Biogen Job Trends

About This Role Corporate Development leads the establishment of Biogen’s corporate strategy and is responsible for the identification, assessment and negotiation of external opportunities to augment Biogen’s pipeline, as well as integration of acquired companies and management of relationships with Biogen’s partners. The Search & Evaluation Director will be contributing to the search and evaluation process to proactively identify and scientifically/technically evaluate external growth opportunities for inbound partnering (e.g., collaborations, licensing, and M&A) in the Neuroscience, Immunology and/or Rear Disease therapeutic areas for Biogen with potential for growth. What You’ll Do Work closely with Corporate Strategy and R&D Leadership to...

About This Role The Director, Global Insights Lead for Alzheimer's Disease & Dementia is a pivotal role that influences the strategic direction of our business and enhances brand success. Embedded within the Product Development and Commercialization team, you will focus on the Dementia pipeline, guiding strategic initiatives and competitive positioning through data-driven insights. You will partner with key stakeholders to uncover opportunities by deeply understanding customer groups, market dynamics, and competitive landscapes. By leveraging large datasets and advanced analytics, you will identify patterns, trends, and correlations that inform decisions and support insights generation requirements for both pre-launch and lifecycle management...

About This Role Corporate Development leads the establishment of Biogen’s corporate strategy and is responsible for the identification, assessment and negotiation of external opportunities to augment Biogen’s pipeline, as well as integration of acquired companies and management of relationships with Biogen’s partners. Reporting to the Head of Business Development/M&A, the Business Development Transactions Sr Dir ector w ill be responsible for the business evaluation and execution of impactful business development opportunities across therapeutic areas , asset stages, and deal types including R&D or commercial partnerships, licenses, collaborations , and/or acquisitions that fit within the overall corporate strategy, business plan and...

About This Role Corporate Development leads the establishment of Biogen’s corporate strategy and is responsible for the identification, assessment and negotiation of external opportunities to augment Biogen’s pipeline, as well as integration of acquired companies and management of relationships with Biogen’s partners. Reporting to the Head of New Ventures, the New Ventures Senior Director will be leading the identification and evaluation of external growth opportunities to build an externalized portfolio of research and early clinical stage assets by utilizing alternative deal constructs to incubate and capture breakthrough innovation. Additionally, this individual will be responsible for managing and operationalizing assets in...

About This Role Biogen is searching for a collaborative, strategic, and results-oriented Neurology Account Specialist (NAS) that will provide support for the launch of a medication for the treatment of MCI and Alzheimer’s Disease. In this field-based role, you’ll be responsible for developing and maintaining critical relationships with neurologists and other allied health professionals and support staff. Additionally, the role will leverage account management competencies to increase screening of MCI and Alzheimer’s Disease, support referrals to treating neurologists and drive focused initiatives that impact Alzheimer’s treatment pathways in affiliated health groups and systems. The NAS is responsible for developing and...

About This Role The Associate Director Head of Clinical Trial Transparency (CTT) Operations leads and oversees all CTT activities, ensuring compliance with global regulations and Biogen policies for clinical trial registration and results disclosure. This role manages CTT resources, driving the function's performance and results. Key goals include aligning public information needs, regulatory requirements, and industry commitments across the portfolio, and maintaining audit and inspection readiness. The Head of CTT Operations also acts as the business unit representative for the CTT vendor, overseeing compliance, contract terms, process improvement, and budget. This position, which contributes to the functional strategy and reports...

About This Role As part of our Automation & MES team, the Engineer II, Automation plays a pivotal role in supporting Biogen's RTP Bio site's operational and project goals. This position primarily focuses on maintaining and troubleshooting process control system hardware and software, including DeltaV DCS and Syncade MES, for biopharmaceutical manufacturing. You'll be responsible for creating software design specifications, implementing new control strategies, authoring recipes, and developing software test protocols for new products and processes. Additionally, you'll perform Responsible Engineering duties, such as reviewing validation protocols and creating Change Controls for system modifications. This role requires participation in an...

About this role The Medical Science Liaison / Senior Medical Science Liaison (MSL) 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 MSL 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...

As a Senior 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 contribute to...

