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 PharmaceuticalsAssociate Director Medical Writing (Hybrid)Boston, Massachusetts$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.
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.
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.
Senior Director, Quality Repligen CorporationSenior Director, QualityWaltham, MassachusettsMake a global impact—join Repligen. We’re united by a mission to inspire advances in bioprocessing as a preferred partner in the production of biologic drugs that improve human health worldwide. No matter your role or background, at Repligen, you will play a key part in shaping some of the most innovative and life-changing th...
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.
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.
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.
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.
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.
Raven StealthCo - Scientist, Conjugation Chemistry RavenRaven StealthCo - Scientist, Conjugation ChemistryBoston, MassachusettsKey qualifications for the Scientist, Conjugation Chemistry include: A degree (BS/MS/PhD) in chemistry, protein engineering, or a related discipline with 3+ years of experience working with antibody, protein, or peptide conjugates in the biopharmaceutical industry; title will be commensurate with level of qualifications and experience. The Scientist, Conjugation Chemistry will report directly to the Director of Oligonucleotide and Conjugation Chemistry and will interface frequently with members of the delivery group and cross-functional teams to advance oligonucleotide therapeutic programs.
Director, Agent Intelligence - HYBRID ROLE Vertex PharmaceuticalsDirector, Agent Intelligence - HYBRID ROLEBoston, MassachusettsRemote$216,400–$324,600 / yearYou will own the four primitives that all Vertex agents are built from: agent memory (personal and organizational), personas as code, skills (atomic tools and higher-order compositions), and the flagship agents that put those primitives to work on Vertex's hardest use cases. Design, build, and deploy custom AI agents for Vertex's highest-value enterprise use cases using Snowflake Cortex AI, Databricks AI, and agent orchestration frameworks, using these builds to harden the underlying primitives.
Lab Automation Engineer Vertex Pharmaceuticals, IncLab Automation EngineerBoston, MA$85,600–$128,400 / yearEducation and Experience: Typically requires a Bachelor's Degree in chemical engineering, computer sciences or related field and 1 years experience in life sciences, engineering or academia. The Lab Automation Engineer will be a part of a team dedicated to designing, implementing, and validating automation solutions, across various automation platforms (Hamilton/Biomek/etc.), with a moderate degree of supervision.
Associate Director, Salesforce Architect Vertex Pharmaceuticals, IncAssociate Director, Salesforce ArchitectBoston, MA$170,400–$255,600 / yearUnderstand system architecture and technical needs, create, analyze, and validate detailed architectural, functional and technical specifications, facilitate architecture and design sessions with cross functional and development teams to define and align on the solution, systems architecture, design, and other SLC/GxP deliverables. Leverage strong communication and analytical skills, technical expertise to understand, document, assess, and drive technical architecture/design needs to accelerate process enhancement and operational efficiencies.
Raven StealthCo- Director, Oligonucleotide and Conjugation Chemistry RavenRaven StealthCo- Director, Oligonucleotide and Conjugation ChemistryBoston, Massachusetts$210,000–$235,000 / yearBuild internal lab capabilities and lead a team of conjugation and analytical scientists to prepare, purify, and analytically characterize oligonucleotide conjugates, particularly antibody-oligonucleotide conjugates. As such, the Director, Oligonucleotide and Conjugation Chemistry should be highly nuanced in terms of their interpersonal style and able to lead and work effectively within a highly collaborative, entrepreneurial, and fast-paced start-up environment.
Director, Agent Intelligence - Hybrid Role Vertex Pharmaceuticals, IncDirector, Agent Intelligence - Hybrid RoleBoston, MARemote$216,400–$324,600 / yearYou will own the four primitives that all Vertex agents are built from: agent memory (personal and organizational), personas as code, skills (atomic tools and higher-order compositions), and the flagship agents that put those primitives to work on Vertex's hardest use cases. Design, build, and deploy custom AI agents for Vertex's highest-value enterprise use cases using Snowflake Cortex AI, Databricks AI, and agent orchestration frameworks, using these builds to harden the underlying primitives.
Territory Sales Representative Inizio EngageTerritory Sales RepresentativeBoston, MassachusettsThis role is responsible for developing and executing territory business plans, cultivating strategic customer relationships, and driving education and awareness of our client’s portfolio across hospitals, integrated delivery networks (IDNs), academic medical centers, specialty pharmacies, physician offices, outpatient infusion centers, and home infusion providers. This position requires strong territory management skills, the ability to navigate complex healthcare organizations, and a customer-focused approach to identifying opportunities, supporting clinical education, and delivering value to healthcare professionals and key decision-makers.
Associate Director / Director, Medical Information Cognito Therapeutics IncAssociate Director / Director, Medical InformationCambridge, MAPartner 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.