Associate Director, Medical Training (Pipeline) Xenon PharmaceuticalsAssociate Director, Medical Training (Pipeline)Needham, MassachusettsOur Total Rewards program includes base salary, target bonus, and stock options, as well as a full range of benefits including medical, dental, vision, short-& long-term disability, accidental death & dismemberment, and life insurance programs, Employee Assistance Program, travel insurance, and retirement savings programs with company matching contributions. Training Module Development: Design and develop engaging training modules for different audiences and use-cases (field medical, sales, congress teams, cross-functional partners), incorporating adult learning principles, knowledge checks, and practical application exercises.
NewBusiness Development Lead - GLP-1 Waters CorporationBusiness Development Lead - GLP-1Milford, MassachusettsWorking in close partnership with regional commercial teams, field marketing, product management, R&D, applications, and scientific leaders, the successful candidate will help identify customer needs, evaluate market opportunities and manage the adoption of differentiated analytical solutions across the GLP-1 value chain - from discovery through to manufacturing and quality control. This is a unique opportunity to manage the development of our GLP-1 market strategy, identifying customer needs, informing cross-divisional product strategies and supporting commercial execution across our Liquid Chromatography, Mass Spectrometry, Software, and Chemistry businesses.
NewBusiness Development Lead GLP 1 Waters CorpBusiness Development Lead GLP 1Milford, MAWorking in close partnership with regional commercial teams, field marketing, product management, R&D, applications, and scientific leaders, the successful candidate will help identify customer needs, evaluate market opportunities and manage the adoption of differentiated analytical solutions across the GLP-1 value chain - from discovery through to manufacturing and quality control. This is a unique opportunity to manage the development of our GLP-1 market strategy, identifying customer needs, informing cross-divisional product strategies and supporting commercial execution across our Liquid Chromatography, Mass Spectrometry, Software, and Chemistry businesses.
NewSenior Marketing Events Manager Azenta IncSenior Marketing Events ManagerBurlington, MA$108,000–$135,000 / yearWe are a market leader in automated bio sample management solutions and genomic services across areas such as drug development, clinical and advanced cell therapies for the industry's top pharmaceutical, biotech, academic and healthcare institutions globally. We provide unparalleled capabilities with our lab analysis, sample management and storage services, informatics software, and consumables, with the largest installed base managing millions of samples globally.
Senior Solution Architect DP Technology Co LtdSenior Solution ArchitectBoston, MA3+ years of experience in drug discovery, computational chemistry, AI-driven research platforms, or related scientific technology roles • Master's or PhD degree in chemistry, biology, pharmaceutical sciences, computational science, or a related field • Strong ability to translate complex scientific and technical concepts into structured, client-ready solutions • Experience engaging directly with external scientific and technical stakeholders • Excellent communication skills, with confidence presenting to both technical experts and senior decision-makers. • Design customized drug discovery and Agentic AI solution architectures tailored to the scientific objectives, constraints, and maturity of biotech and pharma partners • Translate customer scientific challenges into structured solution frameworks, including: • Platform configurations • Workflow designs • Scope definitions and success criteria • Balance scientific rigor, technical feasibility, and commercial practicality when shaping proposed solutions • Serve as the primary owner of the solution narrative, ensuring consistency across technical, scientific, and business dimensions.
Business Development Manager - truCOLLECT PerkinElmer US LLCBusiness Development Manager - truCOLLECTWoburn, MA$150,000–$175,000 / yearUsing proprietary technologies including focused acoustic energy, Covaris' tools achieve highly accurate and reproducible results with the goal of empowering customers to make new discoveries, develop new assays and improve bioanalytical results. This role is responsible for identifying strategic partnerships, expanding market penetration, and accelerating revenue growth across clinical research organizations (CROs), biopharma, diagnostics labs, digital health platforms, and healthcare systems.
Senior Director, Launch Excellence Swedish Orphan Biovitrum ABSenior Director, Launch ExcellenceBoston, MA$215,000–$270,000 / yearThe Senior Director, Launch Excellence will provide strategic leadership and operational oversight to ensure the successful, on-time, and high-quality launch of Sobi''s launches in future pipeline products, including two core upcoming launches across the North America region. In partnership with an Asset Launch Lead, lead a high-performing, cross-functional launch team including representatives from Marketing, Sales, Medical Affairs, Market Access, Customer Experience, Insights and Operations, Supply Chain, and Regulatory Affairs.
