lilly and Company, is a clinical-stage company developing orexin receptor 2 (OX2R) agonists as a new class of medicines for the treatment of narcolepsy and potentially other sleep-wake disorders.
Director, R&D Legal, Americas Novartis AGDirector, R&D Legal, AmericasCambridge, MA$194,600–$361,400 / yearEssential requirements:Juris Doctor (J.D.) or equivalent law degree and admission to practice law in at least one U.S. jurisdiction.8+ years' post bar admission legal experience in life sciences industry (preferably biotechnology or pharmaceutical) or a top-tier law firm representing pharmaceutical clients and advising senior leaders on complex legal, regulatory, and business risks. Sign up to our talent community to stay connected and learn about suitable career opportunities as soon as they come up: https://talentnetwork.novartis.com/networkBenefits and Rewards: Read our handbook to learn about all the ways we'll help you thrive personally and professionally: https://www.novartis.com/careers/benefits-rewards .
Associate Director, HCP Marketing, Lumryz (Ih) AlkermesAssociate Director, HCP Marketing, Lumryz (Ih)Waltham, MARemote$165,000–$190,000 / yearIn 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. We have a portfolio of proprietary commercial products for the treatment of alcohol dependence, opioid dependence, schizophrenia, bipolar I disorder and narcolepsy, and a pipeline of clinical and preclinical candidates in development for various psychiatric and neurological disorders.
NewAssociate Director - Antibody Discovery Programs Alloy Therapeutics IncAssociate Director - Antibody Discovery ProgramsWaltham, MA$150,000–$200,000 / yearCommunicate: Communicate effectively with key stakeholders externally and internally, fostering productive interactions both upward and downward, and across teams at different sites. This role will report directly to the site head Antibody-Powered Division Waltham, MA, with autonomy owning various stakeholders, projects, and tasks in a dynamic start-up environment while keeping up the pace of Alloy.
NewDirector, Corporate Communications Keurig Dr Pepper IncDirector, Corporate CommunicationsBurlington, MA$155,500–$200,000 / yearJob Overview: As the Coffee Operating Unit of Keurig Dr Pepper prepares to become a global coffee company, the Senior Director, US External Communications & Corporate Brand will play a critical role in shaping and protecting the company's corporate reputation and narrative in the United States. The successful candidate will partner closely with Global Corporate Affairs, Investor Relations, Legal, Sustainability, and senior leadership to navigate complex business moments, strengthen stakeholder engagement, and position the company as a trusted global coffee leader.
Associate Director, Regulatory Advertising And Promotion AlkermesAssociate Director, Regulatory Advertising And PromotionWaltham, MA$185,000–$197,000 / yearIn 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. We have a portfolio of proprietary commercial products for the treatment of alcohol dependence, opioid dependence, schizophrenia, bipolar I disorder and narcolepsy, and a pipeline of clinical and preclinical candidates in development for various psychiatric and neurological disorders.
NewDirector, Global Patient Advocacy Lead AlexionDirector, Global Patient Advocacy LeadBoston, MassachusettsJoining Alexion means working where every day is driven by the needs of people living with rare and devastating diseases, where diverse perspectives are welcomed, different thinking is encouraged, kindness sits alongside ambition, and teams are empowered to innovate at pace while staying closely connected to the communities they serve. The Director, Patient Advocacy will be responsible for driving, building and enhancing strategic alliances with both disease-specific advocacy organizations and those that span across disease area umbrella groups, as well as other rare/ultra-rare disease-oriented organizations in response to patient needs to drive Alexion AstraZeneca Rare Disease global patient advocacy strategic goals. .
NewDirector of Rehabilitation (DOR) – Skilled Nursing Facilities (SNFs) – Multiple Massachusetts Locations Relient HealthDirector of Rehabilitation (DOR) – Skilled Nursing Facilities (SNFs) – Multiple Massachusetts LocationsBoston, MassachusettsLicensed Physical Therapists (PTs), Occupational Therapists (OTs), Speech-Language Pathologists (SLPs), Physical Therapist Assistants (PTAs), or Certified Occupational Therapy Assistants (COTAs). Relient Health is seeking experienced Directors of Rehabilitation (DORs) for full-time, in-person leadership opportunities within established rehabilitation departments across Massachusetts.
NewDirector, Product Marketing Pmlg (Marketing Team) SEMrush Holdings Inc.Director, Product Marketing Pmlg (Marketing Team)Boston, MA$224,848–$341,769 / yearIn this role, you will lead a team of Product Marketing Managers who will follow your example to ensure we champion our customer needs according to our ICPs, craft compelling narratives that are rooted in Unique Selling Propositions (USPs), and partner across teams to deliver world-class marketing campaigns that drive new user acquisition and expansion MRR, as well as overall customer lifetime value. This position will require a deep understanding of sales-led go-to-market (GTM) strategy, laser focus on experimentation, pricing and packaging, product lifecycles, and the discipline to make data-driven decisions, and, most importantly, always putting the customer first.
NewDirector, Supplier Quality, Inspection & Audit Centessa Pharmaceuticals, a wholly owned subsidiary of Eli Lilly and CompanyDirector, Supplier Quality, Inspection & AuditBoston, MA$150,000–$210,000 / yearThe Director, Supplier Quality, Inspection & Audit role will provide strategic leadership and tactical support for supplier quality management, GxP supplier audit programs, inspection readiness, and supplier quality oversight across the portfolio. Centessa Pharmaceuticals, a wholly owned subsidiary of Eli Lilly and Company, is a clinical-stage company developing orexin receptor 2 (OX2R) agonists as a new class of medicines for the treatment of narcolepsy and potentially other sleep-wake disorders.
Director, Regulatory Advertising and Promotion Genetix Biotherapeutics IncDirector, Regulatory Advertising and PromotionSomerville, MA$185,000–$285,000 / yearThe Director serves as a key regulatory partner to Medical Affairs, Commercial, Marketing, and Legal, and plays a central role in promotional material review in a highly regulated environment, for cell and gene therapy products. Actual base salary pay will be based on several factors, including but not limited to experience, skills, relevant education/qualifications, external market, internal equity, and other job-related factors permitted by law.