Veeva CRM Administration or Engineer Pyramid Consulting, IncVeeva CRM Administration or EngineerBoston, MA$50–$55 / hourBy applying to our jobs you agree to receive calls, AI-generated calls, text messages, or emails from Pyramid Consulting, Inc. and its affiliates, and contracted partners. This is a 12+ Months Contract opportunity with long-term potential and is located in Boston, MA/Teaneck, NJ/San Francisco, CA (Hybrid) .
Senior Staff Accountant Mercy BioAnalytics IncSenior Staff AccountantWaltham, MARemote$94,000–$129,248 / yearThe Senior Staff Accountant plays a key role in ensuring accurate tracking of financial data, financial reporting, maintaining strong internal controls, and supporting the Company's accounting operations. Oversee all aspects of accounting, including maintenance of the general ledger, accounts payable, payroll, and month-end, quarter-end, and year-end financial statement consolidation and close process.
NewSenior Specialist, Biosamples Tango TherapeuticsSenior Specialist, BiosamplesBoston, MA$90,400–$135,600 / yearOversee shipment and receipt of clinical biosamples, document chain of custody throughout all stages of the clinical workflow and respond to issues as needed to ensure biosample custody is protected. Coordinate with internal and external stakeholders to manage the timely shipment of clinical samples, leveraging sample forecasts and inventory availability to support study milestones and laboratory testing needs.
NewManager, Commercial Supply Chain Operations Zenas BioPharmaManager, Commercial Supply Chain OperationsWaltham, MA$107,700–$134,636 / yearZenas' 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. Reporting to the Senior Director of Commercial Supply Chain Planning & Operations, the incumbent owns the tactical engine of commercial supply: finished goods planning and scheduling, inventory management and control, production schedule maintenance at CDMOs, and the coordination, shipping, and logistics required to keep inventory replenished and available.
NewSenior Specialist, Biosamples Tango Therapeutics IncSenior Specialist, BiosamplesBoston, MA$90,400–$135,600 / yearOversee shipment and receipt of clinical biosamples, document chain of custody throughout all stages of the clinical workflow and respond to issues as needed to ensure biosample custody is protected. Coordinate with internal and external stakeholders to manage the timely shipment of clinical samples, leveraging sample forecasts and inventory availability to support study milestones and laboratory testing needs.
Associate Director, Analytical Development & Quality Control Alpha-9 Oncology IncAssociate Director, Analytical Development & Quality ControlBoston, MAThe successful candidate will manage relationships with external manufacturing and testing partners while partnering closely with Quality, Regulatory, Technical Operations, and Program Leadership teams to support API development, CMC activities, and timely execution of clinical supply strategies. Alpha-9 Oncology is seeking a highly experienced and motivated Associate Director, Analytical Development & Quality Control, to provide technical and operational leadership for QC activities supporting our clinical-stage radiopharmaceutical programs.
Marketing Associate (Digital & Creative) Alloy Therapeutics IncMarketing Associate (Digital & Creative)Waltham, MA$80,000–$110,000 / yearThe company facilitates affordable, non-exclusive access to the entire drug discovery community from academic scientists, small and medium biotech, to the largest biopharma. For this role, the estimated range is $80,000 - $110,000, with the final offer based on factors like your experience, skills, and alignment with our needs.
MES Engineer Info Way Solutions LLCMES EngineerNorwood, MAThe MES Engineer will play a critical role in supporting the design, development, implementation and management of the Manufacturing Execution Solutions (MES) within the organization's Drug Product manufacturing area. Key Responsibilities: MES Support and Development: Assist in the design and configuration of Tempo MES solutions, including electronic batch records (eBRs), under the guidance of senior engineers.
Bioinformatics Senior Scientist-Biology Zealand Pharma A/SBioinformatics Senior Scientist-BiologyCambridge, MAAs Bioinformatics Sr Scientist II in Biology, the role provides bioinformatics support to the Global Biology research team across pipeline projects from discovery to clinic. Combining more than 25 years of peptide R&D expertise with a proprietary data platform that leverages advanced data-driven and AI/ML approaches, Zealand Pharma aims to lead a new era in obesity and metabolic health.
Scientific Change Management Consultant ZifoScientific Change Management ConsultantBoston, MARemote$110,000–$125,000The Scientific Change Management Consultant sits within the North American consulting group wherein key accountabilities include establishing and executing on change management strategies and deliverables, internal and external stakeholder management, driving project elucidation, and defining & driving project success in partnership with key collaborators. Serve as primary lead and point of contact to understand change needs within an engagement, propose solutions or forums, and execute agreed strategies and / or oversee business analysts or other project team members to successfully bring needed transformation to project.
Senior/Principal Scientist, MPN Biology, Translational Sciences PharmaEssentia U.S.A.Senior/Principal Scientist, MPN Biology, Translational SciencesBEDFORD, MAFull timeFounded in 2003 by a team of Taiwanese American executives and renowned scientists from U.S. biotechnology and pharmaceutical companies, today we are listed on the Taipei Exchange (TPEx: 6446) and are expanding our global presence with operations in the U.S., Japan, China and Korea, along with a world-class biologics production facility in Taichung. In this position, you will utilize your expertise in MPN stem cell biology, driver mutation signaling pathways, in vivo MPN mouse models and biomarker discovery to guide proof-of-concept (POC) studies, drug development and biomarker strategies, optimize dosing regimens, and ensure the safety and efficacy of investigational drugs.
