Associate Medical Director Hematology, US OBU Medical Affairs 3310 Takeda Pharmaceuticals U.Associate Medical Director Hematology, US OBU Medical AffairsBoston, Massachusetts$169,400–$266,200 / yearThe 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. This role involves monitoring regulatory developments, ensuring compliance, and preparing regulatory documents to support Takeda's mission of delivering transformative therapies to patients.
Director, Government Legislative Affairs BlueCross and BlueShield of MassachusettsDirector, Government Legislative AffairsBoston, MA$198,360–$242,440 / yearDirectly advocate for the Company's interests in legislative hearings, regulatory sessions, and one-on-one meetings with legislators, regulators, and staff on issues impacting health care and the insurance industry, including behavioral health and substance use disorder treatment, prescription drug pricing and transparency policy, provider payment policy, municipal health reform, and utilization management tools. In-depth demonstrated knowledge and understanding of the health care and health insurance industry, including specific issue-area expertise in public policy related to behavioral health, substance use disorder, prescription drug pricing and transparency policy, provider payment policy, municipal health reform, and utilization management tools.
Director of Clinical Affairs Eight SleepDirector of Clinical AffairsBoston, MassachusettsThis is a hands-on, operationally intense position for someone who knows how to stand up a study from scratch, manage third-party clinical sites, write IRB and informed consent documents, oversee data management, establish and oversee any study committees (EC, DSMB, etc.), prepare for FDA submissions and audits, and drive studies to completion on time and on budget. 10+ years of hands-on clinical operations experience, with at least 5 years of experience in leadership roles, executing clinical studies for FDA-regulated medical devices, SaMD/digital health products, or combination products.
Director Of Clinical Affairs Eight SleepDirector Of Clinical AffairsBoston, MA$200,000–$250,000 / yearThis is a hands-on, operationally intense position for someone who knows how to stand up a study from scratch, manage third-party clinical sites, write IRB and informed consent documents, oversee data management, establish and oversee any study committees (EC, DSMB, etc.), prepare for FDA submissions and audits, and drive studies to completion on time and on budget. 10+ years of hands-on clinical operations experience, with at least 5 years of experience in leadership roles, executing clinical studies for FDA-regulated medical devices, SaMD/digital health products, or combination products.
Medical Director, Medical Affairs Beeline MedicinesMedical Director, Medical AffairsBoston, Massachusetts$266,000–$344,000 / yearLead and conduct peer-to-peer scientific exchange with KMEs, investigators, and HCPs together with the development team— sharing clinical and emerging data, discussing unmet medical needs, and gathering external insights (such as in depth knowledge of the patient journey from diagnosis to treatment along with barriers that are encountered along the way) that inform medical strategy, pipeline positioning, and commercial readiness. Partner with Field Medical Affairs and MSL teams to ensure accurate, balanced, and up-to-date scientific tools and resources are available and consistently applied in field engagements — participating directly in key field interactions when the scientific complexity or stakeholder importance warrants senior medical presence.
Consulting Associate/Strategy & Medical Affairs (Life Sciences) CRA International, Inc.Consulting Associate/Strategy & Medical Affairs (Life Sciences)Boston, MA$110,000–$126,500 / yearWe work with life sciences organizations directly, as well as with their legal counsel, industry associations, government organizations, and advocacy groups from the earliest stages of research into new therapy areas, through clinical development, to the launch of therapies that will achieve commercial success and fulfill the expectations of our clients and their key stakeholders. CRA's Life Sciences practice helps pharmaceutical, biotechnology, diagnostics, and medical device companies achieve optimum performance across key aspects of their business, including innovation, commercial success, organization, and reputation, all for the long-term benefit of patients, clinicians, employees, and shareholders.
Senior Director - US Medical Affairs - Nephrology Vertex PharmaceuticalsSenior Director - US Medical Affairs - NephrologyBoston, MassachusettsServe as the primary internal medical-scientific authority for the assigned asset, providing scientific interpretation of data (clinical trials, real-world evidence, published literature) and translating insights into actionable medical strategy. This role provides scientific leadership and strategic direction across cross-functional teams, ensuring medical strategies are aligned with corporate objectives, patient needs, and the evolving US treatment landscape.
