Biogen Job Trends

About This Role As the Head of Quality for Device and Combination Products, you will lead the development and execution of the global quality strategy, focusing on devices and combination products. This role involves establishing cross-functional roles and serving as the primary quality representative for drug-device combination engagements. You will oversee the Global Quality Device organization, ensuring quality management across all stages from design to lifecycle activities. Your role is critical in ensuring inspection readiness and aligning regulatory regulations within Biogen's quality system, integrating engineering design and risk management. Your leadership will drive compliance with regulatory and quality standards while...

About This Role The Senior Director of HCP Marketing (General Nephrology) will be a critical role and visible leader within the US Nephrology Franchise, leading, planning and executing sophisticated HCP activation and educational strategies for several upcoming launches. Reporting to the Head US Nephrology Marketing, the Senior Director of HCP Marketing will lead the HCP marketing team the development and execution of U.S. branded and unbranded strategies/plans to educate, activate and support nephrologist in identifying post-transplant patients with Antibody-Mediated Rejection (AMR) and Micro-Vasculature Inflammation (MVI) and ensure appropriate referrals to treatment centers; and lead the development of unbranded and branded...

About This Role The Senior Director, Marketing, Rare Disease - Friedreich Ataxia (FA) will be a critical role and visible leader within the organization, leading overall strategy and execution of the FA business within the US. This individual will serve as the US Head and Brand Lead for Friedreich Ataxia. This individual will lead a team of 4-5 professionals and manage US brand strategy and tactics for the continued launch of a first and only medicine for the treatment of Friedreich Ataxia. This professional will lead a cross functional team composed of, but not limited to Business Intelligence and Operations,...

About This Role The Director, Commercial Communications is responsible for leading the narrative for North America’s performance, growth and transformation. This individual will be a strategic leader who develops a deep understanding of our commercial business in North America to drive compelling messaging and education for external and internal stakeholders. Working closely with senior leaders in Communications, Finance, Investor Relations, Operations and the North America leadership team, this role is responsible for the preparation and delivery of informative communications—including talking points, presentations, content and other materials—to prepare the President of North America to help build confidence that the organization is...

Biogen’s Decision & Quality Analytics Innovation (DQAI) team is part of Portfolio Leadership, Analytics & Insights (PLAI), which is under the Development department. The vision of the DQAI team is to deliver trusted insights that drive smarter decisions and measurable impact across the research, development and medical (RDM). We are seeking an experienced and highly motivated Associate Director of Data Management & Stewardship to join our team. This individual will take ownership of managing all aspects of our team’s data - from acquisition and stewardship to governance and cross-functional alignment. The role will ensure that our data foundation is robust,...

About This Role The Senior Clinical Data Manager will serve in a support-level capacity on a Clinical Data Management team to provide efficient and high-quality clinical data management products. Working closely with the Principal Clinical Data Lead, the Senior CDM will ensure that all Data Management activities (from CRF development to Database Lock and eTMF archival) are performed in line with Biogen’s processes. What You’ll Do Support the design, specification, and development of eCRFs, ensuring adherence to Biogen standards throughout. Coordinate the development and testing of clinical data management systems edit checks and listings/reports/tools for data review and discrepancy management...

About This Role The Senior Director of HCP Marketing (Transplant Nephrology) will be a critical role and visible leader within the US Nephrology Franchise, leading, planning and executing sophisticated HCP activation and educational strategies for several upcoming launches. Reporting to the Head US Nephrology Marketing, the Senior Director of HCP Marketing will lead the HCP marketing team the development and execution of U.S. branded and unbranded strategies/plans to educate, activate and support customers treating Antibody-Mediated Rejection (AMR) and Micro-Vasculature Inflammation (MVI). What You’ll Do Serve as U.S. HCP-lead to develop clear HCP strategy, design creative campaigns, develop messaging and coordinate...

About This Role As the Head of Executive Protection and Travel Security, you will lead strategic initiatives that ensure the safety of our senior executives, VPs, and employees during travel. This role is integral to our Global Security team, where you will oversee the design and implementation of advanced security protocols and risk mitigation strategies. Your leadership will be pivotal in developing a comprehensive travel security management program, collaborating with senior leadership to assess and address security threats. Reporting to the Vice President of Global Security, you will play a critical role in aligning security measures with corporate objectives, ensuring...

