Biogen

Director

• Define and operationalize the Control Tower remit, focusing on business-critical questions and success factors
• Coordinate with internal and customer-facing stakeholders to identify market shifts and implement actions supporting Therapeutic Area strategic goals
• Structure and manage the Insights to Action process, emphasizing insight gathering, dissemination, and feedback loops
• Design and implement processes for systemic gathering, structuring, and dissemination of key insights
• Regularly assess and adjust processes to meet business needs in an agile manner
• Serve as a connector between brand teams and functional support areas for actionable tactics and solutions
• Implement and facilitate collaboration forums using agile best practices for Control Tower operations
• Coordinate dynamically between customer-facing and internal business support teams
• Integrate market responses and insights to guide strategic decisions and performance monitoring
• Recommend resource redeployment based on continuous learning and brand performance monitoring
• Partner with analytics teams to interpret data into actionable insights
• Prepare and present findings to stakeholders, translating insights into business strategies
• Monitor performance by tracking business outcomes and field activities
• Schedule and facilitate meetings to ensure alignment on key discussion topics and insights
• Report directly to the BIO Head of the Portfolio Strategy, Operations, and Innovation
• Shape and manage the LEQEMBI Control Tower cross-functional team and establish processes scalable across brand teams

Director, Enterprise Insights and Analytics

Medical Science Liaison

• Serve as a credible medical/scientific expert engaging Key Medical Experts and healthcare professionals on disease states and Biogen therapies.
• Build deep, strategic, long-term relationships with internal and external stakeholders.
• Act as a responsive, solutions-driven partner to leaders in the medical community.
• Engage in projects and initiatives aligned to US Medical strategy, objectives, and tactics.
• Deliver against KME engagement plans in collaboration with field and non-field colleagues.
• Navigate medical resources at healthcare offices.
• Capture and report KME/HCP medical insights using Veeva.
• Meet qualitative and quantitative medical excellence goals, standards, and measurements.
• Help inform medical and clinical strategies and support improved patient outcomes.

Senior Medical Science Liaison, Lupus

General

• Contribute to the development and refinement of mechanistic Quantitative Systems Pharmacology (QSP) models supporting drug discovery and development programs
• Explore and evaluate AI and machine learning approaches to enhance and accelerate QSP modeling workflows
• Perform Model-Based Meta-Analyses (MBMA) to generate quantitative evidence informing portfolio strategy and drug development decisions
• Analyze, integrate, and interpret preclinical and clinical data supporting model development and decision-making
• Learn and implement industry-standard data handling and modeling rules
• Prepare internal presentations on work progress on an ongoing basis
• Prepare external poster and manuscript publications when applicable
• Support additional Clinical Pharmacology & Pharmacometrics team tasks as needed

Co-op, Clinical Pharmacology & Pharmacometrics

Human Resources

• Lead an enterprise Procurement team responsible for category strategy, sourcing execution, supplier relationship management, and value delivery across Human Resources and Professional Services spend
• Provide people leadership, coaching, prioritization, and direction to three direct reports and cross-functional category teams
• Lead complex sourcing, negotiation, and contracting strategies, including RFx development, supplier selection, commercial modeling, and negotiation planning
• Set category priorities, remove execution roadblocks, and align sourcing strategies with stakeholder roadmaps and enterprise Procurement priorities
• Facilitate stakeholder alignment, shape demand, lead sourcing events, and coordinate supplier selection, negotiation, and contracting decisions
• Build trusted senior stakeholder relationships and identify value creation opportunities using spend, supplier, market, and demand insights
• Establish and manage strategic supplier relationships through business reviews, performance scorecards, issue resolution, innovation roadmaps, and risk mitigation
• Determine negotiation strategy, supplier segmentation approach, and recommended sourcing models
• Approve team operating cadence, category performance reporting, stakeholder business review content, supplier performance actions, and continuous improvement priorities
• Promote preferred supplier usage, guided buying, catalogs, contract compliance, and efficient buying channels in partnership with Procurement Operations
• Deliver sustainable value through stakeholder experience, supplier governance, risk reduction, responsible sourcing, process efficiency, and innovation

