Biogen Job Trends

About This Role As a Senior Manager, Regulatory CMC Lead, you will provide regulatory CMC expertise to support assigned projects and products, contribute to global CMC regulatory strategy, and where appropriate, lead regulatory submissions and related strategic activities. You will be part of a dynamic team, collaborating closely with the CMC Global Regulatory Lead and key stakeholders to compile and prepare submissions/documentation for biologics projects. Your role will involve managing routine and non-routine regional Health Authority interactions, serving as the primary global contact for regulatory CMC activities. In late-stage development programs, you will be the contact for assigned regions, ensuring...

About This Role As the PO&T Risk Management Lead, you will establish and lead integrated risk management processes crucial to identifying top-level risks across PO&T accountabilities. This role is pivotal in synthesizing, escalating, and communicating technology, quality, supplier, safety, environmental, product supply, compliance, and emerging risks to the PO&T leadership team. You will engage with both internal and external sites within Biogen’s manufacturing and supply network to apply standardized frameworks for risk impact assessments. The position involves collaborating with the PO&T leadership to approve mitigation plans for critical risks and regularly reporting on organizational preparedness. Your efforts will help advance...

About This Role The Senior Report Developer is responsible for the development and maintenance reports for use in clinical trials, load data from various sources into data warehouse, program custom mappings and develop custom visualizations for ongoing data review. This Role will be responsible for the development of Standard Reports catalogue (e.g. exception listings, clean patient tracker etc.) used for data review and reconciliations by the DM Operations staff and is responsible for some Automation Projects such as workflow for common data management programming and validation purposes. Serves as a point of contact for the assigned project. Attends meetings, participates...

About This Role Biogen’s Marketing teams are on the front lines every day, ensuring that our products have the right visibility for the patients who need them most. We work from a deep understanding of the science behind our therapies and the disease areas that they treat. The Associate Director of Marketing will play a pivotal role in shaping and executing strategic initiatives to prepare for the US launch of Lupus product in both cutaneous and systemic lupus erythematosus (CLE and SLE). This highly visible role requires a blend of strategic insight, marketing acumen, and operational excellence to deliver impactful...

About the Role This application is for a 6-month student role from July - December 2026. Resume review begins in January 2026. Clinical Pharmacology and Pharmacometrics (CPP) plays a central role in determining the right dose of the right molecule for the right patient by applying pharmacology principles, quantitative modeling, and simulations. CPP contributes across the entire drug‑development continuum—from pre‑R2D through regulatory submission, approval, and life‑cycle management. The function generates quantitative insight into what the body does to the drug (pharmacokinetics) and what the drug does to the body (pharmacodynamics), enabling prediction of benefit–risk, accelerating development, and informing regulatory strategy....

About This Role The Category Manager is responsible for procurement support for the Patient S ervices organization and the Commercial Print and Fulfillment Services Category . The c ategory cover s a variety of patient support programs critical to treatment , education and securing access to Biogen medications. In addition to Patient Services, the role covers Print and fulfillment services for the Commercial organization that include Print, fulfillment, sample program and patient letters. T he individual will be responsible for stakeholder management, procurement category management, sourcing, contract negotiation and supplier relationship management . This is an individual contributor role that...

About This Role The Principal Clinical RBQM Programmer is responsible for implementing and maintaining RBQM statistical monitoring solutions to support Risk-Based Quality Management (RBQM) strategies in clinical trials. This role involves configuring RBQM platforms, interpreting outputs, and collaborating with Data Management and Clinical Operations teams to ensure data integrity and compliance with regulatory standards. The position also supports integration of RBQM system with other clinical systems and contributes to continuous improvement initiatives for data quality oversight. What You’ll Do Configure and maintain RBQM platform for assigned clinical studies (including Key Risk Indicators, Quality Tolerance Limits & Data Quality Analysis) Execute...

About the Role This position is for a 12-week internship role from June - August 202 6 . Resume review begins in January 202 6 . Biogen develops medicines for debilitating medical conditions with the goal of making a meaningful difference in patients’ lives . The Global Clinical Supply Chain Team plays an integral role in helping patients gain access to best-in-class medicines . What You’ll Do As an intern in the Global Clinical Supply Chain Team, you will be exposed to a variety of operations and get a firsthand view of what it takes to manufacture and deliver the...

