Associate Director, Payer & Access Marketing- US Rare Tumors OGSIVEO SpringWorks Therapeutics IncAssociate Director, Payer & Access Marketing- US Rare Tumors OGSIVEOBoston, MA$150,700–$226,000 / yearThis role will lead the development of customer-facing value narratives, access-focused strategy, and tactical execution for key market access audiences, including payers, population-based decision-makers, pharmacists, GPOs, and external thought leaders. The role requires strong cross-functional leadership across Commercial, including marketing, sales, market research, market access, and patient services, as well as close partnership with finance, medical, legal, and regulatory.
Director, Global Marketing Alnylam Pharmaceuticals, Inc.Director, Global MarketingCambridge, MAOverview: The Brand Director, Global Marketing Rare is responsible for defining and driving the global brand strategy for OXLUMO and GIVLAARI, ensuring alignment from global vision through local execution. This role leads cross-functional collaboration to deliver impactful, insight-driven strategies and tactics that maximize patient impact, stakeholder engagement and commercial performance.
Senior Director, Commercialization Technology Architect Vertex Pharmaceuticals, IncSenior Director, Commercialization Technology ArchitectBoston, MA$228,000–$342,000 / yearWe seek talent who bring an external perspective, demonstrate curiosity and sound judgment, and thoughtfully adopt new capabilities that improve decision-making, drive innovation, increase efficiency, and help deliver better outcomes for patients. At Vertex, our Total Rewards offerings also include inclusive market-leading benefits to meet our employees wherever they are in their career, financial, family and wellbeing journey while providing flexibility and resources to support their growth and aspirations.
Senior Director, Head Of PV Science Alnylam Pharmaceuticals, Inc.Senior Director, Head Of PV ScienceCambridge, MAIn partnership with Head of Medical Safety and Risk Management (MSRM), the Senior Director will provide strategic leadership in development and management of safety profiles at all stages of the lifecycle for all Alnylam products, and will have accountability on Alnylam safety aggregate reports for submission to regulatory authorities, including, among others, Periodic Safety Update Reports, Developmental Safety Update Reports, and Risk Management Plans. Work closely with the Head of MSRM and safety leads analyzing MSRM team's needs and potential process improvements in all functions, including routine and ad-hoc signaling activities, clinical trial initiations, regulatory interactions, and aggregate reports production.
Director, Cybersecurity Massachusetts Medical SocietyDirector, CybersecurityWalthamFull timeUnder the auspices of NEJM Group, the MMS extends our mission globally by advancing medical knowledge from research to patient care through the New England Journal of Medicine , NEJM Evidence , NEJM AI , NEJM Catalyst, NEJM Clinician, and through our accredited and comprehensive continuing medical education programs. A leadership voice in health care, the MMS contributes physician and patient perspectives to influence health-related legislation at the state and federal levels, works in support of public health, provides expert advice on physician practice management, and addresses issues of physician well-being.
Associate Director Field Operations Alnylam Pharmaceuticals IncAssociate Director Field OperationsCambridge, MA$174,300–$235,700 / yearThis role partners closely with field leadership and cross-functional stakeholders to ensure field teams are equipped with the right metrics, tools, processes, insights, and governance to execute against business priorities. The Associate Director, Field Force Effectiveness is responsible for driving the effectiveness, execution, and operational excellence of customer-facing field teams across Commercial and Medical Affairs.
Associate Director, HEOR & RWE Les Laboratoires Servier SASAssociate Director, HEOR & RWEBoston, MA$184,000–$218,000 / yearDeep expertise in innovative RWE methodologies required for pipeline assets, including the design of external/synthetic control arms to contextualize single-arm clinical trials and the characterization of unmet medical needs in rare oncology indications. Evidence Generation and Impact Measurement: Oversee the end-to-end delivery of RWE studies (e.g., database analysis, chart reviews, prospective registries) to characterize unmet needs and disease burden in niche solid tumor indications.
Associate Director, Regulatory Project Management Centessa Pharmaceuticals PlcAssociate 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.
NewDirector, Heor - Orexin Franchise Centessa Pharmaceuticals PlcDirector, Heor - Orexin FranchiseBoston, MA$180,000–$260,000 / yearReporting to the Executive Director, HEOR, the, you will partner extensively with Medical Affairs, Clinical Development, Market Access, Commercial, Legal, Regulatory, and external research partners to translate strategic objectives into actionable, well-governed research plans throughout the product lifecycle - from early pipeline evidence generation and launch readiness through post-launch value demonstration. Lead and manage HEOR studies, including retrospective and prospective observational studies, database analyses (claims, EHR, registries), and innovative designs such as external control arms to contextualize single-arm trial data.