Associate Director, Human Resources – Professional Services Category

Data Scientist

• Collaborate with data scientists and stakeholders to define analytical questions and translate business or scientific needs into data-driven solutions
• Prepare, clean, integrate, and analyze structured and unstructured data from regulatory, R&D quality/compliance, drug safety and/or non-clinical safety sources
• Create dashboards, visualizations, user interfaces, and/or reports that enable data-driven decision making for technical and non-technical audiences
• Research emerging applications of artificial intelligence, machine learning, natural language processing, and advanced analytics in pharmaceutical research and development
• Contribute to reusable data pipelines, code libraries, model documentation, and analytical workflows promoting quality, transparency, scalability, and reproducibility
• Present findings, recommendations, and technical approaches to project teams and stakeholders
• Build LLM chatbots to search unstructured data repositories for answers to regulatory authority queries
• Contribute to human-in-the-loop content and document generation
• Build agents that can interrogate processes like an auditor or inspector
• Develop SOP/guidance to ensure quality and oversight of AI

Co-op, Data Science

• Collaborate with data scientists, portfolio analysts, and subject matter experts to develop and deploy innovative AI and analytics solutions
• Design and implement machine learning, predictive analytics, and decision-support models for portfolio and operational challenges
• Develop interactive dashboards, reporting tools, and data products that translate complex data into actionable insights
• Research and evaluate emerging AI, machine learning, and agentic AI technologies for pharmaceutical R&D
• Partner with Development, Portfolio Management, and Operations stakeholders to understand business needs and deliver scalable solutions
• Contribute to the design and maintenance of data pipelines, AI platforms, and software products supporting enterprise decision-making
• Promote responsible AI practices, model transparency, and continuous learning through experimentation and innovation
• Build AI agents for portfolio reporting, risk identification, and data reconciliation workflows
• Develop predictive and prescriptive analytics for portfolio prioritization and strategic planning
• Develop scalable data pipelines and ETL processes integrating enterprise platform data
• Support the design, optimization, and governance of Biogen’s Snowflake-based data ecosystem
• Create machine learning models and decision-support tools for resource forecasting, quality analytics, and operational intelligence
• Develop Project FORWARD capabilities connecting data, AI, and workflow automation for portfolio management

Co-op, Data Science, AI Innovation

Clinical Research

• Manage day-to-day execution and coordination of clinical trials for Class III medical devices
• Track study activities, timelines, deliverables, and operational issues with cross-functional team members
• Coordinate with study sites, CROs, and external vendors to ensure protocol-required activities meet timelines and quality expectations
• Monitor study progress and operational metrics, identifying risks and issues affecting timelines and data quality
• Support vendor oversight and site management by reviewing performance and operational quality concerns
• Collaborate with Safety, Regulatory, Quality, and Data Management teams
• Assist with documentation, vendor oversight activities, and site management processes
• Facilitate communication among internal team members, CROs, and sites
• Support regulatory submissions, protocol amendments, and safety reporting workflows
• Organize and track follow-up activities such as action item logs and issue trackers

Clinical Trial Manager, Class III Medical Devices

Analyst

• Perform general ledger operations for Biogen’s Affiliates, including cash and treasury reconciliations and accounts receivable transactions
• Manage fixed asset activity, payroll, prepayments, and accruals
• Record revenue and expenses
• Calculate and post journal entries
• Report PnL, BS, and other schedules accurately and timely
• Run PA reports and prepare VAT data and CIT templates
• Prepare balance sheet reconciliations
• Conduct monthly and quarterly analyses
• Collaborate with consultants on statutory financial statement preparations
• Provide data and explanations for internal and external audit inquiries

