Biogen

Medical Reviewer

• Lead clinical and scientific data review activities across assigned clinical studies, ensuring data accuracy, consistency, and alignment with protocol expectations and therapeutic objectives.
• Identify insights, trends, and risks through comprehensive data analysis and interpretation, enabling early detection of data quality issues and safety signals.
• Design, test, and refine clinical data review tools—including listings, reports, and visualizations—to support robust data exploration, signal detection, and discrepancy management.
• Collaborate closely with cross‑functional teams, including Clinical Development, Biostatistics, Pharmacovigilance, and Study Operations, to drive data‑driven decision‑making and ensure high-quality trial execution.
• Manage timelines and deliverables with a strong commitment to quality, efficiency, and proactive communication.
• Contribute to risk management by identifying, documenting, and supporting mitigation of study‑level data risks.
• Support strategic initiatives within and beyond the Data Management organization, bringing scientific and operational insight to process innovation and continuous improvement.
• Leverage metrics and analytics to monitor data trends, assess study health, and enhance data review strategies.

Principal Clinical Data Reviewer – Scientist

Director

• Lead the development and ongoing refinement of the integrated plan for one or more assets to maximize value creation and execution.
• Establish and maintain clear asset goals, timelines, and risk management in partnership with project management functions.
• Drive accountability of functional team members and delivery of functional-level plans that integrate with overarching asset strategies.
• Represent the asset at portfolio governance forums and engage with senior stakeholders in the organization.
• Engage proactively with stakeholders and governance to support asset execution and portfolio decision-making.
• Create and maintain conditions for a strong team culture that facilitates effective planning and execution of the asset strategy.
• Actively participate in the department community of practice to share learnings and promote synergies.

Director, Development Asset Lead

Manager

• Serve as the program owner and administrator for Biogen’s Small Business Subcontracting Plan (SBSP), ensuring full compliance with federal requirements.
• Develop, maintain, and submit the annual subcontracting plan, aligning with approved goals and methodologies.
• Prepare and submit mandatory government reports, including spend validation and narrative development.
• Ensure audit readiness by maintaining FAR-required documentation.
• Provide accurate data and narratives for Corporate Responsibility and ESG reporting.
• Maintain high-quality supplier diversity data, including supplier classification and certification tracking.
• Integrate diversity and ESG considerations into category strategies and supplier selection decisions.
• Support sourcing teams to include diverse suppliers in bidding opportunities
• Use spend analytics to identify gaps and sourcing opportunities.
• Ensure seamless execution of guidance provided by CPO and Head of Source to Contract Operations.
• Provide regular performance updates and insights for procurement leadership team.
• Represent the company in supplier diversity networks and conferences.

Associate Manager, Supplier Diversity, Sustainability

Risk

• Translate complex technical and regulatory topics into clear executive briefings, highlighting operational implications, risks, opportunities, and required actions.
• Develop and maintain a forward-looking risk intelligence landscape scanning process for biopharmaceutical manufacturing, process technology, engineering, GMP expectations, and supply chain resilience; convert insights into decision-ready recommendations for senior leaders.
• Lead quantitative and qualitative analyses (trend, scenario, sensitivity, benchmarking) to assess risk and inform decisions for network strategy, capacity planning, and manufacturing investments.
• Build and govern a portfolio of dashboards that integrate data across manufacturing performance, quality, deviations/CAPA, supply, and engineering reliability, ensuring data quality, definitions, and traceability.
• Monitor emerging manufacturing technologies and practices (e.g., digital manufacturing, automation, advanced analytics, continuous manufacturing where applicable) and assess readiness, value, and adoption pathways for Biogen sites and partners.
• Partner with stakeholders to define key questions, prioritize analyses, and align on interpretations and decisions.
• Develop and deliver high-impact materials for PO&T leadership (executive summaries, quarterly landscape reports, and rapid-response briefs).
• Provide analytics and decision support for strategy reviews, business cases, and investment governance (e.g., ROI/NPV/IRR, total cost modeling, and trade-off analyses) for manufacturing and engineering initiatives.
• Establish standards for analytical rigor (methods, assumptions, documentation) and lead peer review of analyses and narratives to ensure accuracy and consistency.
• Drive cross-functional alignment by facilitating structured discussions and workshops that convert insights into plans, owners, and timelines.
• Continuously improve intelligence and analytics processes (data acquisition, automation, taxonomy, and reusable templates) to increase speed, repeatability, and impact.

