Senior Manager, IT Business Applications - Japan Insmed, Inc.Senior Manager, IT Business Applications - JapanJapan, MOAs a global biopharmaceutical company dedicated to transforming the lives of patients with serious and rare diseases, you'll be part of a community that prioritizes the human experience, celebrates curiosity, and values every person's contributions to meaningful progress. We are looking for a driven, results-oriented leader to lead the effort in building Insmed's next generation of systems used to automate and optimize our critical Japan business applications and processes.
Medical Strategy Lead (Ntm) Insmed, Inc.Medical Strategy Lead (Ntm)Japan, MOGovernance: Lead the review and decision processes locally (e.g., Japan Medical Review Committee (J-MRC), Japan Commercial Review Committee (J-CRC), Japan Grant Review Committee (J-GRC), JMA review of Medical Information Letter) and globally (e.g., Arikayce Medical Affairs Team (AMAT), Insmed Medical Affairs Research Review Committee (IMARRC), Integrated Evidence Team (IET) meeting). What You'll Do: Excellence in strategy: Partner with Medical Affairs Leadership Team (MALT), Medical Affairs Team (AMAT), global / local internal business partners, including commercial partners, and external stakeholders to plan and execute GK Brand Plan, strategies / tactics defined in JMAP for product.
Manager/Sr. Manager, Drug Safety & PV Insmed, Inc.Manager/Sr. Manager, Drug Safety & PVJapan, MOAbout the Role: This role is mainly responsible for participating in the Drug Safety and Pharmacovigilance activities including operational works on Pharmacovigilance (PV) and Post-Marketing Study (PMS); training related to PV and PMS activities; quality control and assessment on PV and PMS activities; record management on PV and PMS activities; vendors/temporary staff management, and supporting for communication with regulatory authorities. What You'll Do: Participate in ICSR case management, as well as the maintenance of safety database and establishment of the processes of handling case reports with safety database, lead the process for local aggregate safety reports including J-DSUR and ensure all regulatory safety documents are processed and submitted according to regulatory requirements and timelines.
Associate Director, Pharmacovigilance/ Product Safety Insmed IncAssociate Director, Pharmacovigilance/ Product SafetyNJRemote$179,000–$232,500 / yearFor New York City Residents: To assist in identifying candidates with qualifications matching those required and/or preferred for this role, Insmed uses an Automated Employment Decision Tool ("AEDT") that employs artificial intelligence to analyze and score information provided in resumes and application materials including, but not limited to, skills, work experience, education, and job-related qualifications. Author, review and provide input and approval for drug-safety related regulatory reports and clinical study documents including clinical study protocols, Informed Consent Forms, Investigator Brochures, Integrated Summary of Safety (ISS), Integrated Summary of Efficacy (ISE), MedDRA coding of AEs, product package and labeling.
Senior Specialist, Supplier Quality Insmed IncSenior Specialist, Supplier QualityNJRemote$100,000–$126,500 / yearAbout the Role: Reporting to Director, Supplier Quality, the Senior Supplier Quality Specialist will be responsible for the lifecycle management of Quality Technical Agreements (QTAs) with suppliers, contract manufacturers, and service providers, and for leading and executing GMP audits of external suppliers as primary responsibility with additional support of core supplier quality activities such as supplier qualification, GMP certificate management, and supplier scorecards as assigned. The ideal candidate has a strong working knowledge across the supplier quality programs such as supplier qualification, supplier risk management, external supplier audits, and supplier notifications, and brings sound judgment, negotiation skill, and cross-functional collaboration to ensure suppliers consistently meet company and regulatory quality expectations.
Director, Diagnosis Innovation & Collaboration Insmed IncDirector, Diagnosis Innovation & CollaborationNJRemote$177,000–$242,000 / yearAs a global biopharmaceutical company dedicated to transforming the lives of patients with serious and rare diseases, you'll be part of a community that prioritizes the human experience, celebrates curiosity, and values every person's contributions to meaningful progress. Excellent communication skills and strong analytical skills required to understand scientific data, recognize key business issues and prepare high-level presentations for senior executives.
