Biogen

Account Manager

• Drive patient identification and market development for FA by building and executing against a territory strategy and HCP specific plans. Continuously assesses sales opportunities within markets and accounts to maintain and grow their business.
• Builds and maintains relationships with physicians by maximizing their time through pre-call planning, leveraging insights to tailor a call plan, and conducts post call analysis to continually refine and enhance their approach.
• Proactively builds effective working relationships with internal/external stakeholders; can drive agreement/decisions from multiple stakeholders; can read people’s emotions and flex communication style.
• Collaborate with stakeholders across commercial, compliance, and patient care centers to ensure access at site of care and that logistics are in place to administer.
• Collaborate with key offices and physicians to build individual plans on how to approach their customers, achieve sales goals, and maintain relationships in order to maximize sales results.
• Execute programs, in-services, and lunch-and-learns for their territory.
• Determines suitable travel schedule and call plan on a daily/weekly basis to ensure adequate coverage for all key customers.

Neurology Account Manager – Friedreich's Ataxia

Data Scientist

• Support the design, specification, and development of eCRFs, ensuring adherence to Biogen standards throughout.
• Coordinate the development and testing of clinical data management systems edit checks and listings/reports/tools for data review and discrepancy management activities.
• Support the development of Data Management Plan documents that will ensure delivery of accurate, timely, consistent, and high-quality clinical data.
• Works with Third Party /External data Vendors to complete the set-up of data import and reconciliation processes.
• Perform comprehensive review of all data generated from the clinical study including Third Party/External data, SAE data and local lab data, as applicable.
• Oversees quality control procedures.
• With guidance from Principal Clinical Data Lead or Manager, effectively manage project timelines and quality.
• Provide reports, status updates, feedback and advice to key study stakeholders on the progress of data cleaning and risk identification/mitigation activities.
• Ensures activities that are performed are in with line Biogen’s processes, GCP, Regulatiory Guidelines and Best Practices.
• Provide back up support for Principal Clinical Data Lead as required.

Senior Clinical Data Manager

Procurement

• Be a Vendor Ambassador and/or lead oversight of key clinical trial vendor services at the category level to drive performance, including issue management and inspection readiness, collaborating with functional SMEs.
• Lead Biogen cross functional teams in strong, compliant governance activities, building transparent communication channels within vendor relationships.
• Drive development and execution of vendor oversight plans across functional areas.
• Establish key performance indicators for vendor services, managing risks and promoting continuous improvement.
• Align vendor engagements with corporate policies, working with Global Sourcing, R&D IT, and Compliance teams.
• Lead/drive projects and initiatives that relate to vendor qualification, selection, performance oversight, and governance activities.
• Lead or contribute to development of department systems, processes, and templates.
• Line manages personnel directly or in-directly to support a people management matrix, as per business needs.

Associate Director, SRPO Vendor Management

Payroll

• Process regular and off-cycle US and Canada payroll, including collecting payroll inputs and calculating payroll to ensure timely payment to employees
• Ensure all payroll transactions comply with internal policies and procedures, as well as government regulations, including timely tax payments and document filing
• Provide support to team members when needed by acting as a backup and participating in knowledge sharing
• Keep process documentation up to date and suggest improvements to promote efficiency and systems optimization
• Deliver exceptional support to employees and stakeholders, resolving tickets and requests promptly and ensuring regular communication
• Collaborate with other departments to support payroll-related projects and initiatives