Lead, US Public Affairs & Patient Advocacy Rare Diseases SanofiLead, US Public Affairs & Patient Advocacy Rare DiseasesCambridge, MA$122,250–$176,583.33 / yearCross-Functional Collaboration: Act as the patient advocacy liaison to internal cross-functional teams including Medical Affairs, Regulatory Affairs, Market Access, Health Economics & Outcomes Research (HEOR), Clinical Development, Commercial, and other functions of Corporate Affairs. Job Category Description: Dedicated to US rare disease and rare blood disorders portfolio engaging with patient organizations, scientific societies, and associated institutions to build meaningful partnerships, support disease awareness, and ensure the patient voice is integrated into Sanofi's rare disease strategy.
Director, Scientific Communication and Operations, Medical Affairs Kymera TherapeuticsDirector, Scientific Communication and Operations, Medical AffairsWatertown, MA$195,000–$275,000 / yearThe Director Scientific Communication and Operations, Medical Affairs, reporting into the Vice President, Medical Affairs, is a strategic leader responsible for developing and executing Medical Affairs strategy across Medical Affairs Scientific Communications and Operations, spanning data generation and dissemination, scientific publications, medical-to-medical content development, and field medical training materials, as well as operational planning, congress planning, grants and sponsorships, cross-functional coordination, and advisory boards. This role will work cross-functionally with internal stakeholders (R&D, Commercial, Regulatory, etc.) and externally with healthcare professionals, key opinion leaders (KOLs), and scientific organizations to ensure impactful and compliant medical engagement and education aligned with corporate objectives.
Global Medical Director, Medical Affairs Dyne TherapeuticsGlobal Medical Director, Medical AffairsWaltham, MA$215,000–$260,000 / yearThis individual translates clinical and scientific insights into actionable medical strategies, supports congress, symposia, advisory board, publication, medical education, and evidence generation activities, and helps strengthen Dyne’s external scientific presence with healthcare professionals, key opinion leaders, payers, patient communities, and other stakeholders. The Global Medical Director partners closely with Clinical Development, Clinical Operations, Regulatory Affairs, Scientific and Medical Communications, Value and Access, Commercial, Patient Advocacy, regional medical teams, and external experts to ensure medical plans are aligned with corporate, program, product, and regional priorities.
Head, US Public Affairs & Patient Advocacy, Immunology SanofiHead, US Public Affairs & Patient Advocacy, ImmunologyCambridge, MA$232,500–$335,833.33 / yearThe Head, US PA&PA Immunology carries deep therapeutic area leadership combined with enterprise-level contribution: Therapeutic area leadership: owns the US advocacy strategy and outcomes for the full Immunology portfolio, Dupixent across dermatology, respiratory, rhinology, gastrointestinal and Type 2 inflammation indications, plus Sanofi's non-alliance immunology assets and pipeline. Accountable for Sanofi's trusted partnerships with the US advocacy community across the immunology therapeutic area, owning the health, depth, and outcomes of relationships with patient advocacy organizations and professional societies, and earning continued partnership through transparency, consistency, and the quality of collaboration in service of shared patient priorities.
Vice President, Medical Affairs Oncology Parabilis MedicinesVice President, Medical Affairs OncologyCambridge, MA$360,000–$410,000 / yearThis senior executive leader is accountable for the end-to-end design and execution of the Medical Affairs strategy across Parabilis portfolio, including Scientific Communications, Medical Education, Evidence Generation, Key Opinion Leader (KOL) Engagement, Publication Planning, and Medical Information. We are fiercely independent as a leader in defying the limitations of current therapeutic modalities, and interdependent as a team as we work collaboratively to shift drug discovery paradigms and provide patients with better treatment options.
Head of Medical Information (Director/Senior Director) – Medical Affairs Vor BioHead of Medical Information (Director/Senior Director) – Medical AffairsBoston, MA$220,000–$240,000 / yearAs the most senior person in the function the MI lead will be accountable for leading the strategy and operations of the MI function, ensuring accurate, timely, and compliant responses to inquiries from healthcare professionals (HCPs), patients, and internal stakeholders, and be the primary point of accountability with other functions across the company (including, among others, compliance, quality, and safety & pharmacovigilance). Senior Director level: 12+ years of relevant experience in MI or related MA roles within the pharmaceutical or biotechnology industry, with at least 3 years of management or team leadership experience managing direct reports and/or matrixed teams.
