Director, Global Clinical Physician (Cardiovascular) Bristol-Myers Squibb CoDirector, Global Clinical Physician (Cardiovascular)MA$308,700–$374,075 / yearAdvanced planning/project management skills (develop realistic, effective medium-range plans across clinical development programs and deal timelines, managing competing priorities across multiple concurrent deals). Based on eligibility*, additional time off for employees may include unlimited paid sick time, up to 2 paid volunteer days per year, summer hours flexibility, leaves of absence for medical, personal, parental, caregiver, bereavement, and military needs and an annual Global Shutdown between Christmas and New Years Day.
NewMedical Science Liason (MSL) - Podiatry, Men's Health and Ortho (Northeast) Mallinckrodt LLCMedical Science Liason (MSL) - Podiatry, Men's Health and Ortho (Northeast)Boston, MARemote$157,000–$186,000 / yearThis is a field-based Medical Affairs position requiring a strong scientific background (technical or clinical experience) as the MSL will be a credible source of clinical/scientific data as well as technical/practical education to practicing clinicians, key opinion leaders (KOL), professional societies, and payers. A Medical Science Liaison (MSL) will serve as a liaison to the medical/scientific community and will be responsible for establishing, developing and maintaining relationships with key stakeholders within the geographic and therapeutic area of coverage.
Senior Director, Discovery & Translational De Solid Biosciences IncSenior Director, Discovery & Translational DeMA$260,000–$305,000 / yearSolid Biosciences is a precision genetic medicine company focused on advancing a portfolio of gene therapy candidates targeting rare neuromuscular and cardiac diseases, including Duchenne muscular dystrophy (Duchenne), Friedreich's ataxia (FA), catecholaminergic polymorphic ventricular tachycardia (CPVT), TNNT2-mediated dilated cardiomyopathy, BAG3-mediated dilated cardiomyopathy, and additional fatal, genetic cardiac diseases. The successful candidate will lead a team responsible for multiple pipeline programs, including Friedreich's ataxia, CPVT, emerging genetic cardiomyopathy programs, additional new pipeline opportunities, and clinical assay oversight across advancing programs.
Senior Director, Global Head of Clinical Operations Olympus CorpSenior Director, Global Head of Clinical OperationsWestborough, MAThe Sr Director, Global Head of Clinical Operations reports directly to the Global Head of Clinical Research and collaborates closely with the MSA leadership team to provide strategic leadership and direction for the clinical operations team including the oversight of all aspects of clinical studies in support of clinical evidence generation strategies across global business unit portfolios. The individual is a critical member of Clinical Affairs leadership team and collaborates with cross-functional teams including internal and external business stakeholders within MSA, across the global business units, and within the broader Olympus organization, as appropriate.
Sr. Supplier Quality Engineer - Metals (Onsite - Acton, MA) Insulet CorpSr. Supplier Quality Engineer - Metals (Onsite - Acton, MA)Acton, MA$87,100–$130,600 / yearManagement, Manufacturing Operations, Production Operations, Supplier Development Engineering, Design Engineering, Information Technology, Engineering, Procurement, New Business Development and Regulatory Affairs) as well as suppliers, contractors, and other external parties on issues related to supplier quality, quality management systems, materials, product support and external and internal audit support. The Supplier Quality Engineer works closely with suppliers and internal teams to ensure products meet quality and regulatory requirements, drive supplier performance improvements, investigate and resolve quality issues, and support sourcing and manufacturing initiatives.
Product Quality Assurance Engineer ZOLL MedicalProduct Quality Assurance EngineerChelmsford, MassachusettsRemote$82,400–$90,000 / yearThis role partners with Engineering, Manufacturing, Regulatory, and Post-Market teams to support investigations, analyze product performance, and contribute to activities that improve product reliability, patient safety, and compliance for medical devices. Job Summary The Product Quality Assurance Engineer supports product quality throughout the product lifecycle, with a focus on complaint investigations, risk management support, and product quality monitoring.
Senior Director, Quality Assurance, Commercial Xenon PharmaceuticalsSenior Director, Quality Assurance, CommercialNeedham, 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. We are seeking a Senior Director, Quality Assurance, Commercial as an integral leader within the Quality GMP team as well as a key member of highly collaborative R&D Operations group comprised of Program Management, CMC, Regulatory Affairs, Supply Chain and Quality functions.
