Executive Medical Director, CardioRenal Eli Lilly and CoExecutive Medical Director, CardioRenalBoston, MA$243,000–$356,400 / yearCollaborate with the Preclinical groups, Clinical Pharmacology, Health Outcomes and New Product Planning in the development and maintenance of Draft Launch Labels and Value Propositions that address key customer needs (patient, provider, and payer); are consistent with known biological characteristics and effects of the molecule; consider all appropriate clinical strategies, development plans and study protocol designs. The Executive Director; leveraging her/his scientific training, clinical expertise, and relevant experience; will work with preclinical teams to develop sound preclinical strategies to progress molecules to first-in-human trials and develop sound clinical development strategies and trials across all phases of development consistent with best clinical practices.
NewSenior Director of Child Welfare Slalom IncSenior Director of Child WelfareBoston, MA$248,000–$325,000 / yearSlalom Leadership - Leads and develops teams, individuals, and self by creating a safe space where people feel comfortable being authentic and can share diverse perspectives in conversations; coach and mentor others; and ensure the team delivers on results and holds the team accountable to results. Partnerships and Alliances - Cultivate relationships and GTM strategies with alliance partner Child Welfare industry executives (such as the Public Health leaders at AWS, Microsoft, Salesforce, Google, Snowflake, and others), and with small women and minority owned business partners.
Director, Molecular AI & Federated Learning Eli Lilly and CoDirector, Molecular AI & Federated LearningBoston, MA$177,000–$281,600 / yearBenchmarking, Dissemination & Governance: Establish rigorous benchmarks using public (ChEMBL, ZINC, PubChem) and proprietary Lilly data; author high-impact publications (e.g., NeurIPS, ICML, ICLR) and deliver compelling presentations to internal and external audiences; and uphold reproducible code, internal libraries, and version control for data, code, and models. Our current groups include: Africa, Middle East, Central Asia (AMECA), Black Employees at Lilly (BE@Lilly), Chinese Culture Network (CCN), EnAble, Evolve, Lilly Indian Network (LIN), Organization of Latinx at Lilly (OLA), Pride (LGBTQ+ Allies), Veterans Leadership Network (VLN) and Women's Initiative for Leading at Lilly (WILL).
Director, Consulting VynamicDirector, ConsultingBoston, Massachusetts$170,000–$200,000 / yearOur expertise spans offerings including strategic planning & mobilization (SP&M), operating model & organization design (OMOD), deal activation & partnership enablement (DAPE), product launch strategy & planning, customer experience transformation, tech & digital transformation, strategic project management office, and change management. From early-stage development to loss of exclusivity, we simplify complexity, unlock value, and make collaboration seamless at every pivotal moment – supporting confident, insight-driven decisions that move innovation forward.
Director/Senior Director, G&A Digital Business Partner Obsidian Therapeutics IncDirector/Senior Director, G&A Digital Business PartnerCambridge, MA$206,000–$275,000 / yearAs a member of our Digital Solutions & Technology team, you will be a vital part of a highly collaborative group working to unlock the promise of precision cell therapy for patients, starting with our lead program amsoki-cel (OBX-115), a novel engineered tumor-infiltrating lymphocyte (TIL) cell therapy that uses our proprietary cytoDRiVE platform. We are looking for a highly motivated Director/Senior Director, G&A IT Digital Business Partner with a strong background in enterprise business systems, finance systems ownership and public-company SOX ITGC execution.
Director, Drug Development AI Nexus Decision Integration Lead Bristol-Myers Squibb CoDirector, Drug Development AI Nexus Decision Integration LeadCambridge, MA$251,570–$304,839 / yearThis individual will serve as the primary bridge between Drug Development, Research and the AI Nexus team, translating strategic priorities, business requirements, and decision-making needs into AI-enabled workflows, governance processes, data requirements, and platform capabilities that improve the quality, speed, and consistency of development decisions. Working in close partnership with BI&T, Research, and functional leaders, the role will drive strategic prioritization, workflow redesign, AI-data readiness, adoption, and organizational change to enable new ways of working.