About This Role The Associate Director, Feasibility (Internal Strategy, Operations, and Process) will play a critical leadership role in driving internal strategy, operational excellence, and process optimization for the Feasibility Center of Excellence (FCoE) function. This role will drive key internal initiatives and help evolve the team’s operating model. The ideal candidate has strong project leadership capabilities, deep strategic feasibility experience, and a passion for continuous improvement and change management. This individual will also serve as a feasibility strategy lead, acting as a key member of study management teams and providing data analysis, enrollment projections, and subject-matter expertise to shape...

About This Role As the Associate Medical Director, Global Drug Safety , you will play a pivotal role in safeguarding patient well-being and shaping the safety strategy for both investigational and marketed products across our portfolio. In this highly visible position, you will serve as a medical and scientific leader within Global Pharmacovigilance, applying your clinical expertise and sound judgment to ensure the highest standards of product safety throughout development and commercialization. What You’ll Do The Associate Medical Director, Global Safety Physician will be responsible for global pharmacovigilance for investigational and/or marketed products, including review and analysis of safety data...

About This Role The Engineer II, Facilities role focuses primarily on temperature-controlled chambers and supports validation activities across the manufacturing facility. You’ll work closely with Facilities, Utilities, Manufacturing, Quality, and Engineering teams to ensure GMP assets are properly commissioned, qualified, and maintained. What You’ll Do Support validation and qualification activities for temperature-controlled chambers and related GMP equipment Assist with the development and execution of IQ/OQ/PQ protocols under guidance from senior engineers Participate in commissioning and qualification of new and existing equipment Support Facilities operations by helping troubleshoot equipment issues and identifying improvement opportunities Assist with change controls, deviations, and CAPAs...

About the Role This application is for a 6-month student role from July - December 2026. Resume review begins in February 2026. Biogen Manufacturing Engineering at the RTP Pharma site supports two sterile filling lines and an Automated Visual Inspection Machine at the Parenteral Facility and a small-scale filling line, Oligonucleotide Synthesis Manufacturing Area, and an Oral Solid Dose Manufacturing Area in Building 35. Manufacturing Engineering helps with design, installation, modification, troubleshooting and qualification of new and existing equipment. Manufacturing Engineering also provides technical support for Manufacturing and other Engineering Departments. What You’ll Do Detailed description of role including but...

About This Role The Associate Medical Director, Scientific & Value Communications role is a part of the US Medical Team, acting as a strategic partner that helps inform medical practice across Multiple Sclerosis and Neuropsychiatry therapeutic areas to improve meaningful patient outcomes. Through development, support and execution of a cross-functionally accepted Scientific Communication Plan, the Associate Medical Director, Scientific & Value Communications will ensure consistent, compliant and impactful communications via publications, congress activities and medical education. This individual contributor role supports Multiple Sclerosis and Neuropsychiatry US marketed products and reports to the Head of Scientific & Value Communications, US Medical....

About the Role This application is for a 12-week internship role from June - August 2026. Resume review begins in February 2026. Biogen’s Health Literacy & Plain Language Center of Excellence (CoE) is seeking a motivated intern in to support various initiatives designed to transform Biogen into a “health literate” organization that disseminates consistent, understandable, and accessible messaging to our patients and the public. The intern selected for this opportunity will learn and apply health literacy and plain language principles to real projects, gaining practical experience in translating complex, scientific jargon into understandable, patient-forward messaging. The intern will also have...

This is a full time, on-site position with a schedule of 12 noon to 12 midnight on a rotating 2-2-3 schedule About This Role The QA Sr Associate I has the working understanding, full knowledge and ability in their primary discipline. They are able to apply technical principles, concepts and understanding of systems and procedures in order to conduct quality and compliance related activities. They are proficient in their understanding of the Biogen Quality Systems. The QA Sr Associate I has working knowledge of GxP regulations and adheres to all regulatory licenses and regulations as well as internal SOPs. The...

