Pioneering Medicines: Director, In Vivo Pharmacology - Metabolic Disease Flagship Pioneering IncPioneering Medicines: Director, In Vivo Pharmacology - Metabolic DiseaseCambridge, MA$172,000–$236,500 / yearFlagship has been recognized twice on FORTUNE's "Change the World" list, an annual ranking of companies that have made a positive social and environmental impact through activities that are part of their core business strategies, and has been named four times to Fast Company's annual list of the World's Most Innovative Companies. Harnessing the drug development expertise of its team together with the power of Flagship''s multiple scientific platforms, Pioneering Medicines explores and identifies new product concepts which are then advanced jointly with Flagship's bioplatform companies.
Director RA CMC AbbVie IncDirector RA CMCWaltham, MAPrepares and manages regulatory submissions, including new IND/CTA applications and amendments, new marketing authorization submissions, renewals, annual reports, supplements and variations, and/or leads a global RA CMC team who develops strategies for development and marketed products. Represents RA CMC on teams such as the product development, Global Regulatory Product Teams and Operations Product Teams, for assigned projects; negotiates with and influences team members to maximize chances for first pass approval of regulatory submissions.
NewAssociate Director, Global Program Management, Neuroscience TAU Takeda Pharmaceutical Co LtdAssociate Director, Global Program Management, Neuroscience TAUCambridge, MA$154,400–$242,550 / yearResponsibilities include providing strategic direction and translating the cross-divisional, integrated Global Product Team (GPT) strategy into an efficiently executable plan; predicting and planning solutions to achieve program goals and objectives; driving clarity and removing barriers to ensure team success; interfacing with management and influencing decision-making, proactive management and mitigation of development risks, and ensuring appropriate communication and interface with internal governance. OBJECTIVES: Provides global program management and matrixed leadership to global, cross-functional, cross-divisional teams to drive development and deliver results in early to late-phase major development and/or lifecycle management programs (including established/marketed products) to meet Takeda strategic objectives.
NewSenior Director, Search and Evaluation Lead, Global Oncology Takeda Pharmaceutical Co LtdSenior Director, Search and Evaluation Lead, Global OncologyCambridge, MA$212,000–$333,190 / yearAbout the role: The Senior Director, Oncology Search & Evaluation will be responsible for advancing the oncology portfolio through the integration of external innovation scouting, scientific diligence, and supporting disease area strategy and early asset commercial planning. This leader will drive cross-functional efforts to identify and assess external opportunities, help shape early-stage and pre-commercial asset strategies, and support governance and investment decisions across the oncology portfolio.
Senior Director, National Field Medical Lead Entrada TherapeuticsSenior Director, National Field Medical LeadBoston, MassachusettsRemote$277,000–$317,000 / yearWe are a tight-knit team of experts and leaders in both therapeutic development and rare diseases and are excited to grow and attract colleagues who are ready to join a high-energy, dedicated team that likes to get things done and dramatically improve the lives of patients and their families. Proven experience in working collaboratively and cross functionally across the enterprise of field medical teams, clinical development, commercial, sales, market access and other key functions and demonstrated ability to inform and shape company/product strategy.
NewDirector, HCP Marketing, Bylvay Ipsen SADirector, HCP Marketing, BylvayCambridge, MA$190,500–$265,000 / yearFrom a marketing standpoint, there is a critical need for excellence in strategic planning and excellence in execution to clearly define how we will best drive education of appropriate healthcare providers, deliver successful launches, and innovate for patients in complex and competitive therapeutic areas. The Director, BYLVAY Marketing is a critical member of the brand team, responsible for leading the strategic development and execution of marketing initiatives focused on growing adult segment of the business.
Senior Director, Global Program Lead- Neuroscience Takeda Pharmaceutical Co LtdSenior Director, Global Program Lead- NeuroscienceCambridge, MA$212,000–$333,190 / yearLinks GPT cross-functional sub-teams, such as the Clinical Subteam, Commercial Subteam, Pharmaceutical Sciences (CMC) Subteam, etc. to the GPT through function-based subteam leaders to execute according to the Enterprise GPT Playbook, align and ensure transparency of all program-related activities. Leads key business initiatives: for example, evaluates new opportunities (i.e. in-licensing candidates, impact of change in market conditions or availability of new project data in disease areas where Takeda has little or no previous experience) and provides overall support for feasibility studies on potential global programs-non exhaustive list.