About the Role This application is for a 6-month student role from July - December 2026. Resume review begins in January 2026. The Genomics and Computational Biology team performs high-quality computational analyses on genomics/transcriptomics datasets, develops robust NGS data analysis pipelines, and evaluates cutting edge computational tools and technologies. Using such approaches, we collaborate closely with all discovery teams across Research to address critical drug development questions related to target identification and validation, drug mechanism of action, and the underlying disease biology. Data types frequently analyzed within our group include RNAseq, miRNAseq, sc/snRNAseq, spatial transcriptomics and proteomics derived from patient...

In this field based, specialty sales representative position you will be called upon to sell our Neurology products with key stakeholders in the Multiple Sclerosis community including Neurologists, allied health professionals, and local MS chapters. The Sr. Territory Business Manager is responsible for developing and executing on sales plans for their assigned territory. Candidates can be considered for Sr. Territory Business Manager or Territory Business Manager base on qualification outlined below. What You'll Do You will convey complex clinical and reimbursement information to customers and key stakeholders regarding Biogen products. You must be able to utilize exemplary interpersonal skills and...

About the Role This application is for a 6-month student role from July - December 2026. Resume review begins in January 2026. The Global Trade Compliance team’s mission is to enable Biogen’s purpose and commitment to patients, shareholders and communities by managing risks, creating values, driving excellence in execution and critical capabilities. We do this by ensuring that all our products (finished drugs, drug substances, clinical samples, etc.) move across multiple countries in compliance with international trade regulations and without delays. Global Trade Compliance also pays a key role across Biogen’s end to end business planning by completing due diligence...

About the Role This application is for a 12-week internship role from June - August 2026. Resume review begins in January 2026. The Business Operations Team serves as the strategic and operational backbone of the West Coast Hub, ensuring the seamless execution of clinical development and translational science. Our mission is to bridge the gap between high level strategy and daily execution across four core pillars Technology & Analytics, Contractual Infrastructure, External Alliances, and Organizational Advocacy. Through targeted software solutions, robust site and investigator agreement management, and the cultivation of high‑impact academic and biotech partnerships, we provide the infrastructure and...

About the Role This application is for a 12-week internship role from June - August 2026. Resume review begins in January 2026. We are seeking a motivated and detail-oriented intern to support two key initiatives within our planning and operations function Process Automation & Efficiency (PEI Project) Contribute to a strategic project aimed at identifying and creating “white space” opportunities through automation. This involves analyzing current workflows, identifying inefficiencies, and supporting the development of automated solutions to streamline planning processes. Hands-On Planning Experience Gain exposure to the end-to-end planning process by assisting with the planning of a subset of products...

About this role The Senior Medical Manager is a part of US Medical Immunology (Lupus and Nephrology), a strategic partner within Biogen, that helps inform medical practice across our therapeutic areas and pipeline to improve meaningful patient outcomes. As a key member of the US Immunology Medical Director office team that reports to the Medical Director, Immunology, the Senior Medical Manager – Lupus will collaborate closely with Medical Operations to coordinate and execute the lupus key medical strategies and tactics. Biogen’s priority is to continue to foster and enable a diverse and inclusive workforce – representing age, gender, sexual identity,...

This position follows a traditional 2-2-3 format from 6a-6P (Day Shift) About This Role The Manufacturing Lead performs and documents daily manufacturing operations in a cGMP environment including operation of process equipment, execution of validation protocols, revising cGMP documents, ensuring compliance to cGMP, as well as maintaining equipment and facilities. This position works closely with shift Supervisor to coordinate critical activities collaboratively and utilizes resources efficiently. This is a key preparatory role for the Manufacturing Supervisor position. The Manufacturing Lead responsibilities include but are not limited to Executes manufacturing processing steps and/or manufacturing support activities, monitoring the process against the...

About This Role As the Head of Drug Safety & Pharmacovigilance (PV) for the West Coast Hub, you will be at the forefront of ensuring the safety and efficacy of our therapies focused on immune-mediated diseases. This pivotal position requires strategic oversight and scientific leadership to maintain the integrity of our global safety surveillance activities. Your role is essential in safeguarding patient well-being and optimizing the benefit-risk profile of our therapies throughout their lifecycle. Reporting directly to the Head of Regulatory & PV, you will spearhead safety science, clinical and post-marketing surveillance, and regulatory safety engagement. You will collaborate closely...