Senior Payroll Specialist

Account Executive

• Drive patient identification and market development for SMA & ALS by building and executing against a territory strategy and account specific plans.
• Continuously assesses sales opportunities within markets and accounts to maintain and grow their business.
• Able to effectively prioritize time, activities, and resources to optimize accounts with the most sales potential.
• Can educate and promote Biogen services.
• Builds and maintains relationships with physicians by maximizing their time through pre-call planning, leveraging insights to tailor a call plan, and conducts post call analysis to continually refine and enhance their approach.
• Proactively builds effective working relationships with internal/external stakeholders; can drive agreement/decisions from multiple stakeholders; can read people’s emotions and flex communication style.
• Can adjust their approach based on different stakeholder needs, concerns, or audience member to drive alignment and meet their work goals.
• Collaborate with stakeholders across commercial, compliance, and patient care centers to ensure access at site of care and that logistics are in place to administer.
• Collaborate with key accounts and physicians to build individual account plans on how to approach their customers, achieve sales goals, and maintain relationships in order to maximize sales results.
• Collaborate with key accounts and physicians to drive patient identification through market development and physician education; post launch be able to develop a territory strategy to retain customers.
• Executes programs, in-services, and lunch-and-learns for their territory.
• Determines suitable travel schedule and call plan on a daily/weekly basis to ensure adequate coverage for all key accounts.

Rare Disease Account Executive

Security Engineer

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Managed Service Lead, Cybersecurity

Manager

• Develops and oversees implementation of the study-level operational strategy for the successful delivery of clinical study(ies)
• Chairs the SMT to drive the development of scientifically robust, operationally feasible, and clear protocol concepts/protocols
• Collaborates strategically with the core SMT (study MD, biostatistics, etc.) and other key program team members to provide direction on phase, disease, or therapeutic area to support study design in alignment with the Integrated Development Plan and Global Program Strategy, enabling protocol concept development and driving forward studies through governance approval
• Leverages operational expertise and scientific assessment to evaluate study feasibility and support protocol development
• Aligns team perspectives to develop a cross-functional operational strategy, leveraging expertise, current therapeutic knowledge, and relevant supporting data
• Effectively leads the study via oversight of the CRO, managing performance, quality, and timelines, including defining and delivering against a baseline plan
• Ensures ongoing data review to identify and mitigate patient safety, study design, data integrity or study conduct issues
• Exhibit financial management & analysis skills to ensure budgets hold up to appropriate scrutiny and align with study endpoint needs
• Oversees the delivery of studies by CROs, ensuring quality execution in line with time and budget forecasts
• Chairs the Study Management Team (SMT) in partnership with the CRO SMT Lead; ensures the CRO creates appropriate risk mitigation plans and is effective in proactively identifying and resolving issues
• Establishes and drives effective and efficient team operations by setting culture of SMT, ensuring thorough team communication, effective goal setting/management and oversight of strategy implementation
• Ensures all operational aspects of the study(ies) conduct support patient safety, endpoint integrity and data validity
• Demonstrates a robust understanding of the study design, rationale, endpoints, and patient population
• Provides oversight via ongoing review of performance and partnership metrics to ensure key milestones and deliverables are achieved
• Ensures that all project plans (e.g. Monitoring Plan, Quality Plan, etc.) are in place for effective implementation of studies
• Leads SMT to develop robust Baseline plans, and ensures team is thoroughly prepared for all key governance forums including but not limited to, Baseline, Study Delivery forum, etc.
• Proactively & robustly manages inflection points to ensure any necessary course correction is proactively addressed
• Collaborates with CFP and procurement functions to ensure FMV is achieved and budget oversight responsibilities are met.
• Maintains data accuracy, completeness and quality within study-related systems (e.g. Clarity, Impact, etc.)
• Strives for effective, consistent, efficient, and compliant processes
• Champions best practices and seeks opportunities for innovation and efficiency within CTDU and GCO
• Seeks synergies and commonalities with other studies, programs, and development units to enhance excellence in study planning and execution
• Seeks ways to improve and streamline processes to support the GCO CRO outsourcing models; provides feedback via appropriate channels for opportunities to improve processes or establish best practices
• Embodies a culture of continuous improvement by seeking consistency and efficiency in processes and fully supporting the CRO partnership model
• Advocates for the CTDU group and actively promotes interaction with other Biogen groups
• Promotes a rich and diverse knowledge base within CTDU, contributing SME expertise where applicable

Senior Manager, Clinical Trial Lead

Compliance

• Oversee the management and coordination of regulatory CMC activities across assigned projects and products.
• Lead cross-functional teams responsible for global RegCMC submissions (IND/IMPD/CTAs, NDAs/MAAs) and responses to Health Authority questions.
• Define and implement global RegCMC regulatory strategy to support development and commercial objectives.
• Communicate RegCMC strategies, risks, and plans effectively to leadership and project teams.
• Ensure regulatory strategies align with business goals and meet Health Authority requirements.
• Monitor and influence global RegCMC environment changes; contribute to internal process and policy improvements.
• Mentor and coach team members, supporting skill development within the RegCMC organization.
• Lead regulatory assessments, ensuring compliance with evolving global CMC regulations, and maintaining strong relationships with global health authorities.

