AIRx Director, Computational & AI Biologics Design Lead Takeda Pharmaceutical Co LtdAIRx Director, Computational & AI Biologics Design LeadBoston, MA$177,000–$278,080 / yearThis role drives in silico biologics design, applies generative AI and structure-informed methods to antibody and large-molecule programs, and connects Takeda's internal AI/ML platform capabilities to the day-to-day decisions of a fast-moving drug-hunting team. The actual base salary offered may depend on a variety of factors, including the qualifications of the individual applicant for the position, years of relevant experience, specific and unique skills, level of education attained, certifications or other professional licenses held, and the location in which the applicant lives and/or from which they will be performing the job.
Associate Director, Sales, Datapoints Small Molecule Business Ginkgo BioWorks IncAssociate Director, Sales, Datapoints Small Molecule BusinessBoston, MA3-7 years of experience in scientific roles (pharmacology, HTS, functional genomics, or chemical biology) and/or in commercial roles, BD, management consulting or strategic partnerships within life sciences. Ginkgo Datapoints is a newly established business unit within Ginkgo Bioworks, built to meet the growing demand for high-quality, large-scale biological datasets for AI-driven drug discovery.
Raven StealthCo - Scientist, Conjugation Chemistry RavenRaven StealthCo - Scientist, Conjugation ChemistryBoston, Massachusetts$120,000–$170,000 / yearKey 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.
Kearney Healthcare & Life Sciences Practice Manager Pharma Commercial Strategy A.T. Kearney IncKearney Healthcare & Life Sciences Practice Manager Pharma Commercial StrategyBoston, MA$212,000–$235,000 / yearWe are seeking experienced strategy consultants with deep expertise in commercial strategy within Life Sciences, particularly those with a traditional consulting background advising biopharma clients on growth, portfolio strategy, go-to-market strategy, and market access strategy. As a Manager, you will be an integral part of Kearney case teams, working closely with clients and colleagues to develop insights and deliver high-impact results.
Scientist II/Sr. Scientist I, Chemical Biology Antares TherapeuticsScientist II/Sr. Scientist I, Chemical BiologyBoston, MassachusettsAs a member of the team, you will be responsible for designing and executing proteomic screens to identify and validate novel therapeutic targets, elucidate mechanisms of inhibition, and enable biophysical small-molecule characterization through cycles of hit identification and SAR advancement. The actual salary offered will be based on a number of factors, including but not limited to the qualifications of the applicant, years of relevant experience, level of education attained, certifications or other professional licenses held, and if applicable, the location in which the applicant lives and/or from which they will be performing the job.
Research Science Analyst - Strategy and Corporate Finance - McKinsey Value Intelligence Platform McKinsey & Co IncResearch Science Analyst - Strategy and Corporate Finance - McKinsey Value Intelligence PlatformBoston, MAThis may include but is not limited to: experimental testing with new large language models (LLMs), structuring and implementing proof of concepts, enhancing existing functionality through new analytical approaches, and helping design end-to-end solutions alongside our engineers. You will be a part of the McKinsey Value Intelligence Platform, which is a cornerstone data and insights platform for the firm, supporting client delivery teams and clients with expert insights on companies and industries.
Medical Science Liaison / Senior Medical Science Liaison COVID/Virology New England Shionogi & Co LtdMedical Science Liaison / Senior Medical Science Liaison COVID/Virology New EnglandBoston, MA$175,000–$220,000 / yearPrevious MSL experience in the pharmaceutical/biopharmaceutical industry required with previous respiratory infectious disease experience preferred; experience in COVID-19 preferred OR, previous MSL experience in the pharmaceutical/biopharmaceutical industry preferred with previous respiratory infectious disease experience required. The Medical Science Liaison (MSL)/Senior Medical Science Liaison (Sr MSL) is a field-based representative of the Medical Affairs Organization that supports and represents Shionogi Inc and its products with, and to, key opinion leaders (KOLs), clinicians, institutions, and professional organizations.