About the Role This application is for a 12-week internship role from June - August 2026. Resume review begins in January 2026. The intern in the Medical Research team will support a project to enhance the management of publication and study results from our portfolio of completed investigator sponsored and Phase 4 research studies. Under the supervision of the Director, Medical Research Process & Governance in the Global Medical Capabilities function, the intern will review completed final study reports and publications to create summaries, prepare reporting, and ensure appropriate tracking in research and publications systems. This project will cover all...

About the Role This application is for a 12-week internship role from June - August 2026. Resume review begins in January 2026. This role is looking for 3 interns. The Biostatistics Department in the Statistical Sciences & Evidence Generation organization provides statistical support across Research and Development. Biostatisticians in the Biostatistics Department collaborate with stakeholders from different disciplines to develop agile and robust clinical development plans and decision frameworks for a portfolio of products encompassing early and late-stage development. They also provide statistical expertise and manage the activities for clinical programs to ensure valid and efficient study designs. What You’ll...

About This Role Pharmacometrics analyses and insight are critical in the development of drug candidates, determination of product viability, and maximization of commercial value at Biogen. As the Associate Director, Pharmacometrics, you will provide pharmacometrics expertise for high-priority clinical development programs and support quantitative decision-making through advanced modeling and simulation. In this role, you will contribute to the pharmacometrics strategy across disease areas and serve as a key scientific resource to program teams and functional partners. You will report to the Head of Clinical Pharmacology, West Coast Hub (WCH) and collaborate closely with cross functional teams to ensure pharmacometrics analyses...

This role operates on a 2 2 3 schedule for Night Shift- 6p-6a. About This Role Our Manufacturing Associates perform processing steps and manufacturing support activities in our Drug Product facility in Research Triangle Park (RTP). These teams are the backbone of our operations – each playing a critical role in delivering our therapies to the patients who need them. Our teams are organized by the steps in the biomanufacturing process that they operate in; including – Parenteral Filling MAs perform these critical steps in a clean environment governed by Current Good Manufacturing Practices (cGMP). What You’ll Do Execute daily...

About This Role The Senior Manager, Scientific & Value Communications role is a part of the US Medical Affairs Team, acting as a strategic partner that helps inform medical practice across our systemic lupus erythematosus (SLE) and cutaneous lupus erythematosus (CLE) asset 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. This individual contributor role supports a lupus pipeline product and reports to the Head of Scientific & Value Communications, US Medical. What...

About This Role Biogen is seeking an accomplished scientific leader to serve as Head of Immunobiology Therapeutic Innovation within the Immunology Research Unit (IRU). This newly created role will define and execute Biogen’s strategy for emerging therapeutic modalities in immunology, driving innovation from early discovery through early development. The successful candidate will play a pivotal role in sourcing and advancing external innovation under Biogen’s Open Innovation model, which prioritizes leveraging the best ideas—internal or external—to accelerate breakthrough science. This includes identifying and assessing new opportunities, leading initial diligence activities, and supporting collaborations with academic institutions, biotech partners, and start-ups. Working...

About This Role We are seeking a highly motivated and accomplished Principal Scientist with deep drug discovery and development experience in diseases with an inflammatory etiology to join our growing Immunology Research Unit in our West Coast Hub, SSF site. The ideal candidate will have a strong background in immunology, cellular and molecular biology and/or a related scientific field and contribute to the discovery and development of novel therapies targeting inflammatory and autoimmune disorders. This role requires a strong foundation in experimental design, data interpretation, and technical leadership, combined with the ability to evaluate external opportunities and contribute to strategic...

About This Role As the Senior Director, Global Regulatory CMC - Drug-Device Combination Products, you will serve as the enterprise regulatory leader for our global device and combination product portfolio. Operating within the Product Delivery Solutions team, you will have end-to-end accountability for defining and executing CMC regulatory strategy across development, licensure, commercialization, and lifecycle management. Your role is crucial in shaping the long-term regulatory posture for device-enabled therapies, ensuring patient supply continuity, and influencing global regulatory policy. Reporting to the VP, Head of Product Delivery Solutions, you will be a core member of both the Product Delivery Solutions Leadership...