Associate Director, Regulatory CMC Small Molecule Lead

• Drive patient identification and market development for FA by building and executing against a territory strategy and HCP specific plans.
• Continuously assesses sales opportunities within markets and accounts to maintain and grow their business.
• Able to effectively prioritize time, activities, and resources to optimize patient identification.
• Can educate and promote Biogen services.
• Builds and maintains relationships with physicians by maximizing their time through pre-call planning, leveraging insights to tailor a call plan, and conducts post call analysis to continually refine and enhance their approach.
• Proactively builds effective working relationships with internal/external stakeholders; can drive agreement/decisions from multiple stakeholders; can read people’s emotions and flex communication style.
• Can adjust their approach based on different stakeholder needs, concerns, or audience member to drive alignment and meet their work goals.
• Collaborate with stakeholders across commercial, compliance, and patient care centers to ensure access at site of care and that logistics are in place to administer.
• Collaborate with key offices and physicians to build individual plans on how to approach their customers, achieve sales goals, and maintain relationships in order to maximize sales results.
• Collaborate with key offices and physicians to drive patient identification through market development and physician education; post launch be able to develop a territory strategy to retain customers.
• Executes programs, in-services, and lunch-and-learns for their territory.
• Determines suitable travel schedule and call plan on a daily/weekly basis to ensure adequate coverage for all key customers.

Community Manager

• Support various aspects of our teams vital activities including:
• Conduct research on rural health disparities relevant to priority disease areas, including: Diagnostic and care deserts; Coverage and access barriers; Barriers to clinical research participation and real-world care
• Synthesize insights to inform medical affairs disease strategy, evidence gaps, and scientific priorities
• Support development of a rural health equity engagement framework aligned with Biogen’s medical affairs and health equity objectives
• Support medical affairs led evidence development by identifying gaps related to rural and underserved populations
• Translate qualitative community insights into scientifically relevant considerations for medical affairs teams
• Assist in planning and participating in community engagement activities to gather medical and scientific insights
• Document and synthesize feedback to inform medical affairs strategy and evidence planning
• Support development of scientifically accurate, culturally appropriate educational materials for rural audiences
• Contribute to disease awareness and clinical research education efforts consistent with medical affairs standards
• Collaborate with internal medical affairs partners to ensure rural health equity insights are reflected in broader scientific initiatives
• Complete at least one Health Equity Disease Literature and Insights Overviews aligned with medical affairs standards

Intern, Health Equity & Clinical Innovation – Rural Community Engagement

Artificial Intelligence

• Collaborate with the AI team on innovative projects
• Participate in the development of AI models
• Support the implementation of AI solutions in Biogen's processes
• Engage with cross-functional teams to drive initiatives

