Director, HEOR – Orexin Franchise Centessa Pharmaceuticals, LLCDirector, HEOR – Orexin FranchiseBoston, MA$180,000–$260,000 / yearReporting to the Executive Director, HEOR, the, you will partner extensively with Medical Affairs, Clinical Development, Market Access, Commercial, Legal, Regulatory, and external research partners to translate strategic objectives into actionable, well-governed research plans throughout the product lifecycle — from early pipeline evidence generation and launch readiness through post-launch value demonstration. Lead and manage HEOR studies, including retrospective and prospective observational studies, database analyses (claims, EHR, registries), and innovative designs such as external control arms to contextualize single-arm trial data.
Director, Regulatory Affairs Repertoire Immune MedicinesDirector, Regulatory AffairsWatertown, MA$210,000–$245,000 / yearThe DECODE platform has been validated through four strategic partnerships with leading pharmaceutical companies—Bristol Myers Squibb, Genentech, Eli Lilly, and Pfizer—representing over $4.5 billion in disclosed total deal value and $185 million in upfront payments received to date. The Director will own global regulatory strategy and execution across Phase 1 and Phase 2 development in the U.S., EU, and UK, partnering closely with Clinical Development, Clinical Operations, CMC, Quality, and external regulatory partners.
Director, External Quality Control & Stability Centessa Pharmaceuticals, LLCDirector, External Quality Control & StabilityBoston, MA$150,000–$210,000 / yearCentessa Pharmaceuticals, a wholly owned subsidiary of Eli Lilly and Company, is a clinical-stage company developing orexin receptor 2 (OX2R) agonists as a new class of medicines for the treatment of narcolepsy and potentially other sleep-wake disorders. The Director, External Quality Control & Stability will provide leadership and oversight for analytical testing, stability programs, specification management, and quality control activities supporting clinical and commercial development.
Senior Director, National Accounts Disc Medicine IncSenior Director, National Accountsmassachusetts, MA$261,000–$319,000 / yearPOSITION OVERVIEW: Reporting to the Vice President, Market Access, the National Account Director is responsible for executing market access strategies to ensure that national/regional, payers, PBMs, and GPO customers provide appropriate patient access to Disc's therapies. The Director will lead all activities with assigned national/regional commercial and government payers, managing relationships with senior managed care executives, and leveraging internal subject matter experts to communicate the value of Disc's therapies.
Director, Contracts Counsel MBX BiosciencesDirector, Contracts CounselBurlington, MAAdditional more detailed summary of responsibilities include: Draft, review, and negotiate a wide variety of agreements, including but not limited to: clinical trial agreements (CTAs), master service agreements (MSAs) and statements of work with CROs and clinical sites, confidentiality/non-disclosure agreements, material transfer agreements (MTAs), consulting and advisory agreements, manufacturing and supply agreements, quality agreements, licensing and collaboration agreements, and vendor/procurement contracts. Our pipeline includes canvuparatide (MBX 2109) for the treatment of chronic hypoparathyroidism, currently preparing for Phase 3 development, and a growing obesity portfolio that includes MBX 4291 in Phase 1 development, MBX 5765, a next-generation amycretin prodrug designed for once-monthly-dosing, as well as MBX 6180, a GLP/GIP/GCGR triple agonist prodrug for once monthly dosing; all of which optimize our PEP platform.
Director of Marketing Who We Are CYTENADirector of MarketingBoston, MassachusettsOur award-winning technologies are used by leading academic institutions, biotechnology companies, and pharmaceutical organizations worldwide to automate workflows across applications including cell line development, single-cell analysis, high-throughput screening, and drug discovery. The ideal candidate combines strategic thinking with operational excellence and has a proven track record of driving growth in life science, laboratory technology, biotechnology, medical device, or related B2B environments.
Director of Outpatient Services $5k Sign On Bonus Haverhill Behavioral HealthDirector of Outpatient Services $5k Sign On BonusHaverhill, Massachusetts$105,000–$125,000 / yearThe Director of Outpatient Services is responsible for leading the day-to-day operations and long-term success of the facility’s partial hospitalization programs (PHP) and intensive outpatient programs (IOP). The Director will serve as a clinical leader, performance coach, and community advocate, ensuring a seamless transition for patients stepping down from inpatient care and patients stepping up from community-based care.
NewSenior Director of Marketing (Consumer) Cascadia Search GroupSenior Director of Marketing (Consumer)Boston, MA$236,000–$324,500 / yearSuccess requires balancing short-term revenue growth for Vyvgart Hytrulo with long-term CIDP-MMN portfolio strategy, shaping the market to expand category demand, and building a cohesive enterprise narrative that maximizes total franchise growth. argenx is preparing for multi-dimensional expansion to reach more patients through a rich pipeline of differentiated assets, led by VYVGART (a first-in-class neonatal Fc receptor blocker approved for gMG, with potential across dozens of severe autoimmune diseases).
Associate Director, Patient Services Operations and Marketing Kiniksa Pharmaceuticals CorpAssociate Director, Patient Services Operations and MarketingLexington, MA$160,000–$175,000 / yearReporting to the Vice President of Patient Services, the Associate Director Patient Services Operations and Marketing is responsible for the ongoing management, optimization, and strategic execution of Patient Services operations, program vendors, and marketing assets. This role is a key operational partner between Patient Services and cross-functional stakeholders, ensuring Patient Services programs are delivered efficiently, consistently, and in alignment, while maintaining a high-quality patient and provider experience.
Associate Director, R&D Quality Engineering Boston Dynamics IncAssociate Director, R&D Quality EngineeringWaltham, MA$155,000–$195,000 / yearThe Associate Director, R&D Quality Engineering is a senior leadership role responsible for the quality engineering function across Prototype Operations - spanning prototype builds, low-volume production, supplier quality, and the failure investigation discipline that turns hardware problems into design and process improvements. Define and execute a quality strategy fit for prototype-to-production reality: right-sized controls that scale with build rate and design maturity, applied deliberately rather than inherited from mass-production dogma.