About This Role In this role, you’ll provide customer-focused technical support in a fast-paced manufacturing environment, helping keep critical production equipment running safely and efficiently. You’ll perform corrective and preventive maintenance on complex manufacturing systems while collaborating closely with engineering and manufacturing teams. Your work directly supports reliable operations and helps ensure high-quality products that make a real difference for patients. Shift Details 12-hour shifts Nights 6 00 PM – 6 00 AM Rotating 2-2-3 schedule What You’ll Do Perform corrective and preventative maintenance on filling equipment, isolators, vial washers, autoclaves, parts washers, and automatic vial inspection systems Troubleshoot...

About This Role As a Clinical Trial Management PV Lead, you will play a pivotal role in ensuring the operational excellence and strategic oversight of safety processes, contents and data quality within clinical studies. Positioned within our pharmacovigilance team, this role is integral to maintaining compliance with global safety regulations while driving innovation in safety data review and management practices. From utilizing tools and processes for safety database configurations to leading quality reviews of Individual Case Safety Reports (ICSRs), you will be instrumental in shaping our clinical safety initiatives. Your expertise will support cross-functional collaborations, enhance safety data quality, and...

About This Role The Associate Medical Director, Evidence Generation role for rare disease is a part of the US Medical Team, a strategic partner within Biogen, that helps inform medical practice in our rare disease medical team and pipeline to improve meaningful patient outcomes. Through development, support and execution of a cross-functionally accepted Evidence Generation plan, the Associate Medical Director, Evidence Generation will lead the implementation of a cross-portfolio evidence generation plan and successfully deliver the plan using a balance between technical expertise, therapeutic knowledge, project and communication skills, leveraging and prioritizing internal and external resources as required. This individual...

About This Role As a Senior Payroll Specialist within our Global Business Services team, you will play a crucial role in processing payroll for US and Canada, ensuring accuracy and compliance with relevant laws and regulations. Your responsibilities will involve executing payroll processes in a timely manner, troubleshooting systems as needed, and collaborating efficiently with customers and stakeholders. This position is integral to maintaining smooth payroll operations, thereby supporting the company’s overall business objectives. In addition, you will contribute to the enhancement and optimization of payroll systems, continuously improving process documentation. By ensuring all payroll transactions are compliant with internal...

About This Role We are seeking a highly seasoned market access leader to shape U.S. market access strategy for Biogen’s Alzheimer’s portfolio, with a primary focus on Leqembi (IV and sub‑cutaneous). This senior‑level role carries enterprise‑wide visibility, serving as a key advisor to Biogen’s executive leadership, a strategic partner to Investor Relations, and a critical interface with Biogen’s alliance partners. As a strategic integrator across Biogen’s Market Access & Reimbursement (MA&R) organization, Alzheimer’s commercial teams, and alliance counterparts, the Senior Director will influence asset‑level strategy, communicate performance to the highest levels of the company – including the CEO, executive leadership,...

About This Role As the Head of Commercial Field Excellence, you will lead multiple teams dedicated to the strategic alignment, planning, training, and effectiveness of Commercial Excellence across Biogen's North America Portfolio. Your role will be crucial in overseeing enterprise CRM, field systems, and data enablement, supporting Medical field teams. You will drive the enablement and effectiveness of over 800 field employees across diverse therapeutic areas, such as Neurology, Specialty, Rare Disease, and newly emerging areas like Lupus and Kidney. Acting as a key partner to Therapeutic Area Heads and Field Heads, you will enhance field effectiveness and ensure alignment...

About the Role This application is for a 6-month student role from July - December 2026. Resume review begins in February 2026. Our Device Development team is a close-knit group of <8 engineers that design and develop combination products to meet the user needs and pharmaceutical pipeline of Biogen. We are looking for an innovative passionate learner who is ready for both hands-on and documentation engineering work located in Cambridge MA. This co-op position will work on projects that align with Biogen’s culture of pioneering and driving results. What You’ll Do Onsite managing a Device Lab for 3 days a...

