Associate Director, Customer Master Lead Vertex PharmaceuticalsAssociate Director, Customer Master LeadBoston, Massachusetts$160,000–$240,000 / yearWe are seeking an execution-focused Associate Director, Customer Master to lead the Customer(HCP/HCO) master data domain within Vertex’s Enterprise Master Data Management (MDM) organization reporting to the Director, Enterprise MDM. Strong knowledge of healthcare customer reference data and industry data sources supporting HCP/HCO mastering, including OneKey, MedPro, SP/SD data, as well as affiliations, hierarchies, and golden record creation.
Vice President, Pharmaceutical Development Kymera TherapeuticsVice President, Pharmaceutical DevelopmentWatertown, MA$315,000–$395,000 / yearHaving advanced the first degrader into the clinic for immunological diseases, Kymera is focused on building an industry-leading pipeline of oral small molecule degraders to provide a new generation of convenient, highly effective therapies for patients with these conditions. Foster strong cross-functional partnerships across Research, Clinical, Regulatory, Quality, Supply Chain, and Program Management to enable efficient advancement of pipeline programs.
Associate Director / Director, Medical Information Cognito TherapeuticsAssociate Director / Director, Medical InformationCambridge, MassachusettsPartner closely with Medical Affairs, Field Medical, Scientific Communications, Clinical Development, Pharmacovigilance/Drug Safety, Quality, Commercial, Market Access, Patient Support, and other functions to support compliant scientific exchange and launch readiness. Serve as the internal subject matter expert on MI best practices, regulatory expectations (FDA, EMA/MDR/Notified Bodies), and industry benchmarks for neurocognitive disease and advanced therapies.
Senior Specialist or Manager, Quality Systems Kymera TherapeuticsSenior Specialist or Manager, Quality SystemsWatertown, MA$85,000–$200,000 / yearThe individual will play a key role in sustaining day-to-day QMS operations, managing the controlled document lifecycle including biennial review programs, driving training compliance across the organization, and supporting quality systems performance monitoring as Kymera advances late-stage development and commercialization. Having advanced the first degrader into the clinic for immunological diseases, Kymera is focused on building an industry-leading pipeline of oral small molecule degraders to provide a new generation of convenient, highly effective therapies for patients with these conditions.
NewIT Director, Development Business Partner Kymera TherapeuticsIT Director, Development Business PartnerWatertown, MA$195,000–$275,000 / yearReporting to the Senior Director of IT Applications, this person will own the technology strategy and execution across the Development portfolio, build trusted partnerships with Clinical Operations, Clinical/Medical Development, Quality, Biometrics, Data Management, Regulatory, and more, and serve as a thought partner to the IT leadership team as Kymera scales. Having advanced the first degrader into the clinic for immunological diseases, Kymera is focused on building an industry-leading pipeline of oral small molecule degraders to provide a new generation of convenient, highly effective therapies for patients with these conditions.
Associate Director Medical Writing (Hybrid) Vertex Pharmaceuticals, IncAssociate Director Medical Writing (Hybrid)Boston, MA$157,600–$236,400 / yearAt 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. This role applies advanced technical expertise and develops solutions to complex problems, fosters interdisciplinary understanding, and integrates Medical Writing Science department activities with those of other departments.
Lead Clinical Research Associate Alira HealthLead Clinical Research AssociateBoston, MA$110,000–$130,000 / yearLead CRAs work closely with US: Director of Clinical Monitoring, In-house CRAs, field CRAs, EU: Associate Director of Clinical Monitoring, CRAs, CTCs and Clinical Project Managers to ensure protocol compliance, address site questions, and assist with study recruitment, site training, and other site-related issues. Prepares consistently accurate and timely monitoring visit reports documenting site-related problems, resolutions, actions taken, protocol deviations, study progress, and enrollment status.