Director, HRBP Ipsen SADirector, HRBPCambridge, MA$210,000–$245,000 / yearOperating in a highly matrixed environment, the role combines strategic leadership, organizational insight, and operational rigor to enable performance, strengthen leadership capability, and drive scalable, sustainable organizational outcomes. This role will work broadly across the North America and GPPS Organizations, providing HR leadership to key global functions and also aligned to the North America business unit-ensuring strong integration between business and functional priorities.
Associate Director, HCP Marketing, Rare Disease / PBC Ipsen SAAssociate Director, HCP Marketing, Rare Disease / PBCCambridge, MA$193,500–$220,000 / yearResponsibilities will encompass traditional HCP marketing as well as peer to peer marketing activities (congresses & speaker bureau), brand planning, development of marketing materials and messages for multichannel engagement focused on advisory boards, educational programs and KOL engagements. The candidate will support U.S. marketing initiatives and key promotional activities to help the Rare team achieve near-term revenue goals and support the ongoing successful launch in rare disease.
Director, Medical Affairs, Rare Disease Ipsen SADirector, Medical Affairs, Rare DiseaseCambridge, MA$225,000–$300,000 / yearThe role also includes oversight of medical information responses (in collaboration with Medical Information), scientific communications (including publications and congress presentations in partnership with the Publication team), and the design and medical oversight of US based clinical studies, as well as the review and approval of promotional and medical materials and educational grants. The Director works closely with the Medical Science Liaison team to guide field medical strategy, develop and maintain relationships with key opinion leaders, and incorporate field insights into medical planning.
Director, Neuroscience Marketing, Migraine Ipsen SADirector, Neuroscience Marketing, MigraineCambridge, MA$190,000–$280,000 / yearMedia Planning & Management: Manage agency partners to establish agency operating models, and develop and execute a comprehensive media strategy that aligns with overall brand objectives; assess performance and optimize investment in external resources. Minimum 15 years of relevant experience, with at least 5 years of pharmaceutical/biotech marketing experience; Experience with Neurotoxins & Migraine is required; preferably 2+ years focused neurotoxin migraine experience.
Senior Director, New Product Strategy & Planning, North America Ipsen SASenior Director, New Product Strategy & Planning, North AmericaCambridge, MA$217,500–$310,000 / yearKnowledge & Experience (essential): A minimum of 10 years' experience in New Product Planning, Global Marketing, Business Development or Portfolio Management roles within the biopharmaceutical industry, including experience in early commercial planning, disease area strategy, business development activity, and forecasting. Be a proactive partner and work collaboratively with cross-functional teams (e.g., business development, external innovation, medical affairs, R&D, regulatory, finance, countries, global pricing & access, business excellence) to support inputs required for commercial modelling & business case development.
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.
Associate Director Global Marketing - Biologics Testing (REMOTE) Charles River Laboratories International IncAssociate Director Global Marketing - Biologics Testing (REMOTE)Wilmington, MARemote$130,000–$150,000 / yearThis role supports our growing and dynamic biologics market, including vaccines, ATMPs (Advanced Therapy Medicinal Products), monoclonal antibodies, and biosimilars, ensuring that Charles River delivers a compelling and differentiated customer experience across the development lifecycle. This leader will design, develop, and implement global marketing strategies aligned with business goals, drive integrated campaign execution, analyze results, and identify new opportunities to strengthen competitive positioning.
Director, Strategic Pricing & Contracting, Value and Access Ipsen SADirector, Strategic Pricing & Contracting, Value and AccessCambridge, MA$190,500–$270,000 / yearOutstanding communication and presentation skills, with polished written and verbal communication skills, good listening skills and an ability to present complex and detailed information in an easy-to-understand manner. Job Description: The Director, Strategic Pricing & Contracting is a key member of the Pricing & Contracting team within the broader Value & Access organization and is primarily responsible for the negotiation and execution of assigned contracts related Payer, Institutional, GPO/Clinic contracts.
Senior Director, Program Management Dyne Therapeutics IncSenior Director, Program ManagementWaltham, MA$233,000–$285,000 / yearThe PM partners closely with the Program Team Leader (PTL) and functional subject matter experts to ensure that plans are in place with appropriate detail and risk awareness to assure successful achievement of the goals of the development team. Maintain clear and open communication with Program Team, Dyne Senior Leadership, and other stakeholders regarding program status, priorities, risks and needs, and facilitate appropriate strategic decision-making.