This application is for a 12-week internship role from June - August 2026. Resume review begins in February 2026. The Patient Services Analyst intern supports strategic and operational initiatives by delivering rigorous analysis, clear insights, and high-quality executive communications. This role works with complex data to inform decision-making, translates findings into actionable recommendations, and supports high-visibility priorities across the organization. Operating in a fast-paced environment, the role partners closely with cross-functional stakeholders and senior leaders, bringing strong organizational skills, professionalism, and discretion to advance patient services’ performance and experience. What You’ll Do Analyze complex, multi-source data sets related to patient...

About the Role This application is for a 12-week internship role from June - August 2026. Resume review begins in February 2026. As an intern, you are responsible for leading and supporting cross-functional initiatives that enhance patient services operations and experience. The position manages projects from planning through execution, ensuring timely delivery within scope and budget while effectively coordinating stakeholders. This role prepares executive-ready communications, proactively manages risks, and provides clear insights to support decision-making, operating with professionalism and discretion in a fast-paced, high-visibility environment. What You’ll Do Lead the planning, execution, and delivery of patient services initiatives and projects,...

About This Role The Senior Manager, Scientific & Value Communications - Rare Disease role is a part of the US Medical Affairs Team, acting as a strategic partner that helps inform medical practice to improve meaningful patient outcomes. Through development, support and execution of a cross-functionally accepted Scientific Communication Plan, the Senior Manager, Scientific & Value Communications will ensure consistent, compliant and impactful communications via publications, and medical education. What You’ll Do Contribute to the development of successful and compliant execution of the Scientific & Value Communications strategy, including publications (abstracts, posters, manuscripts), digital content, and Field Medical materials. Serve...

About This Role As the Senior Manager of Value Evidence Strategy, you will be integral to designing and executing evidence-generation activities that support both global and regional market access objectives. Positioned within the Global Value & Access Team, you will manage specific research projects focused on real-world evidence, patient-reported outcomes, and health economic modeling. This role requires close collaboration with cross-functional partners, including Market Access, Medical Affairs, Clinical Development, and Epidemiology, to translate evidence into compelling value narratives for stakeholders. Reporting to the Head of Value Evidence Strategy, you'll play a crucial role in coordinating workstreams across sub-functions and leading...

About This Role Our factories run 24/7 operations. Our manufacturing teams work 12-hour shifts (either Days or Nights) on a 2-2-3 calendar rotation. Shift Details 12-hour shifts Nights 600 PM – 600 AM Rotating 2-2-3 schedule The Manufacturing Associate, Lead plays a critical hands-on leadership role within a cGMP manufacturing environment, performing and documenting daily manufacturing operations while ensuring compliance, quality, and efficiency. This role works closely with the Manufacturing Supervisor to coordinate shift activities, allocate resources, and support production, validation, and continuous improvement initiatives. What You’ll Do Execute manufacturing processing steps and manufacturing support activities in accordance with batch...

About the Role This application is for a 6-month student role from July - December 2026. Resume review begins in January 2026. As a co-op, you will be embedded within our dynamic manufacturing team at the Pharma Site, focusing on both Oral Solid Dosage (OSD) and Antisense Oligonucleotide (ASO) facilities. Your role will center around supporting critical projects aimed at continuous improvement and lean six sigma methodologies. As we embark on the journey of introducing new capabilities through the start-up of cutting-edge equipment and facilities, your contributions will be pivotal in driving these efforts forward. You will work closely with...

About This role We are seeking a dynamic and detail-oriented New Product Introduction (NPI) Specialist to join our RTP Bio Manufacturing team. This highly visible role sits within the Manufacturing organization and is responsible for ensuring new products are successfully introduced into the RTP Bio manufacturing facility. The NPI Specialist plays a critical role in driving timelines, coordinating cross-functional stakeholders, and enabling operational readiness to support on-time manufacturing start-up for new products. What you’ll Do Support cross-functional project teams responsible for introducing new products into manufacturing operations. Manage and execute detailed project plans, timelines, and deliverables for NPI initiatives, ensuring...