Research Associate II, Bioanalytical Keros TherapeuticsResearch Associate II, BioanalyticalLexington, MA$62,000–$87,000 / yearWith a focus on developing differentiated product candidates that are designed to alter TGF- signaling, we aim to target the pathways critical for the growth, repair and maintenance of blood cells and a number of tissues, including bone, skeletal muscle, adipose and heart tissue. Bachelor's degree in cell biology, molecule biology, biochemistry, immunology, or related field with 0 to 2 years of relevant experience in an industrial pharmaceutical/biotechnology lab setting.
Director, Knowledge Graph & Semantics - Hybrid Role Vertex Pharmaceuticals, IncDirector, Knowledge Graph & Semantics - Hybrid RoleBoston, MARemote$216,400–$324,600 / yearWe are seeking an experienced engineering leader to build and operate Vertex's enterprise Knowledge Graph and Semantic Layer: the unified, navigable representation of Vertex's data, concepts, and relationships that AI agents and analytical systems traverse to reason over our business. Design, build, and operate Vertex's enterprise knowledge graph spanning clinical, research, regulatory, and commercial domains, including ingestion, storage, query, and lifecycle management of nodes, edges, and properties.
Director, Knowledge Graph & Semantics - HYBRID ROLE Vertex PharmaceuticalsDirector, Knowledge Graph & Semantics - HYBRID ROLEBoston, MassachusettsRemote$216,400–$324,600 / yearWe are seeking an experienced engineering leader to build and operate Vertex's enterprise Knowledge Graph and Semantic Layer: the unified, navigable representation of Vertex's data, concepts, and relationships that AI agents and analytical systems traverse to reason over our business. Design, build, and operate Vertex's enterprise knowledge graph spanning clinical, research, regulatory, and commercial domains, including ingestion, storage, query, and lifecycle management of nodes, edges, and properties.
NewAssociate Counsel, Contracting Les Laboratoires Servier SASAssociate Counsel, ContractingBoston, MA$189,000–$224,000 / yearDraft, review, negotiate, and finalize a broad range of agreements supporting all business functions, with particular focus on R&D-related agreements, including CDAs, consulting agreements, MSAs, SOWs, clinical trial agreements, sponsored research agreements, research collaborations, material transfer agreements, vendor and CRO agreements, work orders, change orders, sponsorships, grants, data use and transfer arrangements, privacy and data processing agreements, SaaS/IT licenses, amendments, and other business-critical contracts. 4-7+ years of relevant legal experience, including experience in the biopharmaceutical, pharmaceutical, biotechnology, healthcare, or life sciences industry, with demonstrated experience drafting and negotiating a broad range of agreements across business functions and preferred experience with R&D, clinical development, or research-related contracting.
Senior Director, Quality Repligen CorporationSenior Director, QualityWaltham, Massachusetts$191,250–$260,000 / yearAs a member of the Global Quality Leadership Team, reporting directly to the VP Global Quality, you will partner closely with Operations, Commercial, Product Management, Supply Chain, Regulatory Affairs, and senior business leaders to establish a culture of quality excellence, operational performance, and continuous improvement throughout the network. Lead and execute the quality strategy across Repligen’s Filtration & System networks, with accountability for Quality Assurance, Quality Systems, Quality Compliance, Validation, Quality Control, Supplier Quality partnership, and Customer Quality activities.
Senior Manager, Marketing Operations & Technology (REMOTE) Charles River Laboratories International IncSenior Manager, Marketing Operations & Technology (REMOTE)Wilmington, MARemote$103,000–$145,000 / yearIf you are interested in applying to Charles River Laboratories and need special assistance or an accommodation due to a disability to complete any forms or to otherwise participate in the resume submission process, please contact a member of our Human Resources team by sending an e-mail message to crrecruitment_US@crl.com. With over 20,000 employees within 110 facilities in over 20 countries around the globe, we are strategically positioned to coordinate worldwide resources and apply multidisciplinary perspectives in resolving our client's unique challenges.