Director, New Products Strategy Innovation Ipsen SADirector, New Products Strategy InnovationCambridge, MA$190,000–$255,000 / yearBe a proactive partner and work collaboratively with cross-functional teams (e.g., business development, external innovation, medical affairs, R&D, regulatory, finance, countries, global pricing & access, business excellence) to support inputs required for commercial modelling launch dates, LOE, duration of treatment, LCM indications etc. Knowledge & Experience (essential): Significant experience in early commercial or BD roles within a pharmaceutical or biopharmaceutical industry at global level, or Strategy Consulting experience in life sciences (including work in early-commercial strategy, commercialization, LCM, BD, due diligence, etc.).
Associate Director, Neuroscience Marketing, Migraine Patient Marketing Ipsen SAAssociate Director, Neuroscience Marketing, Migraine Patient MarketingCambridge, MA$165,000–$236,000 / yearThe role will be responsible for developing, managing, and ultimately executing all patient-facing elements of the launch This includes all facets of launch readiness planning, including but not limited to: strategy, positioning, segmentation, messaging, creative campaign development/testing, asset development, media, and budget planning/management. This role is critical to shaping the brand's entry into the migraine space and will key in the development and execution of a comprehensive patient marketing strategy that positions Dysport for success in a competitive and evolving market.
Associate Director, Global Scientific Communications Bicara TherapeuticsAssociate Director, Global Scientific CommunicationsBoston, MassachusettsFICERA specifically addresses a key challenge in solid tumor treatment by enabling immune cell penetration into tumors, reducing fibrosis and immunosuppression while reversing TGF--driven resistance mechanisms - ultimately designed to drive the deep, durable responses that may translate into better outcomes and survival for patients. Founded in 2020, we've built a global team of over 100 employees headquartered in Boston, with a clear focus on advancing our lead asset, ficerafusp alfa, or FICERA - a potentially first-in-class bifunctional EGFR-directed antibody combined with a TGF- ligand trap.
Senior Director, Pharmacology Formation Bio IncSenior Director, PharmacologyBoston, MA$285,000–$400,000 / yearPhD in Pharmacology or a related field with at least 10 years of experience in the biopharmaceutical industry Proven track record in leading pharmacology efforts in late-stage drug development Strong understanding of regulatory requirements for pharmacology studies in support of clinical development Experience in due diligence activities for in-licensing opportunities Excellent communication and leadership skills Ability to work effectively in a fast-paced, cross-functional environment Innovative mindset and enthusiasm for leveraging technology in drug development Thorough knowledge and understanding of drug development and clinical research concepts, practices, and regulations Critical thinker about the legacy assumptions in the clinical research process and able to reimagine processes from the ground up Embraces open conversations and challenges to status quo thinking Solid written and oral communication skills; able to synthesize complex concepts and deliver messages clearly Extensive experience in scientific and clinical due diligence for late-stage assets in therapeutic areas that include metabolic and dermatological conditions Experience interacting with regulatory agencies and familiarity with regulatory requirements for dermatology indications Innovative mindset and enthusiasm for leveraging technology to transform drug development in dermatology. Recognizing that this development bottleneck may ultimately limit the number of new medicines that can reach patients, Formation Bio, founded in 2016 as TrialSpark Inc., has built technology platforms, processes, and capabilities to accelerate all aspects of drug development and clinical trials.
Director, Change Management - Labs of Tomorrow TakedaDirector, Change Management - Labs of TomorrowBoston, Massachusetts$177,000–$278,080 / yearThe incumbent will drive change across the organization, challenge legacy ways of working, identify barriers to adoption, and ensure that transformation efforts result in measurable improvements in research productivity, operational efficiency, decision velocity, and organizational readiness. Expected of 5-7 years of change management experience with experience in early drug discovery (e.g., target identification, hit to-lead stages) and late drug discovery (e.g., candidate stage, preclinical/IND enabling stages) in the capacity as a program manager.