Senior Analyst, GBS Record to Report

Manager

• Manage continuous improvement projects related to business and technical process improvements to enhance the usability, adoption, and satisfaction with Veeva CRM
• Lead cross functional projects to assist in the development, deployment, and adoption of new field technology and enablement platforms for the US Commercial field teams
• Ensure appropriate field technology training is conducted with new employees
• Identify training gaps with existing technology through in-depth analysis
• Ensure support functions are knowledgeable on field technology capabilities
• Manage and oversee IT resources, particularly the field service desk, to ensure issues are addressed quickly and correctly
• Create comprehensive reports and interpret underlying data to provide accurate and actionable insights
• Assist with troubleshooting large technology issues by managing without authority
• Maintain training content and measure field-user satisfaction and utilization with Veeva CRM

Manager, Field Technology

Operations

• Provide direct line management for assigned Clinical Country & Site Leads, Site Managers, and Site Feasibility team members
• Conduct regular 1:1s, objective setting, performance reviews, development planning, coaching, recognition, and performance or conduct management
• Build team capability and succession strength through onboarding, mentoring, feedback, development assignments, and career planning
• Allocate CCSLs across country and study portfolios based on business priorities, capability, capacity, and development needs
• Monitor workload and recommend resourcing or prioritization changes when risks or imbalances arise
• Oversee the quality and consistency of country and site intelligence, investigator engagement, country and site strategy input, Sponsor Oversight Visits, CRO/FSP oversight, issue escalation, and audit or inspection support
• Guide operational insights into recommendations for protocol planning, country and site selection, enrollment assumptions, and study execution
• Serve as an escalation and decision-support point for country, site, investigator, data integrity, patient safety, quality, and partner-performance concerns
• Partner with CMLs, Site Managers, study teams, affiliates, CROs, and FSP organizations to clarify roles and resolve delivery barriers
• Track team objectives, operational performance, capability needs, and portfolio risks
• Provide updates and recommendations to CSO leadership and support workforce, resource, and budget planning
• Lead or contribute to CSO operating-model, process-improvement, and change initiatives
• Represent CSO in selected cross-functional forums

Associate Director, Country & Site Operations

Research Analyst

• Set strategy for Biogen China study execution and publication
• Collaborate with medical managers on data generation for medical-initiated and investigator-initiated studies
• Develop and update local affiliate SOPs, protocols, feasibility assessments, and conduct Phase IV, IIT, and other studies
• Manage study operations and accountability according to protocols, contracts, GCP, SOPs, and applicable laws
• Establish and maintain China study SOPs, handbooks, and clinical operations guidance aligned with global SOPs
• Develop protocols for Biogen China-sponsored studies with TA Medical
• Serve as primary contact for China data generation communications and collaborate with global and regional functions
• Support milestone achievement and manage study issues with cross-functional Biogen teams
• Manage study submissions, governance processes, and the MARS study tracking system
• Select and manage vendors, ensure study quality, and provide vendor training and materials
• Coordinate vendor contracts and payments for post-marketing research activities
• Identify study quality risks and implement corrective and preventive action plans
• Manage site quality, supervise project CRAs, and monitor deliverables
• Lead study audit preparation
• Define publication objectives, strategy, and timelines
• Coordinate local study data analysis with global medical and publication resources
• Manage publication-related processes and projects with global publication teams and local TA
• Ensure local vendors complete data analysis accurately and on time
• Select publication vendors and ensure compliance with Biogen requirements and standards
• Align local publication SOPs with applicable global SOPs

Medical Research Specialist

Solutions Engineer

• Lead the design, architecture, and implementation of enterprise Identity and Access Management solutions using SailPoint
• Strengthen access automation capabilities, application security, and GxP/Quality compliance programs
• Translate business, security, and compliance requirements into technical architecture, implementation roadmaps, integrations, and operational processes
• Design and implement enterprise-wide IGA solutions using SailPoint ISC and ServiceNow as a front end
• Define IAM architecture, standards, and best practices
• Create high-level and low-level solution designs, architecture diagrams, and implementation roadmaps
• Evaluate business requirements and translate them into SailPoint technical solutions
• Lead SailPoint implementation projects from design through deployment
• Design and oversee integrations with Active Directory, LDAP, Workday, Fieldglass, Oracle, ServiceNow, Salesforce, O365, and other cloud applications
• Design provisioning and de-provisioning workflows
• Configure access certifications, lifecycle events, role management, policy violations, and segregation of duties
• Provide technical leadership and guidance to IAM engineers, developers, and administrators
• Conduct architecture and design reviews
• Establish governance processes for identity lifecycle management
• Lead client workshops and requirements gathering sessions
• Mentor team members and promote IAM best practices
• Ensure solutions comply with GxP and SOX requirements
• Implement security controls, risk mitigation measures, and audit requirements
• Support internal and external identity-management audits
• Collaborate with business, security, infrastructure, and application teams
• Present architectural recommendations to senior leadership and clients
• Manage technical risks and project dependencies