Associate Scientific Strategy Consultant ZifoAssociate Scientific Strategy ConsultantBoston, MARemote$110,000–$125,000The Associate Scientific Strategy Consultant sits within the North American consulting group wherein key accountabilities include driving project elucidation, stakeholder management and defining & driving project success in partnership with internal and external stakeholders. Familiarity with scientific workflows (e.g., bioanalysis, compound management, medicinal chemistry)and key data concepts within the life sciences industry and relevance to operational activities and enabling decision-making.
Senior Manager, GMP Quality Operations Connexion Systems + EngineeringSenior Manager, GMP Quality OperationsRemote, USA, MARemote$85–$100 / hourA rapidly growing clinical-stage biopharmaceutical organization is seeking a Senior Manager, GMP Quality Operations to provide strategic and operational leadership across GMP Quality and Quality Systems initiatives. The ideal candidate will bring deep expertise in GMP quality operations within biologics or pharmaceutical manufacturing environments and demonstrate strong cross-functional leadership, operational excellence, and inspection-readiness experience.
NewLAB Vantage - Technical Architect Artech LLCLAB Vantage - Technical ArchitectBoston, MA$55–$58 / hourThe ideal candidate will have hands-on experience designing, configuring, and implementing LabVantage solutions, integrating laboratory instruments, and enabling seamless data exchange between analytical systems. This role requires strong technical architecture skills, expertise in Empower integration, SDMS, and instrument connectivity while ensuring data integrity, compliance, and laboratory automation best practices.
NewGMP Quality Assurance Consultant – Cell & Gene Therapy Stark Pharma Solutions IncGMP Quality Assurance Consultant – Cell & Gene TherapyBoston, MAWe are seeking an experienced GMP Quality Assurance Consultant to provide quality oversight and compliance support for Cell & Gene Therapy manufacturing operations, validation, laboratory, engineering, and capital projects in a GMP-regulated environment. Strong knowledge of GMP, QA, CAPA, Root Cause Analysis, Change Control, Risk Assessments, and aseptic processing.
Director, Commercial Strategy & New Product Planning MBX Biosciences IncDirector, Commercial Strategy & New Product PlanningCambridge, MAThe Company's pipeline includes canvuparatide (MBX 2109) for the treatment of chronic hypoparathyroidism preparing for Phase 3 development; and an obesity portfolio that includes MBX 4291 in Phase 1 development and MBX 5765 in preclinical development, as well as additional discovery candidates. This role is well suited for individuals coming from biopharmaceutical marketing, commercial strategy, business analytics, or leading life sciences consulting firms who are excited to build, influence decisions, and grow alongside an emerging organization.
Associate Director Clinical Supply Verastem IncAssociate Director Clinical SupplyNeedham, MA$175,000–$200,000 / yearThe Associate Director serves as the Global Clinical Supply representative on cross-functional program teams and partners closely with Clinical Operations, Program Management, CMC, Regulatory Affairs, Quality, and external partners to ensure uninterrupted clinical supply throughout the lifecycle of global clinical trials. This role supports all aspects of clinical supply management, including investigational medicinal product (IMP) and comparator sourcing, demand forecasting, packaging and labeling, distribution, inventory management, Interactive Response Technology (IRT), vendor oversight, and budget execution.
Sr Director, Commercial Strategy & Operations Syneos - Commercial - ProdSr Director, Commercial Strategy & OperationsBoston, MA$225,000–$245,000 / yearIn this role you will be accountable for the development, coordination, and measurement of strategic commercial initiatives, which impact the overall effectiveness of the organization, including incentive programs, POA execution,, operational excellence, training and monitoring,budget andexpense management, field force effectiveness (performance management and productivity analysis) as well as identifying key opportunities that will accelerate client objectives. Experience: Minimum of 10 years of relevant pharmaceutical or biotechnology industry experience, with sales leadership experience & direct experience in developing product strategy and executing product launches.
Associate Manager, Systems Engineer, IT Agios PharmaceuticalsAssociate Manager, Systems Engineer, ITCambridge, MA$94,025–$141,038 / yearDeliver excellent, customer-focused end-user support: work the service request and incident queue alongside the EUX team, resolve issues across the collaboration platform and general end-user computing, and grow into an escalation point for complex SharePoint, Teams, and Exchange Online issues as you develop expertise. This is a hands-on, customer-facing growth role at the intersection of platform administration and everyday end-user support - a strong opportunity for someone with solid IT support experience who is ready to develop deep specialization in our Microsoft 365 collaboration and productivity platform (SharePoint Online, Microsoft Teams, OneDrive, and Exchange Online).
Experienced Clinical Research Associate - Hematology/Oncology Medpace, Inc.Experienced Clinical Research Associate - Hematology/OncologyBoston, MassachusettsRemoteOn-site and virtual/remote monitoring activities with a risk-based monitoring approach (including centralized data review) through our integrated Clinical Trial Management System to identify site deviations/deficiencies and corrective/preventive actions to bring a site back into compliance and mitigate risks moving forward. When you join Medpace, you become part of an innovative team that brings cutting-edge therapies to market while building a meaningful and rewarding career focused on scientific excellence and improving patient outcomes around the world through continuous learning and cross-functional collaboration.