Senior Director, AI Engineering -Agentic AI Platform(Remote Eligible) Capital One Financial CorpSenior Director, AI Engineering -Agentic AI Platform(Remote Eligible)Cambridge, MARemote$286,200–$326,700 / yearIn this role, you will: Partner with a cross-functional team of engineers, research scientists, technical program managers, and product managers to deliver AI-powered products that change how our associates work and how our customers interact with Capital One. Basic Qualifications: Bachelor's degree in Computer Science, Engineering, or AI plus at least 10 years of experience developing or leading AI and ML algorithms or technologies, or Master's degree plus at least 8 years of experience developing or leading AI and ML algorithms or technologies.
National Corporate Accounts Director Ipsen SANational Corporate Accounts DirectorBoston, MA$191,000–$275,000 / yearAdditionally, this role leads a team of Corporate Account Directors and is responsible for building and maintaining strategic relationships with key decision-makers, influencing formulary positioning, and supporting Value & Access strategy including contracting and value communication efforts within an evolving healthcare landscape shaped by consolidation, policy changes, and site-of-care shifts. Job Description: The National Corporate Accounts Director is responsible for developing and executing access strategies across key institutional customers and federal accounts, including integrated delivery networks (IDNs), health systems, Veterans Affairs (VA), Department of Defense (DoD), and other government entities.
Director, US Medical Rheumatology Takeda Pharmaceutical Co LtdDirector, US Medical RheumatologyCambridge, MA$192,400–$302,390 / yearEDUCATION, EXPERIENCE AND SKILLS: Required: Advanced Doctoral Degree (e.g., MD, DO, PhD, PharmD) or other advanced degreed professionals considered depending on past relevant experience, including at least 4 years pharmaceutical industry experience, and/or clinical work, research, or academic endeavors. The role has tactical accountability grounded in science, disease state, and competitive clinical data in support of one or more products, and supports the development, and ongoing updates to relevant product-specific medical strategies, in partnership with the Vice President and Medical Unit.
Senior Medical Director, Paroxysmal Nocturnal Hemoglobinuria (PNH), US Medical Affairs Rare Hematology Alexion Pharmaceuticals IncSenior Medical Director, Paroxysmal Nocturnal Hemoglobinuria (PNH), US Medical Affairs Rare HematologyBoston, MAYou will be responsible for: In collaboration with the medical US and global as well as cross-functional colleagues, the Medical Director will develop and facilitate implementation of the medical (PNH) strategic plan for USMA activities by providing medical leadership, insights and strategy to USMA team across functions for one of Alexion's disease areas of key importance in a highly competitive environment. Under the leadership and in collaboration with Executive Medical Director, providing medical strategic and tactical plans for late phase pipeline program for Rare Hematology as well as future LCM and potential late phase pipeline programs in the therapeutic area.
NewDirector, Accounts TheTeam.comDirector, AccountsBoston, MAFrom high school to college and into young adult life, the team takes an audience-first approach, using unrivaled access to understand the passions and interests of these consumers, generate ideas that resonate, and deliver hyperlocal, culturally relevant engagement at scale. NEXT GEN TEAM's integrated approach allows clients to understand and engage with Gen Z and Millennial consumers through custom research, peer-to-peer, social and digital, experiential, media, and community integration strategies.
(Associate) Director, Drug Product - CMC Centessa Pharmaceuticals, LLC(Associate) Director, Drug Product - CMCBoston, MA$170,000–$195,000 / yearWork closely and collaboratively with cross-functional CMC groups including discovery, nonclinical, clinical, project management, legal, sourcing, supply chain, quality and regulatory, as well as other CMC functions. Excellent communication, interpersonal, and project leadership skills, with the ability to influence stakeholders, manage cross-functional and external relationships, and effectively communicate complex concepts to diverse audiences.
Associate Director, Global Scientific Communications Bicara Therapeutics IncAssociate Director, Global Scientific CommunicationsBoston, MAFICERA specifically addresses a key challenge in solid tumor treatment by enabling immune cell penetration into tumors, reducing fibrosis and immunosuppression while reversing TGF--driven resistance mechanisms - ultimately designed to drive the deep, durable responses that may translate into better outcomes and survival for patients. Founded in 2020, we've built a global team of over 100 employees headquartered in Boston, with a clear focus on advancing our lead asset, ficerafusp alfa, or FICERA - a potentially first-in-class bifunctional EGFR-directed antibody combined with a TGF- ligand trap.