Associate Scientist - Dissolution Thermo Fisher ScientificAssociate Scientist - DissolutionBoston, MassachusettsThrough this collaborative approach, our professionals bring their commitment to excellence, industry knowledge, and operational strength directly into customer environments, helping to enhance capabilities and advance the delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services.
Half (.5) Graduate Assistant - College of Humanities and Social Sciences, Deans Office Bridgewater State UniversityHalf (.5) Graduate Assistant - College of Humanities and Social Sciences, Deans OfficeBridgewater, MA5 GA position will provide a graduate student with valuable experience in recruitment for human-subject research, which is directly applicable to any social scientist career, especially regarding ethical research recruitment practices. 5 GA will also be asked to complete the national ethics training for working with human research participants (CITI training certificate) to provide a background in ethical recruitment of human participants.
Principal Scientist II - Pharmacology Novartis AGPrincipal Scientist II - PharmacologyCambridge, MA$126,000–$234,000 / yearResponsibilities:Design pre-clinical in vivo studies to explore novel hypotheses, screen candidate molecules, and establish proof-of-concept of new modalitiesDevelop in vivo CDX, PDX, and syngeneic models to evaluate anti-tumor activity, PK/PD relationships, relevant biomarkers, and key translational questionsManage associate-level scientistsCollaborate with cross-functional project teamsCritically analyze and present results within a multidisciplinary team environmentCareful adherence to animal protocols and proper documentation of data and methods in electronic laboratory notebookQualifications:PhD with 5-8 years of research experience as a postdoc or in the pharmaceutical/biotech industryDeep knowledge of antibody drug conjugatesExtensive experience working with CDX and PDX xenograft tumor models and/or syngeneic modelsExpertise in cell culture, PCR, ELISA, western blot, and flow cytometryStrong analytical, communication (written and verbal), and organizational skills, including a proficiency with PowerPoint and commonly used data analysis programs, such as Prism and ExcelNovartis Compensation and Benefit Summary: The salary for this position is expected to range between $126,000 and $234,000 per year. The successful candidate will join a dynamic, multi-disciplinary team and play a key role in the development and application of in vivo models for evaluating novel cancer therapies and advancing the early-stage drug discovery pipeline.
Life Sciences Corporate - Mid-Level Associate Attorney (Multi Office) Pernini Recruiting CompanyLife Sciences Corporate - Mid-Level Associate Attorney (Multi Office)Boston, MAThis is a unique opportunity to join one of the most highly-regarded Life Sciences Corporate practices in the country , working with industry pioneers and innovators shaping the future of healthcare and technology . 2-4 years of substantive experience handling a broad range of corporate and transactional matters , including public company work, registered equity offerings , SEC reporting , and mergers and acquisitions (M&A) transactions .
Manufacturing Science & Technology (MSAT) Engineer - Fermentation Process Development Kula Bio IncManufacturing Science & Technology (MSAT) Engineer - Fermentation Process DevelopmentNatick, MA$130,000–$145,000 / yearKula Bio is building a new platform for microbial bioinoculants that unlock nitrogen naturally - reducing reliance on synthetic fertilizers. We're at a critical stage of scale-out and looking for an MSAT Engineer to help transform our fermentation processes into robust, scalable production systems.
NewSenior Medical Laboratory Scientist, Blood Bank - Evening Shift Mass General BrighamSenior Medical Laboratory Scientist, Blood Bank - Evening ShiftBoston, MassachusettsNo Licenses and Credentials Medical Technologist (ASCP) [MLT, MT, MLA, Histologists] - American Society for Clinical Pathology Board of Certification (ASCP-BOC) required Experience lab experience 3-5 years required Knowledge, Skills and Abilities - The knowledge, both practical and theoretical, of tests and procedures necessary to review findings and advise and direct subordinates in action. The Medical Laboratory Scientist, Senior I, in their role as Technical Supervisor, Technical Consultant, or General Supervisor as defined by CLIA, may be delegated responsibility for the technical oversight of the laboratory, including day-to-day supervision of operations and personnel performing testing and reporting results.