Event Manager ITA GroupEvent ManagerBoston, MAThe Event Manager - Internal Meetings coordinates the operation of pharmaceutical meeting including Sales Meeting, Regional POAs, National POAs, Launches, Leadership Meetings and Incentives for specific Life Sciences clients, and serves as a leader for the internal team. Ability to listen, understand and respond to external and internal customers' needs in a timely manner; customer service experience in a service-related industry preferred.
Sr. Medical Writer Integrated Resources, IncSr. Medical WriterMansfield, MassachusettsFull timeThis position will meet and communicate regularly with Clinical Affairs, PACE, R&D, marketing, Sales, KOL's and others as necessary to build and collaborateQualificationsSpecial Notes:100% remote work is possible, on site is preferredPHD with 5+ years of experience or Nurses with 10+ years of experience is requiredThe Medical Writer has to review the post market surveillance data, has to create a demonstration of safety reportsExtensive experience with Clinical Evaluation Report is required, person has to be able analyze complex scientific informationPost Marker Surveillance experience is requiredGood understanding of risk management and hands on experience with risk management documentation is requiredAdditional InformationKind Regards,Sabanaaz ShaikhClinical RecruiterIntegrated Resources, Inc. abstracts, manuscripts, presentationsRequires a strategic understanding of the therapeutic areas, business and study objectives as well as statistical dataIndependently, critically writes and edits scientifically complex documents for substantial intellectual contentReviews and provides input on the data being considered for publication to ensure alignment with current medical issues and corporate goalsExpert knowledge of clinical research, device/drug development processes, regulatory requirements, and good clinical practicesAbility to understand and interpret statistical results of clinical studies; ability to summarize complex results and present them in a clear, concise, and scientifically accurate manner to a wide range of audiencesNon-essential functions:1.
Senior Manager- Knowledge Management for Clinical Affairs Integrated Resources, IncSenior Manager- Knowledge Management for Clinical AffairsCambridge, MassachusettsContractorJob DescriptionJob Title: Senior Manager – Knowledge Management for Medical AffairsDuration: 14+ MonthsLocation: Cambridge, MAResponsibilities:Gathering end user requirements from key stakeholders and review of technical specifications for information governance in partnership with IT, maintaining of critical functionality of the CRM platform to ensure uninterrupted access by HCPs to company product information;Creation and maintenance of all metrics and analytic tools necessary for supporting GMA decision making and maintenance of the content management system used by Worldwide Medical. Project management expertise with focus on driving for results and sense of urgencyMinimum of 7-10 years clinical data systems experience working in the biotechnology or pharmaceutical industryExperience applying best practices in application development to the clinical trial environment, including requirements definition and QC plansAware of current global regulatory guidelines relevant to Clinical Data Management, as well as related Pharma Development SOPs, guidelines and Best Practices.
Medical Science Liaison, Lung/GU Oncology (MA, NH, VT, ME) Bristol-Myers Squibb CoMedical Science Liaison, Lung/GU Oncology (MA, NH, VT, ME)Boston, MARemote$168,220–$203,837 / yearAs this position requires the operation of a Company-provided vehicle, offers of employment are contingent upon the candidate meeting the requirements of "Qualified Driver," as determined by the Company in its sole discretion, including but not limited to the following: 1) at least 21 years of age; 2) a driver's license in good standing issued by your state of residence; and, 3) a driving risk level deemed acceptable by the Company. The primary role of the Medical Science Liaison (MSL) is to engage in meaningful peer-to-peer scientific dialogue with healthcare system leaders such as Regional Thought Leaders (RTLs), National Thought Leaders, and Healthcare Professional (HCPs) within a defined geography to translate science into patient care.
NewMedical Science Liaison, Lung/Gu Oncology (Ma, NH, VT, ME) Bristol Myers SquibbMedical Science Liaison, Lung/Gu Oncology (Ma, NH, VT, ME)Boston, MARemote$168,220–$203,837 / yearAs this position requires the operation of a Company-provided vehicle, offers of employment are contingent upon the candidate meeting the requirements of "Qualified Driver," as determined by the Company in its sole discretion, including but not limited to the following: 1) at least 21 years of age; 2) a driver's license in good standing issued by your state of residence; and, 3) a driving risk level deemed acceptable by the Company. The primary role of the Medical Science Liaison (MSL) is to engage in meaningful peer-to-peer scientific dialogue with healthcare system leaders such as Regional Thought Leaders (RTLs), National Thought Leaders, and Healthcare Professional (HCPs) within a defined geography to translate science into patient care.