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 the Role This application is for a 12-week internship role from June - August 2026. Resume review begins in January 2026. The Clinical Development Group seeks a talented intern to join our team and will be responsible for gathering and analyzing data to support efforts to better understand clinical trial outcomes. Our group evaluates novel therapies for immunology and neurology diseases. What You’ll Do The position requires familiarity with analysis and interpretation of experimental results. The individual will be expected to work collaboratively with team members and groups across Biogen. The project will focus on identifying data sources, gathering...

About This Role Biogen’s West Coast Hub, based in South San Francisco, is specifically focused on transforming the lives of patients with severe immune-mediated diseases by developing novel targeted therapies with outsized clinical impact, faster. To accomplish this, we are seeking top talent to join us on our journey. The Clinical Operations Program Leader (COPL) plays a pivotal role in leading the strategy, planning, and execution of clinical development program operations for Biogen’s Transplant programs. Reporting to the Head of Clinical Operations, West Coast Hub, the COPL serves as a key program-level representative. In this capacity, you will provide advanced...

This position follows a traditional 2-2-3 format from 6a-6P (Day Shift) About This Role The Manufacturing Lead performs and documents daily manufacturing operations in a cGMP environment including operation of process equipment, execution of validation protocols, revising cGMP documents, ensuring compliance to cGMP, as well as maintaining equipment and facilities. This position works closely with shift Supervisor to coordinate critical activities collaboratively and utilizes resources efficiently. This is a key preparatory role for the Manufacturing Supervisor position. The Manufacturing Lead responsibilities include but are not limited to Executes manufacturing processing steps and/or manufacturing support activities, monitoring the process against the...

This role operates on a 2 2 3 schedule for Day Shift- 6a-6p. About This Role Our Manufacturing Associates perform processing steps and manufacturing support activities in our Drug Substance facility in Research Triangle Park (RTP). These teams are the backbone of our operations – each playing a critical role in delivering our therapies to the patients who need them. Our teams are organized by the steps in the biomanufacturing process that they operate in; including – Large Scale Cell Culture MAs perform these critical steps in a clean environment governed by Current Good Manufacturing Practices (cGMP). What You’ll Do...

About This Role The Medical Director will serve as a senior strategic leader, providing expert medical guidance to shape development programs, launch planning, and lifecycle support for lupus —with the goal of improving meaningful patient outcomes. As a key member of Biogen’s Lupus Global Medical Affairs team, you will drive the design and execution of the Global Medical Strategy for CLE in dermatology and strengthen Biogen’s leadership within the global lupus medical community. Biogen is committed to fostering a diverse and inclusive workforce—representing age, gender, sexual identity, race, ethnicity, veterans, and people with disabilities—that reflects the communities we serve and...

About This Role As the Head of Clinical Trial Delivery, you will play a pivotal role in the Leadership Team for Quantitative Sciences & Development Operations (QSDO). You will lead the charge in clinical trial delivery across all Biogen Disease Areas, taking broad responsibility for a diverse portfolio of clinical programs in Neuroscience, Rare Disease, and MS/Immunology therapeutic areas, alongside Real World Evidence. This role is crucial in providing strategic operational leadership to optimize the execution of clinical trials and programs. You will have the opportunity to participate in decision-making bodies and contribute to strategic plans, developing strong relationships with...

About This Role You will join the North American Business Operations & Insights (BIO) team in Omnichannel Excellence, as a critical partner to Biogen’s US marketing teams. You will be accountable for leading End-to-End Content operations in support of our US teams. We are seeking a dynamic AD of Content Operations to design, lead, and scale a US derivative content production and distribution engine — one that delivers high-quality, relevant derivative content at pace, scale, and low cost . This role will sit at the heart of our content ecosystem, transforming how we plan, create, and deploy derivative content. You...

About this Role The Executive Assistant will be a dynamic and self-motivated individual able to provide executive administrative support to the Head of US Nephrology and US Nephrology LT. The right candidate must be flexible, organized, proactive, collaborative, curious, and calm under pressure. Excellent communication, inter-personal and collaboration skills are essential for this role due to interactions across all levels of the organization. Demonstrated experience problem-solving with diplomacy and tact is required. This position also requires a professional demeanor, sense of urgency, the ability to prioritize, and a high level of discretion with the ability to appropriately handle sensitive and...