NewDirector/Senior Director, Nonclinical Safety Toxicology Nimbus Therapeutics LLCDirector/Senior Director, Nonclinical Safety ToxicologyBoston, MA$225,000–$285,000 / yearManage nonclinical safety studies conducted by CROs with efficient governance including contract execution, authorization of study amendments, schedule and budget variance management, progress reporting to stakeholders, review of data and draft study reports, completion of contract milestones, study close-out and alignment of nonclinical safety evaluations with drug development efforts and priorities. Collaborate with CMC, Program & Portfolio Management, Clinical, Medical, and Regulatory Affairs to develop program-specific strategies for appropriate data generation in support of development candidate nomination, IND/CTA filing, and clinical development of new small molecule drug entities.
(Senior-) Director Head of Medical Review (Pharmacovigilance) BioNTech SE(Senior-) Director Head of Medical Review (Pharmacovigilance)Cambridge, MAYour benefits and remuneration: If the position is filled in the US, the Expected Pay Range for Director is $168,100/year to $268,700/year and Senior Director is $198,900/year to $318,300/year + benefits, annual bonus & equity (bonus and equity is variable and dependent on company and individual performance). Oversee high-quality medical assessments of ICSRs, focusing on critical cases such as SUSARs, immune-mediated events, and potential Drug-Induced Liver Injury (pDILI).
Executive Medical Director, Clinical Development- Immunology Vertex PharmaceuticalsExecutive Medical Director, Clinical Development- ImmunologyBoston, MassachusettsAs Executive Medical Director, Clinical Development , you will serve as Vertex's primary physician voice on the povetacicept franchise in immunology while contributing your scientific perspective to how Vertex thinks about immunology more broadly about which programs to advance, which mechanisms to pursue, and how to position Vertex as a credible, durable force in a field that is moving fast. We are seeking a physician-scientist with a comprehensive understanding of molecular pathways as drivers of inflammatory and autoimmune diseases across a range of organs — and of the investigative treatment landscape targeting those pathways — to help shape Vertex's immunology portfolio beyond existing programs.
NewExecutive Medical Director- Nephrology Vertex PharmaceuticalsExecutive Medical Director- NephrologyBoston, Massachusetts$320,000–$480,000 / yearThe Executive Medical Director, Clinical Development will provide high-level input on clinical development strategies to povetacicept renal programs, in conjunction with other relevant functional area leaders in Medical Affairs, Regulatory, Global Patient Safety, Clinical Operations, Exploratory Development, Commercial, Pharmaceutical Development, Research, Business Development, and Marketing. At 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.
Medical Science Liaison, Hematology - Northeast Jazz Pharmaceuticals PlcMedical Science Liaison, Hematology - NortheastBoston, MARemote$160,000–$240,000 / yearThe successful candidate may also be eligible for a discretionary annual cash bonus or incentive compensation (depending on the role), in accordance with the terms of the Company's Global Cash Bonus Plan or Incentive Compensation Plan, as well as discretionary equity grants in accordance with Jazz's Long Term Equity Incentive Plan. Consistently acts to enhance Jazz Pharmaceuticals' image as an advocate of medical advancement by using knowledge of product, disease state and pipeline products to engage healthcare providers in meaningful scientific exchange of information.
NewSenior Scientist I, Quality Control Candel Therapeutics Inc.Senior Scientist I, Quality ControlNeedham, MA$155,000–$160,000 / yearThis position collaborates with external manufacturing and tech transfer and is focused on Adenovirus and Herpesvirus vectors, associated cell-based potency assays, as well as performing training of new technical staff and troubleshooting and validation of new and established assays. The Senior Scientist I, Quality Control works with various cell lines, performs analytical methods, trends quality attributes, and suitability of product lines for continued use.
Global Managed Access Manager LancesoftGlobal Managed Access ManagerWaltham, MA$1Job Description: Work with internal stakeholders to provide operational leadership for CLIENT oncology expanded access/compassionate programs including plans and strategies for footprint, drug supply, regulatory coordination, physician oversight, vendor set up and management, safety reporting, and other related activities accordance with CLIENT Policies and SOPs. Establish strong relationships with all stakeholders, including Global Medical Affairs colleagues, Supply team, LOCs, physicians, program managers, regulatory and safety teams as well as external vendors.