New["Pain Territory Account Manager - Fort Smith & Fayetteville Arkansas","Pain Territory Account Manager - Fort Smith & Fayetteville Arkansas"] Vertex Pharmaceuticals["Pain Territory Account Manager - Fort Smith & Fayetteville Arkansas","Pain Territory Account Manager - Fort Smith & Fayetteville Arkansas"]Boston$133,600–$200,400 / yearThe Pain Territory Account Manager (PTAM) is responsible for establishing and maintaining relationships with key institutional decision makers and affiliated Health Care Professionals (HCPs) to promote the safe and effective use of JOURNAVX, a novel selective inhibitor ofNaVl.8 in acute pain. Collaborates compliantly with other field team members (e.g., Territory Business Managers, field medical, HEOR, IDN and Payer Account teams) and headquarter colleagues to create aligned business plans, focus on strategic drivers, share best practices, and inform initiatives.
Principal, Commercial Life Sciences Solutions DatavantPrincipal, Commercial Life Sciences SolutionsBoston, MA$193,000–$242,000 / yearStay current on trends shaping commercial pharma data strategy, including real-world data adoption, healthcare media networks, clean rooms, first-party data strategy, privacy-preserving collaboration, tokenization, AI-enabled analytics, and the evolving life sciences data ecosystem. This role is highly customer-facing and requires deep understanding of how pharmaceutical organizations use data to support therapy adoption, launch planning, market access, patient and provider insights, medical affairs, HEOR, omnichannel engagement, healthcare marketing, and real-world evidence generation.
Director, US Advertising and Promotional Compliance AstraZeneca PlcDirector, US Advertising and Promotional ComplianceBoston, MA$193,281–$289,922 / yearWe operate with the focus of a nimble biotech and the reach of a global biopharma, bringing unexpected teams together to spark bold thinking that turns complex biology into meaningful patient impact. The Director will also engage business partners for strategic planning on issues pertaining to product promotion and will participate in developing processes and procedures relevant to the creation, review and approval of promotional material.
Global Product Leader, Late CVRM - Weight Management AstraZeneca PlcGlobal Product Leader, Late CVRM - Weight ManagementCambridge, MA$251,610.40–$377,415.60 / yearInnovate and explore novel methods to accelerate dyslipidemia FDC development, leveraging new opportunities and prioritization within the franchise to maximize its value Risk and Opportunity Management: Identify, assess, and manage risks, opportunities, and strategic issues, escalating to the franchise head as necessary. As a Global Product Leader (GPL) in the weight management franchise, you will play a pivotal leadership role with accountabilities critical to delivering AstraZeneca's business objectives and portfolio value targets.
NewDirector, Life Sciences Iterative Scopes IncDirector, Life SciencesBoston, MA$180,000–$250,000 / yearThis highly visible, external-facing role will be responsible for identifying, developing, and expanding partnerships with biopharmaceutical and biotechnology sponsors, helping bring innovative therapies to patients through cutting-edge clinical research. We built a leading performance-driven network of 100+ sites across the US, Europe, India, and Australia, conducting research directly in the communities where care is delivered across gastrointestinal, hepatology, obesity, and cardiology.
Director, Life Sciences Business Development Iterative Scopes IncDirector, Life Sciences Business DevelopmentBoston, MA$180,000–$250,000 / yearThis highly visible, external-facing role will be responsible for identifying, developing, and expanding partnerships with biopharmaceutical and biotechnology sponsors, helping bring innovative therapies to patients through cutting-edge clinical research. We built a leading performance-driven network of 100+ sites across the US, Europe, India, and Australia, conducting research directly in the communities where care is delivered across gastrointestinal, hepatology, obesity, and cardiology.
Vice President, Compliance Beam TherapeuticsVice President, ComplianceCambridge, MA$310,000–$400,000 / yearDemonstrated knowledge and understanding of the legal and regulatory framework affecting the pharmaceutical industry including sales and marketing, OIG and other industry guidance documents, regulations on the promotion of marketed products, clinical trial regulations, patient privacy and issues arising under the False Claims Act, anti-bribery/anti-corruption laws, and other related laws. Provide proactive strategic advice to the business to help drive commercial success and ensure compliance with applicable laws and company policies, including federal and state anti-kickback and false claims laws; U.S. and other country anticorruption laws; the federal Food, Drug and Cosmetic Act; and federal and state transparency laws.
Customer Service Specialist Temporary Part Time BiofronteraCustomer Service Specialist Temporary Part TimeWoburn, MA$25–$35 / hourIn this role, the Specialist will handle complex service interactions—including order fulfillment, shipment coordination, and issue resolution—while also developing new business leads, maintaining customer relationships, and supporting sales efforts. This hybrid position combines responsibilities from both customer service and inside sales, ensuring seamless coordination between order processing, customer support, and commercial initiatives/support.