Senior IT Solution Architect, Access Automation

• Lead commercial enablement readiness for Biogen North America launches within Business Intelligence & Operations
• Translate therapeutic area launch priorities into one BI&O plan with clear owners, milestones, dependencies and resource needs
• Surface unanticipated launch requirements and resolve gaps with functional owners
• Coordinate field readiness, including training and CRM, and Decision Sciences needs such as targeting, data availability and launch dashboards
• Align Marketing Operations and Omnichannel timelines for agency onboarding, promotional review, content delivery and channel activation
• Connect Patient Services and Digital Operations dependencies as needed
• Run readiness reviews, follow through on commitments and resolve handoff gaps
• Escalate risks and resource conflicts with clear recommendations
• Keep BI&O milestones aligned with therapeutic area launch plans
• Confirm capabilities are ready for use and resolve early post-launch issues
• Lead change plans for launches and priority BI&O initiatives
• Identify affected teams, clarify new responsibilities and coordinate communications, training and support
• Track adoption and address barriers with team leads
• Turn launch lessons into practical checklists and playbooks for subsequent launches
• Partner with the BI&O Strategy & Operations team, therapeutic area Strategy & Operations leads, and BI&O functional heads and teams
• Report to the Head of Strategy & Operations

Associate Director, Launch Excellence – Change Management

• Serve as a field-based, customer-facing Medical Science Liaison focused on key medical experts and maximizing medical one-on-one interactions with healthcare professionals
• Conduct more than 70% of activities in the field through face-to-face and virtual interactions
• Act as a scientific expert on Biogen products, disease states, and competitors
• Establish and maintain scientific and strategic relationships with physicians, nurses, allied health professionals, medical societies, and academic centers
• Provide relevant scientific information to key medical experts and organizations
• Facilitate key medical expert participation in educational forums and advisory boards
• Identify key medical experts and collaborate with commercial counterparts on medical engagement
• Develop and implement key medical expert engagement plans and plan visits
• Record healthcare professional interactions and MSL activity in the CRM database
• Provide balanced scientific education and presentations to healthcare professionals
• Source and brief speakers for national and state meetings
• Liaise between investigators and Biogen and gather clinician-driven ideas for data generation activities
• Provide regional medical insights, trends, competitor intelligence, and medical updates to internal teams
• Contribute to medical training for Account Executives and serve as a medical resource for Sales
• Support advisory boards, steering committees, speaker briefings, and clinical trial execution
• Collaborate with medical and commercial teams on strategy and communication of complex scientific information
• Review medical literature, literature alerts, scientific publications, and clinical study findings
• Attend requested national and international conferences and provide summaries to internal stakeholders
• Ensure speaker briefings, contracts, slide reviews, training, and stakeholder interactions comply with SOPs and applicable frameworks

Medical Science Liaison – Alzheimer's Disease

Compliance

• Contribute to the development and implementation of regulatory strategy for specific projects
• Serve as the regulatory representative from Japan on relevant project teams
• Serve as regulatory contact with relevant regulatory authorities
• Manage preparation of submission documents and approval of new drugs, including life cycle management in Japan
• Lead development, alignment, and implementation of Japan regulatory strategy across all development stages
• Provide end-to-end leadership for regulatory submissions in Japan
• Lead meetings and interactions with Japanese Health Authorities
• Translate authority feedback into actions and strategic recommendations
• Identify, assess, and communicate regulatory risks and opportunities
• Develop mitigation and escalation strategies
• Provide recommendations balancing regulatory compliance with risks and benefits of innovative approaches