Director, Risk Intelligence and Analytics

• Partner with cross functional teams to identify critical data and processes (CDPs) and associated study risks
• Contribute significantly to the development and maintenance of the study-specific Risk Assessment Categorization Tool (RACT) or equivalent by providing a clinical data management focused perspective
• Prioritize risks and signals based on patient safety impact, data integrity, severity, likelihood, and detectability
• Conduct proactive, ongoing data reviews using RBQM dashboards and analytics tools
• Ensure timely escalation and follow up on any signals or anomalies
• Review and validate data across EDC, safety, and other clinical systems to ensure consistency and quality
• Oversee data cleaning timelines and ensure adherence to risk mitigation plans
• Document and communicate findings clearly and effectively to study teams
• Trigger and/or support Corrective and Preventive Actions (CAPA)
• Ensure alignment with ICH‑GCP, FDA/EMA regulations, and internal SOPs
• Support audit and inspection readiness related to RBQM and centralized monitoring
• Contribute to and/or lead process enhancements, technology upgrades, and RBQM best practices
• Provide training, guidance, and mentorship on RBQM concepts to study teams.

Senior Principal Risk-Based Quality Management Data Monitor

Communications

• Lead the development of the scientific narrative across planned rheumatology and dermatology indications, emphasizing unmet needs, disease mechanisms, and therapeutic actions.
• Organize and execute scientific symposia at key global medical congresses, aligning with medical objectives.
• Develop scientific content for use by field-based medical personnel, including educational "symposia in a box."
• Create training materials for scientific and medical personnel, supporting onboarding and ongoing education in disease areas and therapeutic assets.
• Chair the scientific narrative cross-functional working group to ensure alignment across departments and the fitness of content for its intended purpose.
• Collaborate with clinical development leads, health economics and outcomes research (HEOR) leads, and publication leads to develop core scientific narratives and content.
• Manage external medical communication vendors, including reviewing and approving statements of work (SOWs) and invoices.
• Navigate complex situations to maintain scientific credibility and accuracy across all content developed for external use.
• Ensure scientific resources are appropriate for various markets/regions, taking into account differing regulatory and compliance considerations.
• Align content development with the core scientific platform, strategic publication plan, and global medical strategy.

Director, Scientific Communications – Lupus

Analyst

• Perform batch release testing in QC Chemistry and Microbiology areas
• Conduct chromatographic analyses including HPLC and Gas Chromatography
• Execute microbiological routine tests and microbial limits testing
• Maintain robust and compliant cGMP documentation practices
• Support equipment and instrument calibration program
• Participate in strategic projects and external team initiatives
• Collaborate in investigations and implement corrective actions
• Manage deviations, CAPA, Change Control, and other quality tools
• Support method validation and author protocols and reports
• Assist and contribute to training programs for employees
• Represent QC in audits and inspections with Health Authorities

Quality Control Analyst

Recruitment

• Influence and shape workforce planning with business and HR leaders by providing market intelligence, talent insights, and hiring feasibility assessments.
• Utilize analytics to inform TA strategy and drive operational efficiency.
• Oversee TA staff and service delivery for R&D & WCH, including management of FTEs, contractors, and outsourced solution providers.
• Coach and develop a high-performing Talent Acquisition team, enhancing stakeholder management, recruitment processes, and data-driven strategies.
• Manage a complex network of cross-functional stakeholders to ensure seamless, compliant, and efficient hiring processes.
• Optimize relationships with external partners, ensuring quality and cost-effectiveness.
• Implement localized branding and attraction strategies to elevate Biogen's presence among target talent populations.
• Champion a best-in-class candidate experience across all touchpoints, aligning with Biogen’s values.
• Collaborate with TA Centers Of Excellence to deliver comprehensive TA services to R&D & WCH.
• Drive adoption and optimization of TA technologies and tools to enhance recruiter effectiveness.
• Act as a key leader within Global Talent Acquisition, driving cross-functional projects to strengthen TA’s functional capacity.