About the Role This application is for a 6-month student role from July - December 2026 . Resume review begins in January 2026 . Biogen’s Decision & Quality Analytics Innovation (DQAI) team is part of the R esearch D evelopment & M edical (RDM) organization. The vision of the DQAI team is to drive data-driven insights from trusted data , and our team mission is to maximize the quality, efficiency and application of analytics across RDM Portfolio and Quality Management Systems through improved data and metrics management, optimization opportunities, identification of compliance risk, and enhanced business analytics application. Specifically,...

About the Role This application is for a 6-month student role from July - December 202 6 . Resume review begins in January 202 6 . Under direction, the co-op partners with the Manufacturing Sciences team to develop an Assessment of the BOM optimization for consumables, partnering with AAO in process trending for the ASO and OSD facilities, Check Curricula Assignments, and the development of process efficiencies through PF, ASOs and OSD . Must be able to analyze simple issues and align on potential solutions with guidance . What You’ll Do Example projects may include Partners with the Manufacturing...

About the Role This application is for a 6-month student role from July - December 202 6 . Resume review begins in January 202 6 . This role supports the development of oligonucleotide therapeutics by developing innovative analytical technologies . This role will develop and optimize analytical methods on LCMS systems in the lab in Cambridge, MA campus. This role will also support other relevant oligonucleotide studies using various instruments. This position requires adequate knowledge in analytical techniques such as UV, LC and LCMS. What You’ll Do As a co-op, you will work under the guidance of the manager...

About This Role The Executive Administrative Assistant will be a dynamic and self-motivated individual able to provide administrative support and coordination to two Heads of Clinical Development and their team. In addition, the Executive Assistant may also provide support for other members of the Clinical Development Leadership Team and participate in the organization, planning, and execution of activities with other Development administrative and operations staff. The right candidate must be proactive, agile, organized, collaborative, and calm under pressure. Excellent communication, interpersonal and collaboration skills are essential for this role due to interactions with colleagues within the group as well as...

About the Role This application is for a 6-month student role from July - December 202 6 . Resume review begins in January 202 6 . We are seeking a motivated co-op to join the Analytical Development Biologics group in Cambridge, MA , and contribute to our mission to develop advanced analytical methods to support portfolios and drive innovation. What You’ll Do As a co-op, you will develop and optimize LC-MS based methods to characterize and quantify host cell proteins in biologics and execute the developed LC-MS HCP method to provide decision-enabling information to the process development and other...

About the Role This application is for a 6-month student role from July - December 202 6 . Resume review begins in January 202 6 . Biogen’s Research Triangle Park (RTP) site is seeking a motivated Manufacturing Engineer Intern to support large scale manufacturing purification operations. In this role, the intern will work closely with manufacturing engineers and cross-functional teams to improve process reliability, support day-to-day production activities, and contribute to continuous improvement initiatives in a cGMP biopharmaceutical environment. Key responsibilities may include data collection and analysis, equipment performance monitoring, troubleshooting support, documentation updates, and assisting with small-scale studies or...

About This Role The Regional Sales Director, reporting into West Divisional General Manager, provides leadership and strategic direction to Territory Business Managers to achieve performance objectives within our Specialty Franchise with focus on Multiple Sclerosis. This is accomplished through strong leadership competencies, effective coaching, utilization of resources and strong collaboration with other divisions or disciplines within Biogen and external business partners. The Regional Director will cover the Pacific Northwest area What You’ll Do Achieve Region goals for the Biogen MS portfolio, including driving demand, retaining appropriate patients in therapy, and managing region budget. Leverage coaching model to maximize the development...

About the Role This application is for a 12-week internship role from June - August 2026. Resume review begins in January 2026. The Manufacturing Technical Operations (MTO) Team supports the Parenteral Facility Manufacturing Department. The group consists of specialists who serve the PF as process experts by managing various documentation and compliance needs of the Manufacturing team. Additionally, this team introduces new products to the facility and serve as project managers for continuous improvement projects. What You’ll Do As an intern in this department, you will gain hands-on exposure to biotech manufacturing processes and learn how they are designed, documented,...

About the Role This application is for a 6-month student role from July - December 202 6 . Resume review begins in January 202 6 . The RTP Pharma site supports two sterile filling lines in the Parenteral Fill (PF) facility, a small-scale filling line, Antisense Oligonucleotide (ASO) Manufacturing Areas , and an Oral Solid Dose (OSD) Manufacturing Area. As a Co-Op in Quality Engineering, the successful candidate will help ensure that Quality systems supporting facility, equipment, automation, and utilities remain in compliance with Biogen and industry cGMP standards. These activities would include support of facility and equipment controls...