About This Role We are seeking a highly motivated and creative individual to join our Small Molecule Chemical Development team. This position provides an exciting opportunity to develop robust processes for the synthesis of a wide range of Small Molecules across various modalities. This Scientist II position provides experiences in early phase to late phase drug development and exposure to the design and development of manufacturing processes for clinical and commercial therapeutics. Who We Are We are a team of organic chemists and chemical engineers engaged in the design of innovative processes which supply new medicines to patients. We focus...

About This Role The Sr Manager Case Management, Clinical Trial Safety will be responsible for managing the in-house case processing of clinical trial safety reports (and some post-market reports) in Biogen’s safety database. This role includes hands-on case processing and QC of ICSRs, workflow management, quality management, responsibility for the SMP and team line management. The Sr Manager will ensure consistent, on time and high-quality output of clinical trial ICSRs, working with cross-functional stakeholders. The Sr Manager will report to the Director of Clinical Trial Safety Operations within the Global Case Management function of Safety & Regulatory Operations, Medical Writing...

About This Role As Associate Director, Regulatory CMC Small Molecule Lead, you will play a pivotal role in shaping and executing the global Regulatory Chemistry, Manufacturing and Controls (RegCMC) strategy for Biogen’s small molecule portfolio. You will be responsible for leading cross-functional regulatory CMC activities to ensure timely preparation and delivery of high-quality regulatory submissions that support product development, registration, and lifecycle management. This position requires a strategic thinker and strong communicator with deep regulatory CMC expertise who thrives in a global, matrixed environment. What You’ll Do The Associate Director, RegCMC Small Molecule Lead oversees the management and coordination of...

About This Role The Managed Service Lead is a member of the Head of Access Automation’s leadership team and is accountable for operational excellence for Identity and Access Management (IAM). IAM is a cornerstone of Biogen’s application security, IT GXP/Quality compliance standards and IT user experience. As such, these initiatives underpin Biogen IT’s Drive & Elevate strategy, with a focus on delivering Resilience, Simplification and Scale through continuous improvement of the services that are provided to the entire organization. This Managed Service Lead is required to have subject matter expertise in all aspects of IAM services – especially problem identification...

About the Role This application is for a 6-month student role from July - December 2026. Resume review begins in February 2026. The Immunology Research Unit is focused on the development of therapies for patients suffering from autoimmune diseases. This position offers an opportunity to work with experienced drug discovery scientists as part of a collaborative cross-functional team. The co-op will gain experience in designing and executing hands-on experiments to answer key scientific questions to advance a research program. What You’ll Do As a co-op, you will work side-by-side with experienced scientists to learn and become independent in primary human...

About This Role The Senior Director, Evidence Delivery leads a global organization responsible for transforming clinical data into high-quality, actionable evidence across the clinical development portfolio. This role drives the strategy, innovation, and operational excellence behind submission-ready datasets, analyses, and visualizations that support regulatory, market access, and publication needs. The Senior Director champions modernization through open-source programming, advanced analytics, automation, and AI/ML. Reporting within SPDDS and QSDO, this leader ensures regulatory compliance, inspection readiness, and continuous improvement while building a future-ready evidence delivery organization. What You’ll Do Define and execute the global Evidence Delivery strategy aligned with clinical development and...

About This Role As an Associate II in Inventory Control, you will be a vital part of the Maintenance Reliability team, providing expert planning and parts support to the site. Your role will involve procuring essential parts, managing inventory, and linking assets to optimize operations. You will be responsible for CMMS (Computerized Maintenance Management System) planning and inventory management, ensuring seamless preventive maintenance procedures. This position is integral to maintaining the efficiency of mechanical equipment, supporting Maintenance, Manufacturing, Metrology, and Engineering teams. By managing small projects and programs related to inventory operations, you will ensure that all inventory-related issues for...

About the Role This application is for a 12-week internship role from June - August 2026. Resume review begins in January 2026. The Biogen Epidemiology group contributes to the mission and goals of Biogen by providing a deep understanding of patient populations and the burden of disease throughout the drug development life cycle. This is accomplished by synthesizing existing knowledge as well as designing and conducting studies related to disease prevalence and drug safety and effectiveness. The group of approximately 14 Ph.D.-level epidemiologists is organized by disease units and deployed to drug development and other internal teams. The Epidemiology team...