Talent Acquisition Leader – R&D

• Build trusted relationships with patients and healthcare providers through proactive communication and timely execution of deliverables.
• Leverage a thorough understanding of program services to align support with the unique needs of each patient.
• Deliver personalized case management, including inbound and outbound communication with patients and HCPs regarding non-clinical access challenges.
• Provide personalized reimbursement support, including benefit investigations, prior authorization information, and financial assistance program determination.
• Conduct necessary benefits, coverage, and payer research to ensure compliance with appeal policies and timelines.
• Adhere to all standard operating procedures and departmental guidelines.
• Travel up to 20% to support program operations.
• Meet and exceed performance metrics and quality standards to achieve business objectives.
• Perform other duties as assigned.

Senior Case Manager – Specialty

Procurement

• Oversee clinical program sourcing and contracting processes.
• Collaborate with cross-functional teams to ensure project success.
• Analyze and manage vendor contracts and relationships.
• Monitor project timelines and budget adherence.

Senior Analyst II, Clinical Program Sourcing – Contracting Management

• Partner with business stakeholders across US Commercial functions including Field Operations, Marketing Operations, Decision Sciences, and Patient Services to understand strategic objectives, pain points, and decision needs.
• Lead requirements discovery, documentation, and validation, including functional, non‑functional, and data requirements.
• Ensure requirements are backlog-ready for sprint-level execution.
• Translate data architecture and integration outcomes into clear, business‑friendly language for non‑technical audiences.
• Collaborate with technical teams to shape data models, curated datasets, and semantic layers aligned to business needs.
• Lead the integrations design across cross functional systems to understand data pipeline dependencies and data flows.
• Participate in design discussions and trade‑off decisions.
• Lead the design, implementation, and governance of data integrations across Snowflake, Databricks, Veeva CRM, SFMC, CDP, and other commercial platforms supporting advanced analytics use cases such as decision engine, adoption journey, segmentation, or ML‑enabled insights.
• Lead integration design documentation, mapping data pipeline dependencies and data flows to inform architecture decisions.
• Partner with data engineering, Data Management (DMA IT), Enterprise Applications Solutions (EAS), AI Capability Technology (AICT) and Global Commercial and Medical (GCM) IT teams to define integration patterns (batch, real-time, API-based, event-driven) and ensure data consistency, timeliness, and compliance.
• Participate in and enforce data governance standards, including data access governance, data lineage, consent management, and regulatory compliance (e.g., HIPAA, privacy requirements) for all integration touchpoints—especially those involving patient-level data.
• Proactively identify integration risks, gaps, and dependencies; drive resolution through cross-functional collaboration and escalation when needed.
• Operate within Biogen's SAFe Agile Release Train (ART), contributing to PI Planning, backlog grooming, sprint execution, and release readiness activities.
• Coordinate with vendor and contract delivery partners (e.g., offshore data engineering teams) to manage integration deliverables, acceptance criteria, and testing milestones.

IT Data Integration Lead

• Partner with cross-functional teams including clinical operations, biostatistics, data management, regulatory, and safety to advance early-phase development programs.
• Contribute to clinical trial protocol design, development and execution for early phase neuroimmunology studies.
• Provide medical monitoring, clinical execution, and oversight of clinical studies to ensure patient safety.
• Serve as a contact for CRO and investigators to provide responses for protocol related questions.
• Provide scientific therapeutic expertise to internal and external stakeholders.
• Support data interpretation and clinical reporting for early phase clinical studies.
• Support preparation for health authority interaction and contribute to responses for regulatory questions related to clinical development activities.
• Contribute scientific contents for clinical protocols and other clinical development documents.
• Support risk mitigation strategies and provide clinical input for safety management plans.
• Assist in providing scientific content for clinical study documents such as protocols, amendments, investigator brochure, clinical study reports, and briefing materials.
• Champion patient-centered development approaches by incorporating disease burden, feasibility and patient experience considerations into study design.
• Monitor the external landscape in neuroimmunology and autoimmune disease, including competitive intelligence, evolving standards of care, and relevant scientific advances.