About the Role This application is for a 12-week internship role from June - August 202 6 . Resume review begins in January 202 6 . The Q uality C ontrol (QC) Raw Materials team is responsible for ensuring that all materials needed within manufacturing are inspected, sampled, tested, and released to meet manufacturing timelines . This team works closely with Materials Management and Planning to meet these commitments . As an intern within this team, you can expect to learn how materials are introduced into the facility and how the quality control team ensures that these materials meet...

About the Role This application is for a 6-month student role from July - December 202 6 . Resume review begins in January 202 6 . The Material s Planning & Supply Chain Intern supports operational efficiency and sustainability initiatives within Biogen’s manufacturing network. This role is responsible for evaluating existing material inventories and determining their continued relevance to current manufacturing processes. This role contributes to cross-functional efforts to improve material flow, optimize inventory practices, and propose sustainable alternatives. What You’ll Do Assess material content in recycling containers and determine alignment with existing and future manufacturing process requirements. Perform data...

About the Role This application is for a 6-month student role from July - December 202 6 . Resume review begins in January 202 6 . We are seeking a motivated co-op to join our Small Molecule Formulation Development team. This position offers hands-on experience in advanced drug delivery technologies aimed at improving oral bioavailability. The co- op will contribute to a project that integrates amorphous solid dispersion (ASD) and lipid-based excipients within an immediate-release (IR) tablet and/or capsule platform. The ideal candidate will bring a strong foundation in solid dispersion and lipid-based formulations, along with an understanding of...

About the Role This application is for a 6-month student role from J u ly - December 202 6 . Resume review begins in January 202 6 . Biogen is seeking a highly motivated co-op to join the Biologic Drug Product Development team . This co-op position offers a n exciting opportunity to contribute to the In-vitro evaluation of subcutaneous (SC) monoclonal antibod y ( mAb ) formulations . The co-op will perform experiment s using in-vitro to ol s to evaluate formulation performance and stability . The candidate will also conduct literature reviews on approved antibody products and contribute...

About the Role This application is for a 6-month student role from July - December 202 6 . Resume review begins in January 202 6 . As a member of the Asset Development & Portfolio Management team (ADPM), the Portfolio Planning Systems Analyst works with operations staff to improve planning practices (program scheduling, employee resource forecasting, and cost forecasting) through data-based insights and the development of effective performance measures. The role entails collecting and analyzing complex data from multiple systems, distilling results into clear insights about process gaps and opportunities, and developing effective communications to motivate action toward better planning...

Research Project Management Lead (Associate Director) About This Role We are seeking an experienced project management professional to drive strategic and operational excellence within the Research business unit. In this role, you will lead the translation of strategy into execution for teams advancing Research portfolio programs. Creating project plans and managing activities in close partnership with project leaders and functional experts, you will ensure that milestones, timelines, and decision points are achieved, that program risks are objectively assessed and proactively managed, and that program decisions are made in an aligned, transparent, and data-driven manner. Your work will span both internal...

About This Role The Head of Research Project and Portfolio Management will lead project planning, execution, and portfolio management practices to optimize the delivery of Biogen’s Research portfolio, spanning from early stage discovery through IND filing. This role is accountable for shaping portfolio strategy and optimization by creating a common understanding of the state of the Research portfolio including value, risks, and upcoming inflection points; by driving clarity and alignment on key imperatives to progress and evolve the portfolio; and by ensuring that portfolio priorities and resourcing align to organizational objectives. This role will also build and scale a Research...

About the Role This application is for a 6-month student role from July - December 2026. Resume review begins in January 2026. Work within the Pharma Drug Substance organization engaged in laboratory activities supporting the development of small molecule therapeutic products, manufacturing processes or new technologies. What You’ll Do As a co-op you will gain hands-on experience in process development of small molecule pharmaceuticals. You will work closely with the Small Molecule Chemistry Development team. Under general supervision, you will design and execute chemical reactions in the laboratory aimed at gaining process understanding and making process improvements to a manufacturing...