Senior Manager, GCP, GLP Supplier Quality Insmed IncSenior Manager, GCP, GLP Supplier QualityNJRemote$124,000–$161,000 / yearAnalyze supplier quality data and performance trends, including deviations, CAPAs, audit findings, inspection outcomes, data integrity issues, and timeliness metrics, and facilitate, in collaboration with functional representative supplier governance forums and business reviews to drive remediation actions, corrective measures, and continuous improvement while maintaining accurate supplier records and approved supplier listings. Partner with DevQA to develop, manage, and continuously improve supplier performance monitoring frameworks for GCP and GLP suppliers in collaboration with the functional representatives, including KPIs, scorecards, and quality metrics, ensuring accurate risk-based scoring, timely completion, and appropriate control alignment.
Director, Field Strategy Insmed IncDirector, Field StrategyBridgewater, NJRemote$177,000–$242,000 / yearWho You Are: You have a Bachelor's Degree along with 10+ years of progressive pharmaceutical commercial experience (sales, commercial strategy, commercial operations, leadership, marketing, market access, or commercial excellence), or a combination of education, training, and experience. You''ll act as the liaison between field-based teams and Global Program Teams, ensuring commercial strategies are informed by field insights while providing thought leadership in field force sizing, targeting, call planning, organizational design, and strategic enablement.
Associate Director Medical Science Liaison -Southeast FL Insmed IncAssociate Director Medical Science Liaison -Southeast FLFort Lauderdale, FLRemote$187,000–$244,000 / yearKey responsibilities include conducting scientific exchanges, presenting product data, supporting advisory boards, gathering HCP insights, assisting with clinical trial activities, and delivering internal training to colleagues - all in alignment with Insmed''s Medical Affairs plans and a patient-first mission. Work closely with Insmed personnel to ensure adequate training, access to educational resources and alignment between Insmed's medical affairs plans and the unmet needs of the patients and healthcare professionals and be responsible for maintaining annual expenses within assigned budget parameters.
Associate Director, Medical Science Liaison - Los Angeles/Southern California Insmed IncAssociate Director, Medical Science Liaison - Los Angeles/Southern CaliforniaRiverside, CARemote$187,000–$244,000 / yearWork closely with Insmed personnel to ensure adequate training, access to educational resources and alignment between Insmed's medical affairs plans and the unmet needs of the patients and healthcare professionals and be responsible for maintaining annual expenses within assigned budget parameters. Key responsibilities include conducting scientific exchanges, presenting product data, supporting advisory boards, gathering HCP insights, assisting with clinical trial activities, and delivering internal training to colleagues - all in alignment with Insmed''s Medical Affairs plans and a patient-first mission.
Director, Access Programs Insmed IncDirector, Access ProgramsBridgewater, NJRemote$177,000–$242,000 / yearReporting to the Executive Director, Head of Channel, Distribution and Access Programs, you'll be responsible for the strategy and management of Insmed's Patient Assistance and Copay programs, focusing on optimization of program business rules, strategic vendor management and data insights to manage appropriate patient affordability solutions. This role serves as the primary business owner of the affordability programs and vendors as well as cross-functional work with Market Access, Finance, Legal, Compliance and Product Teams to deliver patient solutions aligned with business objectives.
Director, Product Communications Insmed IncDirector, Product CommunicationsNJ$177,000–$242,000 / yearThe Director will sit on the ARIKAYCE Extended Global Program Team and partner closely with Global Program Head, commercial, clinical development, patient advocacy, and medical teams to design and execute communications strategies and plans, including disease state awareness, market prep, data communications, and regulatory milestones. New Indication Launch Communications: Lead the development and execution of a comprehensive communications strategy to prepare for and launch ARIKAYCE's potential new indication, including pre-launch market preparation, launch day activation, and post-launch momentum building.
Senior Manager, Learning & Development Insmed IncSenior Manager, Learning & DevelopmentNJ$124,000–$161,000 / yearThis role collaborates closely with stakeholders, HR Business Partners, and the broader L&D team, leveraging data, insights, and feedback to address leadership and power skill development needs to ensure learning solutions are aligned with organizational goals, grounded in adult learning principles, and delivered with excellence across multiple modalities and global audiences. Lead the design, development, and management/administration of cohort-based learning programs, including program architecture, participant journey mapping, and ongoing cohort facilitationManage the full lifecycle of cohort programs, including participant enrollment, communications, scheduling, facilitator coordination, and post-program evaluation.