Director, Intellectual Property DecipheraDirector, Intellectual PropertyWaltham, MA$218,000–$300,000 / yearROMVIMZA (vimseltinib) is a kinase inhibitor approved in the United States for adult patients with symptomatic tenosynovial giant cell tumor (TGCT) for which surgical resection will potentially cause worsening functional limitation or severe morbidity, and in the European Union for adult patients with TGCT associated with clinically relevant physical function deterioration and in whom surgical options have been exhausted or would induce unacceptable morbidity or disability. In addition to advancing multiple product candidates from Deciphera's platform in clinical studies, QINLOCK (ripretinib) is Deciphera's switch-control kinase inhibitor approved in many countries including the European Union and the United States for the treatment of adult patients with advanced gastrointestinal stromal tumor (GIST) who have received prior treatment with 3 or more kinase inhibitors, including imatinib.
Senior Director, Program Lead DecipheraSenior Director, Program LeadWaltham, MA$226,200–$310,000 / yearROMVIMZA (vimseltinib) is a kinase inhibitor approved in the United States for adult patients with symptomatic tenosynovial giant cell tumor (TGCT) for which surgical resection will potentially cause worsening functional limitation or severe morbidity, and in the European Union for adult patients with TGCT associated with clinically relevant physical function deterioration and in whom surgical options have been exhausted or would induce unacceptable morbidity or disability. In addition to advancing multiple product candidates from Deciphera's platform in clinical studies, QINLOCK (ripretinib) is Deciphera's switch-control kinase inhibitor approved in many countries including the European Union and the United States for the treatment of adult patients with advanced gastrointestinal stromal tumor (GIST) who have received prior treatment with 3 or more kinase inhibitors, including imatinib.
Senior Director, Market Access - Lilly Regenerative Medicine (LRM) Eli Lilly and CompanySenior Director, Market Access - Lilly Regenerative Medicine (LRM)Us, Massachusetts$181,500–$266,200 / yearOur current groups include: Africa, Middle East, Central Asia (AMECA), Black Employees at Lilly (BE@Lilly), Chinese Culture Network (CCN), EnAble, Evolve, Lilly Indian Network (LIN), Organization of Latinx at Lilly (OLA), Pride (LGBTQ+ Allies), Veterans Leadership Network (VLN) and Women’s Initiative for Leading at Lilly (WILL). The Senior Director, Market Access is LRM's senior strategic owner of global market access strategy across the gene therapy portfolio — including ultra-rare disease assets and common-disease assets such as wet AMD.
Director, Medical Safety Assessment Physician Bristol-Myers Squibb CoDirector, Medical Safety Assessment PhysicianMA$286,560–$347,244 / yearOversee, prepare and/or review aggregate safety review documents (eg, Development Safety Update Reports [DSUR], Periodic Benefit-Risk Evaluation Reports [PBRER]) and safety sections of relevant clinical trial documents (eg, protocols, clinical study reports [CSR], investigator brochures [IB], informed consent forms [ICF]) and regulatory filings (eg, clinical trial applications [CTA], marketing authorization applications [MAA]). Based on eligibility*, additional time off for employees may include unlimited paid sick time, up to 2 paid volunteer days per year, summer hours flexibility, leaves of absence for medical, personal, parental, caregiver, bereavement, and military needs and an annual Global Shutdown between Christmas and New Years Day.
Director of Scientific Communications & Evidence Generation Genetix Biotherapeutics IncDirector of Scientific Communications & Evidence GenerationSomerville, MA$225,000–$255,000 / yearPosition Summary: The Director of Scientific Communications & Evidence Generation will be responsible for developing a plan for disseminating the company's scientific data (manuscripts, abstracts, posters, presentations); as well as identifying clinical evidence gaps, overseeing non-registrational research, and collaborating with cross-functional teams to generate real-world evidence (RWE), health economics and outcomes research (HEOR), and investigator-sponsored research (ISR) to support product value and safety profiles. Data Generation: Lead the development of an integrated evidence generation plan (IEGP) aligned with overall medical affairs goals to address unmet needs in collaboration with Clinical Development, Regulatory, HEOR, and Commercial teams to avoid duplicative efforts.