Associate Director, Clinical Assay Strategy, Flu CSL PlasmaAssociate Director, Clinical Assay Strategy, FluWaltham, Massachusetts$179,000–$212,000 / yearThis role is intended for a recognized subject matter expert who understands the scientific, operational, and regulatory evolution of influenza immunogenicity assessment, including HAI, microneutralization (MN), ELLA, and multiplex platforms, and can strategically navigate assay modernization while maintaining regulatory alignment. Headquartered in Melbourne, Australia, with major manufacturing hubs in Holly Springs, NC, and Liverpool, UK, the company operates the world’s largest cell-based vaccine facility and serves as a primary partner to governments for global pandemic preparedness.
Associate Director, Clinical Scientist Zenas BioPharma (USA) LLCAssociate Director, Clinical ScientistWaltham, MA$161,700–$202,200 / yearThis position works closely with Medical Directors to support medical monitoring activities, while partnering cross-functionally with Clinical Operations, Data Management, Biostatistics, Translational Sciences, Medical Affairs, and Regulatory Affairs to translate clinical strategy into operational deliverables and ensure rigorous ongoing review of trial data for quality, safety, and protocol compliance. Zenas' earlier stage programs include ZB021, a clinical-stage, potentially best-in-class, oral, IL-17AA/AF inhibitor; ZB022, a preclinical, potentially best-in-class, oral, brain-penetrant, TYK2 inhibitor; and ZB014, a preclinical half-life extended anti-CD-19 and FcRIIb monoclonal antibody.
Senior Director, Corporate Quality - PV Sarepta Therapeutics Inc.Senior Director, Corporate Quality - PVBedford, MA$222,400–$278,000 / yearThis position will liaise with internal groups such as Pharmacovigilance Operations, Safety Evaluation & Risk Management, and Market Research, as well as external groups including contract auditors in an effort to ensure a high level of quality and consistency across the Sarepta platform; design and oversee the audit strategy; assist the GVP team in identifying and implementing corrective and preventive actions; and enable teams to be inspection ready, in support of a culture of sustainable compliance. Primary responsibilities include: Participate in the development of the internal and external Corporate Quality annual audit plan for GVP, REMS, PV vendors, interfaces, processes and preferred business partners and update the audit plan as needed based on identified risks and priorities.
Clinical Pharmacology Director SunovionClinical Pharmacology DirectorMarlborough, MA$190,500–$238,100 / yearSumitomo Pharma Co., Ltd., is a global pharmaceutical company based in Japan with operations in the U.S. (Sumitomo Pharma America, Inc.), focused on addressing patient needs in oncology, urology, women's health, rare diseases, cell & gene therapies and CNS. Lead Phase 1 and special population clinical pharmacology studies (e.g., FIH, SAD, MAD, DDI, organ impairments, elderly/pediatric, PET/EEG), including protocol input, operational oversight, and interpretation and communication of results.
Director, Regulatory Affairs - Clinical Strategy Azurity Pharmaceuticals IncDirector, Regulatory Affairs - Clinical StrategyWoburn, MABrief Team/Department Description: As a part of the Regulatory Affairs team at Azurity, the Regulatory Affairs Director - Clinical Strategy will conduct in-depth analysis of regulatory and clinical information to develop complex strategies supporting potential drug products for development and commercial drug products for expansion of the Azurity portfolio of medications. Principle Responsibilities: • Development and implementation of clinical regulatory strategies and tactics, including but not limited to, Modeling Informed Drug Development (MIDD), real-world data (RWD)/real-world evidence (RWE), and meta-analysis, for pipeline and commercial assets, while considering FDA and other health authority clinical and regulatory requirements.
Associate Director, Accounts Wasserman Media Group LLC (London)Associate Director, AccountsBoston, MAFrom high school to college and into young adult life, the team takes an audience-first approach, using unrivaled access to understand the passions and interests of these consumers, generate ideas that resonate, and deliver hyperlocal, culturally relevant engagement at scale. NEXT GEN·TEAM's integrated approach allows clients to understand and engage with Gen Z and Millennial consumers through custom research, peer-to-peer, social and digital, experiential, media, and community integration strategies.
National Sales Director IpsenNational Sales DirectorBoston, District of ColumbiaThe NSD will also provide clear direction, motivate the field team, build a healthy competitive environment among commercial field representatives, drive innovation & best practice sharing, and drive pragmatism with the goal to enhance our impact among appropriate customers and patients served. Lead a team of Regional Business Directors to implement sales force productivity initiatives including improving and evolving sales force competencies, design and execution of reward systems, sales force deployment strategies, customer relationship management, and talent development.