Medical Director, Oncology Clinical Development - Lung & Head/Neck Cancers GSK plcMedical Director, Oncology Clinical Development - Lung & Head/Neck CancersWaltham, MA$222,750–$371,250 / yearAnalytical Thinking, Clinical Data Interpretation, Clinical Development, Clinical Pharmacology, Clinical Trial Designs, Clinical Trials Monitoring, Digital Fluency, Drug Regulatory Affairs, Evidence Based Decision Making, Executive Presence, Hematology and Oncology, Learning Agility, Matrix Leadership, Real World Evidence (RWE), Scientific Presentations. Use medical expertise to contribute to the end to end (protocol concept to final study report) to ensure scientific integrity and timely delivery of clinical trials which ensure consistency with the clinical development strategy for regulatory approvals, reimbursable medicines, and successful lifecycle management; demonstrate ability to incorporate global considerations into decision making.
SERM Senior Medical Director, Oncology GSK plcSERM Senior Medical Director, OncologyWaltham, MA$284,625–$474,375 / yearGSK fosters a culture ambitious for patients, accountable for impact, and committed to doing the right thing, making sure that we focus our efforts on accelerating significant assets that meet patients' needs and have the highest probability of success. Clinical Development, Drug Regulatory Affairs, Evidence Based Decision Making, Good Clinical Practice (GCP), Influencing Without Authority, Learning Agility, People Management, Project Management, Scientific Presentations, Strategic Thinking.
Associate Director, Quality Systems and Compliance Beam Therapeutics IncAssociate Director, Quality Systems and ComplianceCambridge, MA$185,000–$225,000 / yearBeam's suite of gene editing technologies is anchored by base editing, a proprietary technology that is designed to enable precise, predictable and efficient single base changes, at targeted genomic sequences, without making double-stranded breaks in the DNA. Responsibilities: Qualification: Lead and manage both the onboarding and qualification process for new and existing commercial suppliers (e.g., treatment centers and transportation providers), including pre-classifications and quality system evaluations/reevaluations including identification of quality risks and development of mitigation strategies.
Director, Drug Product Formulations Rhythm Pharmaceuticals IncDirector, Drug Product FormulationsBoston, MA$182,000–$275,000 / yearAs Director, Drug Product - Formulation, you will lead the global strategy and execution of oral drug product development across all phases, from early development through commercialization and lifecycle management. Direct process development, scale-up, and manufacturing of oral dosage forms (e.g., blending, granulation, compression, coating, encapsulation, spray drying, hot-melt extrusion), including support for innovative technologies where applicable.
Senior Director, Biotherapeutics Manifold Bio IncSenior Director, BiotherapeuticsBoston, MAThis role spans discovery and nonclinical development, including optimal utilization of internal protein science expertise to run high-throughput in vivo screens, bioengineering strategies to generate best-in-class molecules, and oversight of external contract manufacturing organizations (CDMOs) to develop processes and manufacture drug product for clinical trials. Our in vivo-centric discovery platform produces millions of experimentally validated protein designs per campaign, creating the datasets that make our models possible and our approach uniquely powerful.
Associate Director, Clinical Supply Chain Management Stoke Therapeutics, Inc.Associate Director, Clinical Supply Chain ManagementBedford, MA$182,000–$199,000 / yearWork with the clinical team to configure and set up Interactive Response Technology (IRT) Systems including automated randomization and drug supply management, including specification design, implementation, and user acceptance testing (UAT) for IRT systems, ensuring effective tracking, randomization, and inventory management. The Stoke Therapeutics team is seeking an experienced and driven Associate Director, Clinical Supply Chain to lead the planning, forecasting, and execution of clinical supply strategies that ensure uninterrupted drug availability throughout global clinical trials.
Senior Director, Revenue & Government Pricing Amylyx PharmaceuticalsSenior Director, Revenue & Government PricingCambridge, MARemote$236,000–$266,000 / yearThe individual will partner closely with Commercial, Market Access, Legal, Accounting, FP&A, IT, Executive Leadership, and external vendors to drive scalable and compliant business processes while providing analytical and strategic leadership that informs pricing decisions, supports commercial strategy, and optimizes long-term revenue. As a key leader within a growing Finance organization, the Senior Director, Revenue & Government Pricing will have end-to-end responsibility for revenue accounting, gross-to-net operations, government pricing compliance, and oversight of key outsourced service providers supporting revenue operations and government pricing.