Head Of Medical Information (Director/Senior Director) - Medical Affairs Vor Biopharma Inc.Head Of Medical Information (Director/Senior Director) - Medical AffairsBoston, MA$220,000–$240,000 / yearAs the most senior person in the function the MI lead will be accountable for leading the strategy and operations of the MI function, ensuring accurate, timely, and compliant responses to inquiries from healthcare professionals (HCPs), patients, and internal stakeholders, and be the primary point of accountability with other functions across the company (including, among others, compliance, quality, and safety & pharmacovigilance). Senior Director level: 12+ years of relevant experience in MI or related MA roles within the pharmaceutical or biotechnology industry, with at least 3 years of management or team leadership experience managing direct reports and/or matrixed teams.
Senior Manager, Strategy - Medical Affairs Azurity Pharmaceuticals - USSenior Manager, Strategy - Medical AffairsWoburn, MAMedical 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 30+ 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.
Regional Government Affairs Director - Northeast ModivCareRegional Government Affairs Director - NortheastLynn, MA$159,900–$215,900 / yearThe position will design and implement state-level advocacy strategies aligned with enterprise priorities and will manage engagement with key stakeholders and execution of public affairs initiatives as directed and designed in collaboration with Corporate Affairs leadership. Serves as the company's primary representative at the assigned state capitols before executive leadership, including Medicaid directors, transportation program leaders, and personal care services (PCS) administrators.
Director - Medical Affairs Integrated Resources, IncDirector - Medical AffairsMarlborough, MassachusettsFull timeQualifications: MD with postgraduate specialization in Infectious Diseases or Immunology Industry experience of 5 or more years strongly preferred Experience in the conduct of clinical trials preferred Proficiency in critical data review and interpretation Excellent analytical and interpretative skills and ability to develop and translate medical affairs strategies into actions Matrix leadership of cross-functional teams Excellent oral and written communication skills, including facilitation of interactive discussions and presentations to large and diverse audiences, including thought leaders Customer focus and credibility with customers Cultural sensitivity, international experience and more than one spoken language are advantages Availability to travel (approx. Provide high quality clinical input in disease-specific strategy plans, as well as publications, educational materials, study protocols, steering committee and advisory board meeting objectives, medical information letters, commercial planning, and on scientific educational grant requests and patient advocacy grant requests.
Senior Medical Science Liaison - Gene Therapy US Medical Affairs, Northeast Orchard Therapeutics plcSenior Medical Science Liaison - Gene Therapy US Medical Affairs, NortheastBoston, MARemoteDevelop a territory profile including Centers of Excellence, key expertise, newborn screening approaches and leaders, and market access pathways to inform medical strategy and tactical planning in collaboration with our Commercial, Diagnostic, and Patient Advocacy partners. As a field-based member of the medical affairs team, the Sr MSL will be responsible for developing and enhancing professional relationships with external thought leaders involved in all phases of the clinical development process through a fair-balanced and high-value exchange of clinical and scientific information.
NewSr. Director, Medical Affairs Pivotal SolutionsSr. Director, Medical AffairsBoston, MassachusettsThis role oversees the development and implementation of medical affairs plans, provides scientific and clinical expertise, and ensures the communication of accurate and balanced scientific information to healthcare professionals and stakeholders. Director of Medical Affairs plays a pivotal role in bridging the gap between clinical development and commercial operations, ensuring that medical strategies align with broader organizational goals.
Leader Medical Affairs Canon USA & AffiliatesLeader Medical AffairsBoston, MARemote10 years’ experience as a Medical Physicist, Scientist, or MD in a clinical hospital or clinical research setting or 3 years of experience as a Medical Physicist, Scientist, or MD in a clinical hospital or clinical research setting plus 7 years of experience in healthcare industry as imaging scientist or research manager. Analyze and communicate technical and clinical product specification requirements from luminaries, market research teams, and via Medical Advisory Boards (MABs) to global business team.