Director, Regulatory Affairs – Clinical Strategy Azurity Pharmaceuticals - USDirector, Regulatory Affairs – Clinical StrategyWoburn, MADevelopment and implementation of clinical regulatory strategies and tactics,including but not limited to, Modeling Informed Drug Development (MIDD), real- world data (RWD)/real-world evidence (RWE), and meta-analysis, for pipeline and commercial assets,while considering FDA and other health authority clinical and regulatory requirements. As a part of the Regulatory Affairs team at Azurity, the Regulatory Affairs Director – Clinical Strategy will conduct in depth analysis of regulatory and clinical information to develop complex strategies supporting potential drug products for development and commercial drug products for expansion of the Azurity portfolio of medications.
Director, Toxics Use Reduction Institute (TURI) University of MassachusettsDirector, Toxics Use Reduction Institute (TURI)Lowell, MAGeneral Summary of Position: The Massachusetts Toxics Use Reduction Institute (TURI), a renowned research, practice, and education institute located at UMass Lowell in the Zuckerberg College of Health Sciences, is seeking a collaborative leader to serve as its next Director, and to provide strategic, organizational, and fiscal leadership to the Institute. It does this by promoting adoption of toxics use reduction, pollution prevention, and safer chemistry through education and training, policy advocacy, research, laboratory services, provision of information and technical support for companies and communities, and grants to industry, academic researchers, and community and governmental organizations.
Director, Commercial Insights & Analytics - PNH Alexion Pharmaceuticals IncDirector, Commercial Insights & Analytics - PNHBoston, MAThe annual base pay for this position ranges from US $194,571 & $291,856 Our positions offer eligibility for various incentives-an opportunity to receive short-term incentive bonuses, equity-based awards for salaried roles and commissions for sales roles. Forecasting leadership: Build US long-term patient-based and US short-term TRx/NBRx forecasting models that synthesize robust inputs, benchmark against analogs, and align with US and key market assumptions.
NewAssociate Director Product Design Chewy IncAssociate Director Product DesignBellevue, MA$166,000–$265,000 / yearAbility to lead design for multiple tools and large-scale initiatives involving multiple business groups; Communication & Collaboration; Strong communication, presentation, and social skills. As a team of hard-working, collaborative, and fun-loving designers, researchers, and builders, we're looking for creative and driven talent to join the pack.
Director, Outreach and Policy Boston Public Health CommissionDirector, Outreach and PolicyMADetermines the overall strategies of the specific projects under their supervision (e.g., a PR or marketing campaign) and ensures that all internal and external communications related to them align tightly with OVS goals. The Director, Outreach and Policy will be responsible for developing the Veterans' Services outreach strategies and directly managing outreach activities that promote and enhance Veterans' engagement and military affairs.
Director, Accounting and External Reporting Editas Medicine IncDirector, Accounting and External ReportingCambridge, MAOperating at the intersection of technical accounting, SEC reporting, and operational execution, this individual will lead a scalable, high-performing accounting and external reporting function that delivers accurate, timely, and compliant financial reporting while strengthening operational rigor, developing talent, and modernizing processes through automation, systems optimization, and practical AI applications over the next 1218 months. Serve as the lead point of contact for internal and external auditors, ensuring efficient audit coordination, timely issue resolution, strong stakeholder communication, and successful completion of audit and compliance activities with minimal disruption to the business.
Director, Communications & Brand Verint Systems, Inc.Director, Communications & BrandBoston, MAOverview of Job Function: The Director, Communications and Brand will partner with the senior leadership to develop, direct and oversee the global communications strategy, planning and execution. + A minimum of 8 years of progressive leadership experience leading teams within one or more similar lines of business, which may include marketing or marketing operations.
NewDirector, Electronic Trading Product FidelityDirector, Electronic Trading ProductBoston, MassachusettsRemoteDE leveraging Transaction Cost Analysis (TCA) - pre- and post-trade transaction cost models - to compare, contrast, and analyze performance of trading algorithms for clients, including Liquidity Seeking, Percent-of-Volume, Dark, Implementation Shortfall, VWAP, TWAP, and CLOSE; designing and implementing algorithm scheduling, allocation, pricing, and lit/dark counterparty detection features to reduce trading costs; developing deep market structure knowledge, integrating various Trajectory Cross venues and Private Room liquidity in algos, to enhance trading strategies and optimize order placement. Skills and Knowledge : Candidate must also possess: Demonstrated Expertise (“DE”) analyzing and designing systems to build quantitative models for systematic trading using R and Python; developing time series forecasting models, multi-asset class portfolio construction strategies, risk management tools, alpha research, and simulation-based algorithms to build investment strategies using R, Python, and Kdb+/Q with tick-level market data; and building automated diagnostic reporting processes for model risk management using R and Python.