Senior Medical Laboratory Scientist, Blood Bank - Day Shift Mass General BrighamSenior Medical Laboratory Scientist, Blood Bank - Day ShiftJamaica Plain, MassachusettsThe Medical Laboratory Scientist, Senior I, in their role as Technical Supervisor, Technical Consultant, or General Supervisor as defined by CLIA, may be delegated responsibility for the technical oversight of the laboratory, including day-to-day supervision of operations and personnel performing testing and reporting results. Under the general supervision of the Technical Director and Clinical Supervisors, the Senior Technologist I oversees assigned workstations, including Quality Control (QC) review, training, competency assessment of staff, and inventory management.
Senior Director, Pharmacovigilance (PV) Sciences Keros TherapeuticsSenior Director, Pharmacovigilance (PV) SciencesLexington, MA$245,000–$302,000 / yearLead and manage all medical safety and risk management related projects including planning, tracking and execution; provide vendor oversight for quality of ICSRs, similar case analysis, and aggregate safety reporting; lead initiatives from the scientific and PV regulation perspective such as inspection readiness, and launch readiness. The Senior Director, PV Sciences is responsible for safety surveillance and aggregate safety reports and works with PV physicians for signal/risk management for Keros products to support product safety and compliance with global drug safety regulations and functional procedures and provide vendor oversight to PV vendors.
Biology Lab Technician - Roxbury Community College Roxbury Community CollegeBiology Lab Technician - Roxbury Community CollegeBoston, MAThe Lab Technician performs laboratory and administrative work and is responsible for setting up laboratory experiments and related equipment/supplies for science labs; maintains inventory of laboratory equipment, materials and supplies; orders new/replacement mater. Location: Boston, MA Category: Full Time Staff Job Type: Full Time Posted On: Thu Apr 9 2026 Job Description: Title: Biology Lab Technician.
Medical Science Liaison (Anti-Infectives) – Midwest Azurity Pharmaceuticals - USMedical Science Liaison (Anti-Infectives) – MidwestWoburn, MARemoteMedical Affairs at Azurity Pharmaceuticals, a privately held company delivering innovative medicines for overlooked patients across 50+ countries, drives scientific and clinical initiatives with a portfolio of 40+ brands spanning 10 dosage forms and 9 therapeutic areas. MSLs are the field scientific experts in anti-infectives and treatment options within this therapeutic area and will support strategic Medical Affairs initiatives, evidence-generation activities, and field readiness efforts associated with the continued growth of the anti-infectives portfolio.
Medical Science Liaison (CORE) – Mid-Atlantic Azurity Pharmaceuticals - USMedical Science Liaison (CORE) – Mid-AtlanticWoburn, MARemoteMedical Affairs at Azurity Pharmaceuticals, a privately held company delivering innovative medicines for overlooked patients across 50+ countries, drives scientific and clinical initiatives with a portfolio of 40+ brands spanning 10 dosage forms and 9 therapeutic areas. As an industry leader in providing unique, accessible, and high-quality medications, Azurity leverages its integrated capabilities and vast partner network to continually expand its broad commercial product portfolio and robust late-stage pipeline.
Scientist - Solid State Characterization Thermo Fisher ScientificScientist - Solid State CharacterizationBoston, MassachusettsUse state-of-the-art technologies to support early and late stage pharmaceutical development with a variety of techniques including X-ray powder diffraction, differential scanning calorimetry, thermogravimetric analysis, dynamic light scattering, surface area measurement and SEM among others while onsite at a pharmaceutical client site. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services.
Distinguished Scientist, Safety Assessment Project Expert SanofiDistinguished Scientist, Safety Assessment Project ExpertCambridge, MA$178,500–$257,833.33 / yearThese activities entail formulating the nonclinical safety strategies, designing safety pharmacology and toxicology studies, authoring regulatory documents, being a member of an integrated Project Team, interacting with internal and external partners, and interacting with and responding to global regulatory agencies. Our Team: The candidate will be part of a dynamic interactive Preclinical Safety group that spans all aspects of the drug development value chain providing toxicology and safety pharmacology expertise as a member of global project teams.