Director of Digital & Product Management American Consumer Credit CounselingDirector of Digital & Product ManagementNewton, MA$150,000 / yearOperating within ACCCs operating system, the Director owns the Digital & Product Management function on the accountability chart and is responsible for establishing clear priorities, rocks, scorecard measures, operating rhythms, and team accountabilities. This role owns the digital product roadmap and provides leadership across the full product lifecycle from discovery and prioritization through design, development, testing, implementation, adoption, performance management, and continuous improvement.
Associate Director, US Accounting & Reporting GaldermaAssociate Director, US Accounting & ReportingBoston, MA$180,000–$210,000 / yearCoordinate with business unit finance partners to ensure key estimates and judgments are clearly documented in accordance with IFRS, including completion of quarterly assessments for projected revenue recognition accruals and corresponding lookback analyses once actual data is available. The Associate Director, US Accounting & Reporting will manage a team of 4 direct reports, oversee the work of GBS (Genpact) team members, and partner closely with US Finance leaders, Group Accounting, and cross-functional teams.
Associate Director, Engineering Projects Novo Nordisk ASAssociate Director, Engineering ProjectsLexington, MA$175,000–$225,000 / yearThis role has direct reporting line to the Head of US R&D Operations and a dotted reporting line to Head of R&D Investments (CAPEX) and will have collaborative and cross-functional relationships/responsibilities with onsite Facilities and Lab Operations, Global R&D IPG, North America and NN Global teams. As a member of the US R&D Facilities Leadership Team, the Associate Director is accountable for capital strategy, operations engineering governance and project oversight ensuring projects progress from concept through approval, execution and close-out while meeting business, regulatory, quality and operational requirements.
Senior Director of Electrical Engineering TransMedicsSenior Director of Electrical EngineeringAndover, MassachusettsHands-on experience designing, testing, and formally verifying digital and analog systems, including electrostimulation or ECG monitoring, microprocessor-based electromechanical designs, analog front-end data acquisition, motor control, communications interfaces, power supplies, and battery controller design. TransMedics is scaling fast, and the electrical engineering organization needs a leader who can build the team, systems, and capabilities to match that growth—while staying close enough to the technical details to step into a design review, unblock a verification failure, or work a supplier issue personally when it matters.
New England Business Development Director Daniels HealthNew England Business Development DirectorBoston, MAFull timeThis role is key to driving new business within the acute care market (hospitals), with a focus on growing our client base and strategically expanding our book of business. Produce reports on the territory successes and areas requiring development in conjunction with the Account Manager, constantly review all sales activities, targets, and strategies in order to maximize results.
Director, Alliances & Channel Sales CoralogixDirector, Alliances & Channel SalesBoston, MA$250,000–$400,000 / yearCoordinate and lead joint workshops with our AEs, SEs, and prospects — architecture sessions, migration assessments, cost-modeling deep dives. Someone who sits in the SI's practice meetings, gets Coralogix into the reference architecture, walks the partner's AE into our AE's pipeline, and then stays in the deal until it closes.
NewSenior Director, Manufacturing Engineering TransMedicsSenior Director, Manufacturing EngineeringAndover, MassachusettsDirector of Manufacturing Engineering is a pivotal leadership role within TransMedics Supply Chain organization, leading Advanced Operations (New Product & Technology Introduction), Sustaining Engineering, Manufacturing (Process) Engineering, and Technical Field Service. To accomplish this mission, we partner closely with transplant stakeholders worldwide and help expand their access to healthy donor organs, while delivering the highest quality technology, service, clinical care and outcomes.
NewDirector - Group Living Environment (GLE) Riverside Community CareDirector - Group Living Environment (GLE)Dedham, 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 in 2022 and a best-in-state employer by Forbes. The GLE Director exemplifies the values inherent in recovery-oriented services, including creating a respectful work environment, engaging in ongoing learning, and participatingin continuous quality improvement.
Director, Regulatory CMC Genetix Biotherapeutics IncDirector, Regulatory CMCSomerville, MA$220,000–$235,000 / yearThe Director, Regulatory CMC is responsible for leading execution of global CMC regulatory strategies for approved and late-stage gene therapy products, with a primary focus on lifecycle management, change management, and regulatory compliance. This role supports the development and delivery of post-approval regulatory strategies and ensures effective implementation of manufacturing, analytical, and control changes across global markets.