Director Municipal Services Town of DuxburyDirector Municipal ServicesDuxbury, MA$111,192–$150,109 / yearRecommended Minimum Qualifications: Education and Experience: Five or more years of prior work experience in the supervision of building construction or design, in the construction trades, a Bachelor’s degree in a related field; Experience with operational and capital budget development and Energy Services contracting, or any equivalent combination of education, training and experience which provides the required knowledge, skills and abilities to perform the essential functions of the job. Employee conducts periodic inspections, maintains records, and issues Certificates of Inspection for existing buildings as required by statute including; places of assembly such as night clubs, restaurants, meeting halls, churches and schools, and for institutional uses, such as hospitals, nursing homes, jails and prisons, and residential uses, such as hotels, lodging houses, limited group residences and all multifamily structures.
Associate Director Regulatory Affairs – Vascular (on-site) AbbottAssociate Director Regulatory Affairs – Vascular (on-site)Westford, Massachusetts$129,300–$258,700 / yearMaintains expert working knowledge of laws, regulations and enforcement decisions related to Quality Assurance (QA), manufacturing and Research & Development (R&D) issues that may impact company operations and decision making; communicates such knowledge to all internal stakeholders. As a manager, the function of an Associate Director, Regulatory Affairs is to combine knowledge of scientific, regulatory and business issues to enable products that are developed, manufactured or distributed to meet required legislation.
Director, Market Access and Channel Strategy US GI & Immunology TakedaDirector, Market Access and Channel Strategy US GI & ImmunologyBoston, Massachusetts$177,000–$278,080 / yearEnsures close collaboration with other Managed Markets colleagues along with Medical, HEOR, Marketing, Finance, Analytics and Sales colleagues to capture relevant payer insights, identify data gaps, develop compelling value propositions for field-based teams. Demonstrated success in development/execution of targeted briefings for executive leadership, senior management and business leaders; Well organized, highly motivated, innovative, process driven, results oriented; and outstanding oral and written communications skills.
Director, U.S. HCP Marketing Strategy, Rare Hematology Alexion Pharmaceuticals IncDirector, U.S. HCP Marketing Strategy, Rare HematologyBoston, MA$194,126.40–$291,189.60 / yearWorking collaboratively across US commercial team, with close collaboration with Patient marketing director aHUS/TMA and AD digital marketing aHUS/TMA, as well as key cross functional partners like global team, medical affairs, market access, patient advocacy, legal and compliance to support flawless execution of launch planning for HSCT-TMA. This is what you will do: As part of the Hematology and Nephrology (Hem/Neph) U.S. commercial team, the Director, U.S. HCP Marketing Strategy, HSCT-TMA will report to the marketing lead aHUS/TMA and partners with the US cross-functional and global teams to drive HSCT-TMA strategies and tactics.
Director, Global Patient Advocacy Lead Alexion Pharmaceuticals IncDirector, Global Patient Advocacy LeadBoston, MA$151,753–$227,630 / yearJoining 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.
Associate Director Finance Flagship Pioneering IncAssociate Director FinanceCambridge, MA$148,000–$203,500 / yearProvide accounting and controllership support for PM, Flagship Labs, or related portfolio company needs as required, including GAAP compliance, audit support, financial statement review, close process support, ASC 842 lease accounting, capital project tracking, and accounting policy or process implementation. While this role is primarily focused on the Pioneering Medicines business unit, the successful candidate should also bring strong accounting and controllership capabilities and be able to provide cross-functional support to Flagship Labs or related portfolio company finance teams as business needs require.
Associate Director, Clinical Supplies Project Manager Moderna IncAssociate Director, Clinical Supplies Project ManagerCambridge, MA$142,500–$256,500 / 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. The scope includes the operational planning and strategy required to execute end-to-end supply management, including demand planning, label development, packaging/labeling, distribution, IRT UAT/supply management, temperature excursions, and site activations.