About the Role This application is for a 6-month student role from Jun-Dec. Resume review begins in January 2026 As a Co-op in the Supply Chain team, you will assist with initiatives to synchronize material management across multiple platforms. You will play a key role in the “BOM Harmony” project, which aims to harmonize bills of materials across systems such as EBS, PLM, BPRs, and ASCP. This position offers hands-on experience in cross-platform supply chain management, data harmonization, and process improvement within a leading pharmaceutical organization. What You’ll Do As a co-op, you will Support the “BOM Harmony” project to...

About the Role This application is for a 6-month student role from July - December 2026. Resume review begins in February 2026. Neurodevelopmental Biology Research Group is seeking a highly motivated co-op student to support exploratory research focused on therapeutic strategies to treat Friedreich's ataxia. This role is situated within early-stage research efforts dedicated to target identification and validation. The successful candidate will work closely with scientists to design, execute, and analyze experiments that investigate targeting key DNA, RNA, and protein sequences that may alter the disease course or relevant pathways. Key responsibilities include performing molecular assays such as quantitative...

About the Role This application is for a 6-month student role from July - December 2026. Resume review begins in February 2026. The Neurology Research Unit, ALS Research Group, is seeking a highly motivated co-op student to support exploratory discovery research focused on the molecular and cellular mechanisms underlying ALS. This role is situated within early-stage research efforts dedicated to target identification and target validation and provides the opportunity to contribute to hypothesis-driven studies addressing fundamental questions in ALS biology. The successful candidate will work closely with scientists to design, execute, and analyze experiments that investigate genomic and proteomic alterations...

About the Role This application is for a 12-week internship role from June - August 2026. Resume review begins in February 2026. Statistical Programming (SP) is part of the R&D organization at Biogen. As a Statistical Programming intern, you will gain hands-on experience in programming and analysis processes used in clinical trials. In this role, you will learn data manipulation, analysis, and reporting of clinical trial data. This internship is designed to provide you with foundation knowledge in regulatory requirements, as well as exposure to the broader clinical trial process, all while supporting our mission of advancing medications that improve...

About This Role The Executive Assistant to the Head of the West Coast Hub (WCH) will be a highly proactive, collaborative, and self‑motivated professional responsible for direct administrative support and coordination to the Head of WCH. This role serves as a central connector for the Hub’s leadership team and plays a key role in enabling smooth operations and execution across the site and across Biogen. The Executive Assistant will partner closely with the Head of Strategy, Operations, and Excellence and work as part of a tightly integrated team with the other WCH Executive Assistants, Office Manager, IT, and site facilities...

About the Role This application is for a 12-week internship role from June - August 2026. Resume review begins in February 2026. As an intern, you will join the Global Network Strategy and Planning department. The Network Strategy team provides strategic decision support and risk management to Biogen’s Pharmaceutical Operations and Technology (PO&T) division, which is responsible for advancing our therapeutic pipeline and ensuring reliable supply of our commercial therapies to patients. What You’ll Do The intern will lead the effort to strengthen business analytical tools and frameworks for strategy development by partnering with leaders in the network strategy team,...

About the Role This application is for a 12-week internship role from June - August 2026. Resume review begins in February 2026. The Global Environmental, Health & Safety (EHS) team is seeking a motivated and detail-oriented intern to support strategic initiatives that advance Biogen’s global EHS programs and sustainability goals. This role offers a unique opportunity to gain exposure to enterprise-level EHS systems, global compliance frameworks, and programs that shape Biogen’s proactive safety culture across all regions and functions. You will work directly with global EHS leaders on projects that strengthen governance, enable data-driven decision-making, and support continuous improvement across...

About the Role This application is for a 12-week internship role from June - August 2026. Resume review begins in February 2026. As an intern in the Manufacturing Supply Chain team, you will assist with initiatives focused on optimizing safety stock levels and ordering practices for non-BOM (Bill of Materials) materials. Your work will help ensure successful procurement, streamline ordering schemes related to raw material testing, and prevent overstocking. You will also support master data review and confirm the accuracy of materials needed for production runs. This role offers hands-on experience in supply chain management, data analysis, and process optimization...