About This Role Biogen is preparing to launch an asset currently in development across multiple Lupus indications. As the Director, Global Launch Excellence and Commercialization for Lupus, you will collaborate with and guide cross-functional teams through key planning milestones to deliver impactful launch plans providing exceptional program management and developing launch frameworks that set the stage for future launches at Biogen. You will be accountable for leading cross-functional and cross-regional matrix teams to develop and execute robust launch plans, provide launch progress updates for c-suite stakeholders, build and enhance organizational capabilities for launch via new methods, tools; and maximize launch...

About This Role The Director, Global Competitive Intelligence (CI) for Immunology leads Biogen’s CI strategy and execution for the immunology portfolio. This role delivers actionable insights to inform pipeline development, clinical positioning, and commercial strategy. The role establishes robust monitoring frameworks, synthesizes complex data into clear recommendations, and partners cross-functionally to embed CI into decision-making processes while ensuring compliance with ethical and legal standards. What You’ll Do Develop and maintain a strategic framework for tracking competitor activities across portfolios and geographies. Partner with senior leaders and Product Development & Commercialization (PDC) teams to embed CI into brand, portfolio, and enterprise...

About This Role The purpose of this position is to be the patient facing expert on the Rare Disease patient journey and the liaison for all Biogen team members involved in the process. The Family Access Manager (FAM) is responsible for engaging cross functional stakeholders on the next steps to support appropriate patients getting started and staying on rare disease therapies. The FAM will get to the root of any logistical and/or non-clinical issues impacting treatment initiation and ongoing therapy. They can identify the point person, tools, or resources to resolve the issue (Account Executive, Market Access & Reimbursement, and/or...

Development Asset Lead, Director Development About This Role As a Development Asset Lead (DAL), you will play a pivotal role in leading the strategic development and execution of one or more preclinical or clinical stage portfolio assets within our Development team. This full-time leadership position requires you to craft and implement an integrated asset plan (IAP) that maximizes value creation and delivery. You will ensure that all functional voices are represented and that business considerations of time, risk, and value are integrated seamlessly into the planning and execution phases. This role is crucial to our business, as you will be...

About this role The Senior Analyst, Statistical Programming leads and oversees statistical programming activities both internally and externally through vendors in the application of data standards, production of analysis datasets, analysis dataset specifications, tables, listings, figures, electronic submission components, and ad hoc analyses. You will partner with Biostatistics to deliver high quality, submission ready statistical outputs with some supervisions. You are responsible for providing input to the Portfolio Lead (PL) on overall study timeline, monitoring and meeting agreed upon study milestones, escalating issues as needed to their PL counterpart and estimating resources needs. You will lead a study team of...

About This Role Biogen’s two-year PhD fellowship in Worldwide Medical (WWM) is an exceptional opportunity for recent doctoral graduates to immerse themselves in the dynamic world of Medical Affairs and the broader pharmaceutical industry. As a fellow, you will engage in a comprehensive, hands-on learning experience that provides an accelerated introduction to a career in medical affairs within a pioneering biotech environment. In the first year, you will undertake four distinct, 3-month rotational experiences across various functional areas within Worldwide Medical, with an additional opportunity to select a rotation outside of medical. This exposure will deepen your understanding of our...

About This Role The Senior Manager, Global Insights will partner with the Global Insights Leads for Nephrology in delivering high-quality insights and forecasting to inform strategic and operational decisions across the nephrology portfolio. This role will focus on generating actionable insights from multiple data sources, supporting market research, competitive intelligence, and forecasting activities. The individual will collaborate closely with cross-functional teams and global/local stakeholders to ensure insights are effectively translated into business strategies. The position requires strong analytical skills, strategic thinking, and the ability to synthesize complex data into clear recommendations. What You’ll Do Analyze and interpret diverse data sources,...

About This Role This position is on a 12-hour rotation, Red Night shift on a 2, 2, 3 schedule This position is responsible for the supervision of manufacturing of clinical and commercial products under GMP conditions. The incumbent will supervise Manufacturing Associates on a Night shift; schedules shift tasks; ensures GMP compliance and safety; drafts and reviews manufacturing documents; troubleshoots; and coordinates with other departments. What You'll Do Supervises Manufacturing Associates – observing/instructing, coaching, leading and developing staff. Identifies technical/non-technical development gaps and implements applicable plans/objectives. Performs manufacturing activities per cGMPs, ensuring that reports are fully trained on a given...