Early Development Program Lead - Cambridge Insmed IncEarly Development Program Lead - CambridgeCambridge, MARemote$255,000–$347,500 / yearWhat You'll Do: In this role, you'll have the opportunity to serve as the primary bridge between the Cambridge Research organization and Insmed's Development functions; lead and coordinate cross-functional early development project teams spanning medicinal chemistry, CMC, formulation, biology, toxicology, DMPK/ADME, translational science, regulatory, clinical, and patient advocacy. Author and review key program documents including early TPPs, project charters, integrated development plans, and support of any regulatory briefing documents; present program status and support presentations of scientific findings to internal leadership.
Director, Marketing - Expert Engagement & Regional Marketing Insmed IncDirector, Marketing - Expert Engagement & Regional MarketingNJRemote$177,000–$242,000 / yearReporting to the Global Commercial Lead, you''ll coordinate the commercial U.S. expert leader strategy, drive awareness among the HCP community, and lead regional marketing across Pulmonary Arterial Hypertension (PAH), Pulmonary Hypertension associated with Interstitial Lung Disease (PH-ILD), Idiopathic Pulmonary Fibrosis (IPF), and Progressive Pulmonary Fibrosis (PPF). Who You Are: You have a minimum Bachelor's degree (MBA or advanced degree preferred) along with 8-10+ years of experience in pharmaceutical/biotech commercial roles, including 5+ years in U.S. regional marketing, sales, and HCP/expert engagement, or a combination of education, training, and experience.
Associate Director, Medical Science Liaison - Los Angeles/Southern California Insmed IncAssociate Director, Medical Science Liaison - Los Angeles/Southern CaliforniaLas Vegas, NVRemote$187,000–$244,000 / yearWork closely with Insmed personnel to ensure adequate training, access to educational resources and alignment between Insmed's medical affairs plans and the unmet needs of the patients and healthcare professionals and be responsible for maintaining annual expenses within assigned budget parameters. Key responsibilities include conducting scientific exchanges, presenting product data, supporting advisory boards, gathering HCP insights, assisting with clinical trial activities, and delivering internal training to colleagues - all in alignment with Insmed''s Medical Affairs plans and a patient-first mission.
Senior Analyst, Quality Assurance (Analytical) Insmed IncSenior Analyst, Quality Assurance (Analytical)San Diego, CA$100,000–$126,500 / yearYou will serve as the primary QA point of contact for assigned products or laboratory functions, independently managing routine quality oversight and laboratory record approvals while escalating complex, high-risk, or strategic matters to QA leadership as appropriate. Who You Are: You have a minimum of a Bachelor's degree in in Chemistry, Engineering, Life Sciences, or a related discipline along with 5+ years of experience in Quality Assurance experience within the pharmaceutical or biotechnology industry, preferably supporting Quality Control operations.
Director, Compensation Insmed IncDirector, CompensationNJ$177,000–$242,000 / yearAs a global biopharmaceutical company dedicated to transforming the lives of patients with serious and rare diseases, you'll be part of a community that prioritizes the human experience, celebrates curiosity, and values every person's contributions to meaningful progress. What You'll Do: In this role, you will serve as a trusted advisor to HR Business Partners and functional leaders, providing strategic guidance on compensation philosophy, market competitiveness, pay decisions, promotions, and organizational changes.
Senior Director, Medical Affairs - Respiratory Insmed IncSenior Director, Medical Affairs - RespiratoryNJRemote$273,000–$372,000 / yearThe Senior Director will also develop and lead medical affairs activities ensuring partnership within the team (medical strategy, scientific communications and publications) all key Medical Affairs functions (Medical Excellence, HEOR, Field Medical, Medical Information) as well as maintaining a high-level cross-functional collaboration across the organization to ensure alignment and One Insmed approach. Company Learning Institute providing access to LinkedIn Learning, skill building workshops, leadership programs, mentorship connections, and networking opportunities.
Associate Director, Regulatory Affairs, Post Approval Insmed, Inc.Associate Director, Regulatory Affairs, Post ApprovalJapan, MOAbout the Role: The Associate Director, Regulatory Affairs - Post-Approval is responsible for leading regulatory activities related to approved products in Japan and for leading Japanese specific regulatory operational activities. This position serves as the regulatory lead for post-approval compliance, ensuring products remain compliant with the Pharmaceuticals and Medical Devices Act (PMD Act) and other applicable Japanese regulations while supporting commercial and medical initiatives.