About This Role The Senior QA Associate II in the Quality Systems organization is responsible for understanding quality systems, contributing to oversight of quality systems, and maintaining GMP and laboratory activities at the Biogen RTP facility. They should be proficient in their understanding of the quality systems and apply that knowledge in coaching and continuous improvement. The primary responsibilities of the Senior QA Associate II in the Quality Systems team include quality compliance for managing Drug Substance (Bio) Quality Systems, responsible as the Business Process Owner for the document issuance process, authoring Site Reports (Site Management Review Report), change control...

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...

Sr. Supervisor This position is on a 12-hour rotation, Day 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; 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. Provides on the floor support with manufacturing associate(s). · Performs manufacturing activities per cGMP, ensuring that reports are fully...

About This Role The Senior Manager, Operational Reporting and Analytics (OpRA) will be responsible for the design development and ongoing support of the reporting infrastructure(s) to support the Safety and Benefit Risks (SABR) and Global Regulatory Affairs (GRA) teams in their transition to Veeva. This role will be looked upon to provide expertise and guidance to the OpRA team on best practices for data integrations using the latest database software and related technologies (Snowflake). This position reports to the Director of TADI Operational Reporting and Analytics. (TADI = Technology, Analytics, Data, and Insights) What You’ll Do Provide expertise supporting reporting...

About This Role The Medical Director, Rare Disease role is a part of North America (US) Medical Affairs, 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 Rare Disease Medical Director’s office team reporting to the USMA Rare Disease Head, the Medical Director for SMA (Spinal Muscular Atrophy) is medically accountable for supporting the development and implementation of the US Medical Strategy for Biogen’s SMA therapeutic area commercialized products, pipeline, and related assets. Biogen’s priority is to continue to foster and...

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 This Role As the Associate Director of IT Financial Management within IT Management Operations (ITMO), you will take the helm in guiding the financial strategies of our IT organization. Reporting to the Head of IT Management Operations, you will oversee IT financial planning, including annual operating plans, quarterly forecasts, and continuous improvement tracking. Your role is pivotal in driving the financial performance and efficiency of our IT functions. By managing key metrics and collaborating with Finance, you will ensure seamless financial operations that align with our organizational goals. This position requires a strategic mindset and a keen understanding of...

This is a full time, on-site position About This Role This position will support our drug substance (Bio) site at our Research Triangle Park NC facility. The primary responsibilities of the Senior Associate III include quality compliance for managing site inspections, completing regulatory requests for partner and Biogen products, authoring Site Reports (Site Management Review Report and Site Master File), change control support, and the review and approval of site-specific GMP documents (Work Instructions, Master Production Records, and Solution Records) for compliance to applicable regulatory and corporate guidance documents, and consistency with business source documentation. What You’ll Do Management of...

About This Role Biogen is seeking an experienced leader to serve as the Director of Environmental, Health, and Safety (EHS) for our RTP Bio site. In this pivotal role, you will lead the EHS function supporting the management of all EHS aspects of RTP Operations (Drug Product, LSM, OSD, 2K and Patient Services), to include ensuring compliance with all legal and other requirement, identification and mitigation of EHS risks, and management and mitigation of our environmental footprint for 5000 Davis Drive. Your strategic oversight will be critical to implementing Biogen's EHS Management System effectively at the site level, ensuring alignment...

About This Role As a Medical Director, Clinical Development – Immunology, you will be an integral member of the Immunology Therapeutic Area within the Clinical Development Organization. In this dynamic role, you will play a critical part in shaping and advancing clinical programs, particularly in the lupus and autoimmune disease space. Reporting to the Executive Director, you will be instrumental in crafting the clinical development strategy and leading the execution of complex clinical trials. Your leadership will not only impact the direction of clinical studies but also contribute to the broader objectives of the organization. Your expertise will be pivotal...

About this Role As an Executive Director, Development Asset Lead (DAL) , you will serve as a senior leader within Biogen’s Development organization. You’ll manage and mentor a subset of Development Asset Leads (DALs), who are responsible for leading cross-functional development teams for preclinical and clinical-stage assets across the portfolio. This role requires strategic leadership, deep knowledge of drug development, and the ability to drive high-impact decisions in a complex matrixed environment. You may also serve directly as a DAL on one or more high-priority assets, accountable for the creation and execution of integrated asset plans (IAPs) that guide program...