Operational Excellence Lead I (Pharmd) Replimune Group, Inc.Operational Excellence Lead I (Pharmd)Woburn, MA$170,000–$218,000 / yearWorking as a member of the Operational Launch Excellence Team, this individual will work in close collaboration with field sales and other staff to partner with treatment centers to assess operational readiness, facilitate Operational Workflow Meetings, identify implementation barriers, and optimize workflows to ensure successful adoption of RP1. The successful candidate will collaborate closely with multi-disciplinary care teams including but not limited to, medical oncology, pharmacy, nursing, interventional radiology, and practice leadership to help sites across the US operationalize RP1 and deliver positive treatment experiences.
Sr. Product Marketing Manager - Consumer Insulet CorpSr. Product Marketing Manager - ConsumerActon, MA$154,400–$231,575 / yearInsulet's latest innovation, the Omnipod 5 Automated Insulin Delivery System, is a tubeless automated insulin delivery system, integrated with a continuous glucose monitor to manage blood sugar with no multiple daily injections, zero finger sticks, and is fully controlled by a compatible personal smartphone. Insulet is proud to be recognized as a 2022 Top Workplace USA; awarded Top Workplaces Cultural Excellence Award for remote work; recognized as a Great Place to Work in four international locations in 2023; and ranked as one of America's most responsible companies by Newsweek.
Sr Manager, Fp&A - Global Operations (Boston Based) Haemonetics Corp.Sr Manager, Fp&A - Global Operations (Boston Based)Boston, MA$124,300–$211,700 / yearThe successful candidate will bring a passion and proven capabilities in: (1) designing and managing financial reporting, planning and analytics processes, (2) developing trusted business partner relationships ideally within a global manufacturing & supply chain function, and (3) partnering with technical teams to translate complex financial reporting and analytics requirements into technology requirements for efficient solution delivery. Reporting to the VP, Global Operations Finance, the Senior Manager will act as the leader and central point of contact for all core financial planning and analysis processes and communications supporting the COO-lead organizations (Global Manufacturing & Supply Chain, R&D, Quality and Regulatory Affairs).
Principal Software Applications Engineer Onsite in Burlington MA Glaukos CorpPrincipal Software Applications Engineer Onsite in Burlington MABurlington, MAReporting to the Director of Software Development, the Principal Software Development Engineer works side-by-side with software, electrical, mechanical engineers, and scientists to design and create software code within our products to achieve design goals. Founded in 1998, Glaukos Corporation is an ophthalmic pharmaceutical and medical technology company focused on developing and commercializing novel therapies for the treatment of glaucoma, corneal disorders, and retinal diseases.
Sr Manager, FP&A - Global Operations (Boston based) Haemonetics CorpSr Manager, FP&A - Global Operations (Boston based)Boston, MA$124,300–$211,700 / yearThe successful candidate will bring a passion and proven capabilities in: (1) designing and managing financial reporting, planning and analytics processes, (2) developing trusted business partner relationships ideally within a global manufacturing & supply chain function, and (3) partnering with technical teams to translate complex financial reporting and analytics requirements into technology requirements for efficient solution delivery. Reporting to the VP, Global Operations Finance, the Senior Manager will act as the leader and central point of contact for all core financial planning and analysis processes and communications supporting the COO-lead organizations (Global Manufacturing & Supply Chain, R&D, Quality and Regulatory Affairs).
Vice President, Head Of Life Cycle Management AlkermesVice President, Head Of Life Cycle ManagementWaltham, MA$360,000–$420,000 / yearThis individual will need to effectively collaborate and communicate with colleagues within Medical Affairs and key cross-functional partners (e.g., Commercial, Clinical Development, Clinical Operations, Regulatory Affairs, Safety, Biostatistics, Program Management, Government Affairs, Business Development), and frequently represent the function to senior management and the company to healthcare professionals. In 2024 and 2025, we were certified as a Great Place to Work in the U.S. and named one of Massachusetts' Top Places to Work by the Boston Globe, a Best Place to Work in Greater Cincinnati by the Cincinnati Business Courier and recognized as a Best Place to Work in BioPharma by Fortune Magazine.