Associate Director, Clinical Development – Immunology

Financial Planning and Analysis

• Lead Biogen’s medium and long-range planning efforts.
• Build and maintain Biogen’s corporate finance model to project and analyze impacts of product performance, R&D portfolio decisions, capital allocation strategy, and business development deals.
• Perform sum-of-the-parts valuation analysis, quantifying projected shareholder value creation under various scenarios.
• Communicate strategic opportunities and critical issues related to the company’s financial trajectory to senior management.
• Partner with Corporate Strategy leaders to align financial trajectory with strategic direction and future goals.
• Determine optimal return of excess capital to shareholders.
• Assess historical ROI to inform future investment decisions.
• Support Corporate Strategy team in prioritizing portfolio investments.
• Drive forecasting process improvement and automation.

Manager – Corporate Finance

Account Manager

• Supporting the brand strategies for in-line products and launch planning for pipeline products by executing Trade & Distribution strategies that ensure product supply to all dispensing locations servicing customers and patients.
• Negotiation and management of Specialty Pharmacy distribution agreements including tracking of performance metrics and management of existing agreements to ensure mutual compliance between SPs and Biogen. Responsible for creating the agenda, content and business objectives for QBRs.
• Will lead the coordination with PS colleagues and discuss/identify opportunities to streamline gross to net.
• Manage the onboarding process for Alternate Pharmacy Network that includes both independent and IDN specialty pharmacies who have met criteria and been approved by the Director, Trade & Distribution and Distribution Committee.
• Identify opportunities within SP accounts and implement strategies and tactics with the goal of growing Biogen business.
• Communicate strategic direction and related concepts across internal and external customers. Utilize availability of SP data in order to communicate with all stakeholders on trends impacting Biogen’s business.
• This position will work closely with T&D’s Sr. Manager, Pharmacy Operations and Data and Insights team.
• Participate in Specialty Distribution channel association meetings to foster relationships with SP partners and to increase knowledge of channel changes and opportunities. (i.e., CBI conferences, PCMA, Asembia Summit)

Senior National Account Manager, Specialty Channel

Account Executive

• Develop and lead Anthem account strategy to secure and optimize formulary access, coverage, and reimbursement across Commercial, and Medicare, and Medicaid segments.
• Own account enterprise relationships across multiple levels within the Anthem organization, ensuring ongoing engagements with key decision makers influencing coverage, utilization management, and contracting decisions.
• Execute contracting strategies, including rebates, administrative fee agreements, value-based contracts, and pull-through initiatives, in alignment with pricing and compliance requirements.
• Collaborate cross-functionally with MA&R, Franchise Leadership, Trade & Distribution, Regional Account, Legal, Medical and Value Access & Optimization teams to ensure coordinated execution of payer strategies.
• Support product launches and lifecycle management, driving early access readiness, formulary positioning, and post-launch optimization across all payer channels.
• Analyze payer performance metrics, including formulary status, utilization trends, contract compliance, and financial outcomes, to inform strategic decision-making.
• Proactive Communication on across Biogen NA on key aspects related to the nation payers, including formulary updates, coverage policies, account trends and business opportunities
• Ensure compliance with government pricing, Medicaid Best Price, Anti-Kickback Statute, and internal policy requirements across all contracting and payer engagements.
• Translate complex payer dynamics—including utilization management, benefit design, and health-economic evidence—into actionable strategies for internal stakeholders.
• Represent the organization externally at national payer meetings, negotiations, and industry forums, reinforcing the company’s value proposition and partnership approach.