About This Role As a Senior OSI Engineer, you will take charge of leading efforts within the Pharmaceutical Operations & Technology (PO&T) division to identify and eliminate waste, streamline processes, and enhance productivity across the organization. Your role will involve a deep dive into Bio-Pharmaceutical operations, leveraging your extensive experience in Manufacturing, Supply Chain, Quality, Engineering, or Product Development. Key responsibilities include utilizing your expertise in continuous improvement (Lean Six Sigma) to champion change at the operational level. You will analyze current processes, pinpoint areas for improvement, and develop sustainable solutions to optimize performance. Collaborating with cross-functional teams, you will...

About This Role This is a full time, on-site position with M-F business hours The Sr Associate I, Quality Assurance 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 Sr Associate I QA has working knowledge of GxP regulations and adheres to all regulatory licenses and regulations as well as internal SOPs. The Sr Associate I QA identifies and resolves issues through...

About This Role As the Senior Director of Medical Affairs Statistics, you will play a pivotal role in leading a dynamic team focused on evidence generation and health technology assessment. This position is critical to ensuring the development and dissemination of scientific evidence of clinical outcomes and product value for marketplace stakeholders. With your expertise, you will impact evidence strategy and oversee analytics which contribute directly to our organization’s success. This leadership role offers an exceptional opportunity to collaborate across functions, mentor a talented team, and make meaningful contributions to patient outcomes and healthcare decision-making. What You’ll Do Lead the...

About This Role Pharmacometric analyses and insight are critical in the development of drug candidates, determination of product viability, and maximization of commercial value at Biogen. As the Director, Pharmacometrics you have responsibility for high priority clinical development assets providing guidance on and executing advanced modeling strategies. You contribute to the Pharmacometrics group strategy across disease areas being a respected and visible leader on Pharmacometric issues for program teams and across the functional organization. This Role reports to the Head of Pharmacometrics. The Director, Pharmacometrics collaborates closely with Clinical Pharmacology advising and mentoring on advanced pharmacology models. What You’ll Do...

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. About This Role The Toxicology Lead, West Coast Hub role will report to the Head of Clinical Pharmacology, WCH with matrixed reporting to the Head of Discovery Toxicology and/or the Head of Development Toxicology. The primary responsibilities of this position are to provide strategic nonclinical safety expertise and representation for clinical development programs from...

About This Role Biogen is seeking a highly experienced and proven IAM Solutions Engineer with deep expertise in Identity and Access Management (IAM), specializing in Privileged Access Management (PAM) and hands-on CyberArk solution engineering. This role demands a strong understanding of directory services, authentication, and authorization systems. As a Sr. Manager, IAM Solutions Engineer, you will be instrumental in the end-to-end design, implementation, and optimization of critical PAM solutions, providing advanced technical leadership, mentoring, and expert-level (L4) support. Your work will directly ensure Biogen’s identity services remain secure, compliant, and aligned with cutting-edge PAM best practices and solutions architecture principles....

About This Role Oversee the implementation and ongoing maturation of processes supporting preclinical portfolio prioritization and differential resourcing of programs within the Research pipeline. Leadership and thought partnership for the implementation of risk identification and management frameworks for the Research portfolio and programs (e.g. heat maps, Chain of Translatability, preclinical risk register), working with stakeholders to ensure consistent use to support team planning and governance decision making. Partner with the governance operations function in SPOQ to refine the preclinical governance operating model and ensure consistent use of portfolio management tools in governance decision-making. Create and update preclinical portfolio summaries based...

About This Role As the Global Trade Compliance Operations Specialist, you will play a pivotal role in ensuring efficient and compliant cross-border trade activities for Biogen. You will be responsible for managing day-to-day import/export compliance operations, as well as Foreign Trade Zone (FTZ) Customs requirements, ensuring compliance with international trade laws. Acting as a key liaison among internal teams, customs brokers, government agencies, and other stakeholders, you will streamline import/export clearance by U.S., and Canada Customs, as well as other government agencies proactively. Additionally, you will serve as the subject matter expert for the global trade management system (GTM), providing...