NewSales Director (Future Opportunity) Sirtex Medical LtdSales Director (Future Opportunity)Boston, MAThis position supports Sirtex in achieving its commercial objectives through effective sales leadership, talent development, territory and account management, budget oversight, and cross-functional partnership. The Sales Director will work closely with the VP of Sales and other functional leaders to ensure the Sales organization has the leadership, resources, and support necessary to execute against established business objectives.
Director, External Quality Control & Stability Centessa Pharmaceuticals PlcDirector, External Quality Control & StabilityBoston, MA$150,000–$210,000 / 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. The Director, External Quality Control & Stability will provide leadership and oversight for analytical testing, stability programs, specification management, and quality control activities supporting clinical and commercial development.
Associate Director/Director, Medical Operations Scholar Rock Holding CorpAssociate Director/Director, Medical OperationsCambridge, MA$175,000–$255,000 / yearThis role will be a key partner within Medical Affairs and partner with cross-functional leaders including Commercial, Patient Advocacy, Clinical Development, and Market Access to act as a central point of coordination, ensuring seamless communication and effective collaboration. Scholar Rock is a late-stage global biopharmaceutical company focused on developing and commercializing apitegromab for children and adults with spinal muscular atrophy (SMA) and other rare, severe, and debilitating neuromuscular diseases.
NewSenior Director, Medical Affairs - Cardiology Iterative HealthSenior Director, Medical Affairs - CardiologyCambridge, MA$210,000–$265,000 / yearWe built a leading performance-driven network of 100+ sites across the US, Europe, India, and Australia, conducting research directly in the communities where care is delivered across gastrointestinal, hepatology, obesity, and cardiology. By combining deep clinical trial expertise with cutting-edge AI, we connect sponsors' scientific ambitions with high-performing research teams that expedite and expand access to novel therapeutics for patients in need.
Director/Sr. Director, Corporate Controller Frontier MedicinesDirector/Sr. Director, Corporate ControllerBoston, MA$200,000–$290,000 / yearOwn the clinical and R&D accrual process end to end, including building and maintaining accrual workbooks for new programs and trials from CRO and CMO contracts, enrollment and site activation data, and vendor spend, so that estimates are supportable and stand up to audit scrutiny. This is a hands on role for someone who enjoys making the accounting engine work: shortening the close, improving the quality of support, building controls that fit how the business operates, clarifying ownership, and developing a strong team.
New(Associate) Director, Clinical Science Centessa Pharmaceuticals, LLC(Associate) Director, Clinical ScienceBoston, MA$140,000–$210,000 / yearReporting to the Executive Director, Clinical Development, this individual will lead authorship of key clinical and regulatory documents, drive ongoing clinical data review and interpretation, contribute to dose-escalation and development strategy decisions, and provide scientific leadership across internal governance and cross-functional forums. Centessa is seeking an (Associate) Director, Clinical Science to provide scientific and clinical leadership for the design, execution, and interpretation of early-stage (Phase 1/2) clinical trials for our Orexin-targeted programs in neurodegeneration and neuropsychiatric indications.
Clinical Scientist, Associate Director Candel TherapeuticsClinical 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.
Senior Director, Regulatory CMC Centessa Pharmaceuticals, LLCSenior 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.
Assistant Program Director - LICSW LMHC LMFT - Community Behavioral Health Center (CBHC) Riverside Community CareAssistant Program Director - LICSW LMHC LMFT - Community Behavioral Health Center (CBHC)Norwood, MAMost of our jobs come with great benefits – including healthcare, numerous professional development opportunities, and generous time off - all in a respectful and inclusive environment, perhaps why Riverside was named a Boston Globe Top Workplace and a best-in-state employer by Forbes. Maintains clinical leadership and direction in providing program services in an appropriate and time effective manner, including the integration of medical health and behavioral health, commensurate with CBHC mission, regulations, and quality measures.
Associate Director, Clinical Data Management Beeline MedicinesAssociate Director, Clinical Data ManagementBoston, Massachusetts$181,000–$235,000 / yearThe Associate Director, Clinical Data Management Leads clinical data management activities across one or more clinical programs, ensuring the timely delivery of high-quality, audit-ready clinical trial data in support of regulatory submissions and clinical development timelines. Led by an established executive team and backed by world-class life science investors, each day Beeline Medicines is determined to bring the scientific rigor and operational excellence to get to what matters for patients – realizing a world where people with immune-mediated diseases can live life fully.
Director Business Development Syneos Health IncDirector Business DevelopmentBoston, MATogether we share insights, use the latest technologies and apply advanced business practices to speed our customers' delivery of important therapies to patients. Selecting us as an employer secures a career in which you're guaranteed to: Collaborate with passionate problem solvers Partner with the most diverse team of experts in the industry.