About this role The (Sr) Medical Science Liaison role is a part of US Medical Affairs, a strategic partner within Biogen, that helps inform medical practice across our therapeutic areas and pipeline to improve meaningful patient outcomes. The (Sr) Medical Science Liaison enables critical stakeholder engagement with Key Medical Experts (KMEs) and other healthcare professionals (HCPs) so they understand the clinical and scientific narrative for Biogen’s therapies. Biogen’s priority is to continue to foster and enable a diverse and inclusive workforce – representing age, gender, sexual identity, race, ethnicity, Veterans, and people with disabilities – that reflects the communities where...

About This Role As the Director of Market Access Strategy, you will play a role in shaping and influencing the US market access strategy for Biogen’s Alzheimer's portfolio. Your primary focus will be on Alzheimer’s treatments, including both IV and subcutaneous maintenance and initiation, in collaboration with our alliance partner. This position serves as the central conduit across Biogen's Market Access & Reimbursement (MA&R) team and the Alzheimer’s commercial team, as well as alliance market access stakeholders. Your efforts will ensure aligned strategy, smooth execution, and measurable outcomes. What You’ll Do Oversee/shape access strategy development for Alzheimer (IV & Sub‑Q)...

This role operates on a 2 2 3 schedule for Day Shift- 6a-6p. About This Role Our Manufacturing Associates perform processing steps and manufacturing support activities in our Drug Product facility in Research Triangle Park (RTP). These teams are the backbone of our operations – each playing a critical role in delivering our therapies to the patients who need them. Our teams are organized by the steps in the biomanufacturing process that they operate in; including – Parenteral Filling MAs perform these critical steps in a clean environment governed by Current Good Manufacturing Practices (cGMP). What You’ll Do Execute daily...

About the Role This application is for a 12-week internship role from June - August 202 6 . Resume review begins in January 202 6 . The QC Microbiology team is responsible for ensuring the safety of our products by checking for microbial contamination . The team samples surface and air sites in manufacturing areas , performs facility water testing and tests in-process and final drug product samples . We e nsure adherence to Good Manufacturing Practices (GMP) and regulatory guidelines (FDA, EMA, etc.) for microbiological quality . Data generated from the lab is a nalyze d to detect...

The Principal Analyst, Statistical Programming leads and oversees statistical programming activities of internally and externally through vendors in the application of data standards, production of analysis datasets, analysis dataset specifications, tables, listings, figures, electronic submission components (define.xml and XPTs), and ad hoc analyses. He/she partners with Biostatistics to deliver high quality, submission ready statistical outputs. This person is also responsible for providing input to the Development Unit Lead (DU Lead) on overall study timeline, monitoring and meeting agreed upon study milestones, escalating issues as needed to their DM counterpart and estimating resources needs. He/she leads a study team of statistical...

About the Role This application is for a 6-month student role from July - December 202 6 . Resume review begins in January 202 6 . The QC Microbiology team is responsible for ensuring the safety of our products by checking for microbial contamination . The team samples surface and air sites in manufacturing areas , performs facility water testing and tests in-process and final drug product samples . We e nsure adherence to Good Manufacturing Practices (GMP) and regulatory guidelines (FDA, EMA, etc.) for microbiological quality . Data generated from the lab is a nalyze d to detect...

About the Role The Associate Medical Director, Neuropsychiatry (NP) is a key member of the U.S. Medical Affairs team, supporting development and execution of the medical strategy for Biogen’s Neuropsychiatry therapeutic area. Reporting to the Medical Director within the U.S. Neuropsychiatry Medical Director’s Office, this role focuses on generating high-quality clinical and real-world evidence to inform medical practice, support product strategy, and improve patient outcomes. Key Responsibilities Support the Medical Director in the development and execution of the U.S. real-world evidence (RWE) strategy. Support the design, contracting, execution, and interpretation of clinical trials and RWE studies in neuropsychiatry, including identification...

This is a remote-based position, candidate must be located within the USA About This Role Ready to make a global impact? Join us as a Senior Manager in Global Labeling and become a key player in shaping how life-changing therapies reach patients worldwide. This is more than a role – it’s an opportunity to lead, collaborate across cultures, and grow your career while ensuring compliance and excellence in every detail. If you’re passionate about precision, innovation, and working with diverse teams to deliver results that matter, we’d love to meet you. As a Senior Manager in Global Labeling, you will...