Sr. Director, Regulatory Strategy Genetix Biotherapeutics IncSr. Director, Regulatory StrategySomerville, MA$265,000–$331,000 / yearThe successful candidate must have strong written and oral communication skills and have experience writing regulatory briefing documents, leading meetings with health authorities, and partnering with regulatory agencies to advance complex therapies (experience with cell or gene therapies is preferred.) An additional key responsibility will be working to develop and execute the regulatory roadmap to support future European Union submissions for existing products, including regulatory gap assessments, EU engagement strategy, pediatric planning, and preparation for Marketing Authorization Applications (MAAs).
Director/Sr. Director, US Regulatory Advertising and Promotion Genetix Biotherapeutics IncDirector/Sr. Director, US Regulatory Advertising and PromotionSomerville, MA$185,000–$285,000 / yearThe Director serves as a key regulatory partner to Medical Affairs, Commercial, Marketing, and Legal, and plays a central role in promotional material review in a highly regulated environment, for cell and gene therapy products. Actual base salary pay will be based on several factors, including but not limited to experience, skills, relevant education/qualifications, external market, internal equity, and other job-related factors permitted by law.
Sr. Director, Quality Operations Genetix Biotherapeutics IncSr. Director, Quality OperationsSomerville, MA$250,000–$302,000 / yearThe Senior Director, Quality Operations is a senior quality leader responsible for providing strategic and operational leadership for commercial Quality Operations, including external manufacturing and testing oversight, lot disposition, quality governance, and patient-specific product controls across clinical and commercial-stage supply. This role partners closely with Manufacturing, Technical Operations, Supply Chain, Regulatory Affairs, Medical, Patient Operations, and Commercial teams to ensure uninterrupted and compliant patient supply, timely quality decisions, and sustained inspection readiness as the organization scales.
Senior Director, Device Engineering Scholar Rock Holding CorpSenior Director, Device EngineeringCambridge, MA$245,000–$325,000 / yearYou will lead key device development activities, including design controls, drug-device integration, assembly process development, characterization/validation, device risk analysis, design history file (DHF) management, verification and validation, design transfer and human factors engineering. This is a hands-on technical role, in which you will help shape and execute device engineering strategy for biologic assets, including the development of subcutaneous presentations using prefilled syringe (PFS) and autoinjector technologies, as well as drug delivery solutions for future pipeline assets.
NewResidence Director I (4085) Seven Hills Foundation IncResidence Director I (4085)Beverly, MA$3–$5 / hourThe primary objective of the Residence Director is to ensure responsive, effective residential supports to individuals with disabilities and to lead the staff team in creating an atmosphere that places individual respect, dignity and empowerment above all else. This position is responsible for the day-to-day operations of assigned residence with the goal of maintaining and enhancing the quality of program services offered.
Director of Product, Life Sciences (Chemistry) Lila SciencesDirector of Product, Life Sciences (Chemistry)Cambridge, Massachusetts7+ years of product leadership (PM, Group PM, Product Lead) building and launching complex technical products: therapeutic platforms, scientific software or hardware, simulation and modeling platforms, data products, or ML-enabled systems. You will be deeply customer-facing, serving as a trusted technical and product voice with prospects and partners, shaping proposals, driving commercial conversations, and closing deals that bring Lila's therapeutics platform to market.
Director, IT Business Partner Commercial ReplimuneDirector, IT Business Partner CommercialWoburn, MassachusettsThe RPx platform is designed to have a unique dual local and systemic activity consisting of direct selective virus-mediated killing of the tumor resulting in the release of tumor derived antigens and altering of the tumor microenvironment to ignite a strong and durable systemic response. · Oversee the support and integration of various marketing tools and platforms with the CRM (Salesforce/Veeva/TraceLink/Antaras) system to enhance marketing automation and customer interaction and manage third party support providers.
Associate Director or Director, Clinical Scientist Kymera Therapeutics IncAssociate Director or Director, Clinical ScientistWatertown, MA$160,000–$275,000 / yearHaving 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. Skills and experience you'll bring: Bachelor's or advanced degree (MSc, PharmD, PhD) in Life Sciences or related field and 8+ years in pharmaceutical clinical drug development, with experience in global clinical trials and program execution.
Certified Nurse Practitioner, Palliative Care Brigham and Women's HospitalCertified Nurse Practitioner, Palliative CareNewton, MA$49.66–$119.76 / hourThe Nurse Practitioner''s area of practice includes: Assessing the health status of individuals and families by obtaining health and medical histories, performing physical examinations, diagnosing health and developmental problems, and caring for patients suffering from acute and chronic disease by managing therapeutic regimes according to guidelines approved and developed in compliance with 244 CMR 4.22 and, such other additional professional activities as authorized by the guidelines under which a Nurse Practitioner practices. The team reviews medical records, triages consults, collaborates with other healthcare providers, and meets with patients and families to create patient-centered care plans with a focus on symptom management and serious illness conversations or goals of care.
Associate Director, Access Strategy Swedish Orphan Biovitrum ABAssociate Director, Access StrategyWaltham, MARemote$150,000–$195,000 / yearThis role will focus on collaborating with brand marketing team(s) and agency partners to develop tools and resources that support targeted customer segments (e.g., health plans, Medicare, Medicaid, federal, pharmacy, hospital, community practices, Group Purchasing Organizations, etc.). Work closely with internal communications, pricing, policy, legal, health economics outcomes research, and Payer Accounts Teams and Reimbursement teams to ensure the successful implementation of key initiatives.