Co-op, Artificial Intelligence Innovation

• Support various aspects of our team's vital activities including:
• Map how health equity considerations are currently incorporated—or absent—across key medical affairs activities, including:
• Disease strategy development and medical planning
• Evidence generation and Phase IV / real-world evidence planning
• Scientific education, disease materials, and content development
• External scientific engagement and stakeholder planning
• Review existing medical affairs templates, guidance documents, and workflows to assess consistency and completeness of equity integration
• Identify integration opportunities to embed health equity into existing standard medical affairs processes (e.g., added prompts, sections, or decision considerations)
• Propose updates to:
• Medical strategy and planning templates
• Evidence generation frameworks
• Education (internal and external) and engagement planning tools
• Ensure all recommendations are practical, scalable, and aligned with medical affairs governance and compliance expectations
• Develop 1–2 internal medical affairs education modules/presentations focused on understanding health equity and applying health equity principles in day-to-day medical affairs work
• Create a health equity “quick reference” for disease teams, translating academic and public health concepts into clear, medical affairs relevant guidance
• Support development of practical tools that help medical affairs teams:
• Ask the right equity-focused questions during planning
• Identify evidence and education gaps
• Apply equity considerations consistently across disease areas
• Translate findings into clear, medical affairs ready insights and visual summaries
• Support development of briefing materials and presentations for medical affairs and Health Equity leadership
• Contribute to internal alignment by framing equity as an enabler of scientific rigor, relevance, and impact
• Complete at least one Health Equity Disease Literature and Insights Overviews aligned with medical affairs standards, including:
• Epidemiology and disease burden
• Demographic and geographic variation
• Severity, comorbidities, and outcomes
• Economic burden and access challenges, Diagnostic delay
• Racial/ethnic, age, and gender differences
• Quality of life and caregiver impact
• Published patient reported outcomes, patient experience and real-world data
• Present findings including opportunities for Biogen medical teams to medical affairs and Health Equity team members at the conclusion of the internship
• Support medical affairs aligned community outreach initiatives
• Support ad hoc medical affairs or Health Equity projects as needed
• Contribute to synthesis decks, briefing documents, and insight summaries for internal stakeholders

Intern, Health Equity & Community-Centered Innovation

Director

• Provide clinical pharmacology expertise to program and study teams throughout a molecule’s lifecycle (discovery through development) Provide functional representation on development program s and study teams and identify opportunities where modeling and simulation can ad vance the understanding of pharmacological activity, efficacy and safety Develop & implement the clinical pharmacology development plan, considering all aspects (strategic, scientific, translational, and clinical) Define key milestones and decisions within the clinical pharmacology development plan and identify risks and mitigation strategies Lead execution of clinical pharmacology studies & analyses; interpret results and recommend action based on results Conduct hands - o n quantitative ana lysis and present the findings to multidisciplinary project teams Serve as lead author and key contributor to clinical pharmacology sections of documents Serve as the subject matter expert in interactions with Health Authorities Seek input from and ensure alignment with cross-functional partners, consultants, experts, and vendors as needed Work with program and/or study teams to achieve program goals and provide deliverables in approved timeframes Maintain cutting edge knowledge of best regulatory practices, quantitative/clinical pharmacology methodology , and drug development precedent ​

Associate Scientific Director, Clinical Pharmacology

• Provide regulatory strategic input, risk assessment, and mitigation strategies to various global and U.S. internal teams on branded and unbranded concepts, promotional materials, disease awareness communications, medical communications and sales training/education materials
• Provide creative and solution-oriented feedback to meet business goals and further business objectives
• Serve as the primary point of contact with the Office of Prescription Drug Promotion (OPDP) for designated product(s)
• Ensure promotional materials are consistent with FDA-approved labeling, compliant with applicable FDA regulations, and completed in accordance with 2253 submission requirements
• Develop and maintain strong working relationships with internal colleagues including, but not limited to: Commercial, Medical, Legal, Compliance, Regulatory Strategy and Labeling, and Medical/Marketing Operations
• Work with management and Reg AP team members to ensure communications and feedback are generally consistent across franchises
• Assist Regulatory Ad Promo department in monitoring evolving regulatory landscape and communicating updates to internal stakeholders

Associate Director, Regulatory Affairs – Advertising and Promotion

• Sell Neurology products to stakeholders in the Multiple Sclerosis community
• Develop and execute on sales plans for assigned territory
• Convey complex clinical and reimbursement information to customers and key stakeholders
• Utilize interpersonal skills to address customer educational needs
• Work closely with cross functional peers for customer education on Biogen support services

Neurology Account Manager – Friedreich's Ataxia

Senior Clinical Data Manager

Associate Director, SRPO Vendor Management

Senior Payroll Specialist

Rare Disease Account Executive

Managed Service Lead, Cybersecurity

Senior Manager, Clinical Trial Lead

Associate Director, Regulatory CMC Small Molecule Lead

Neurology Account Manager – Friedreich's Ataxia

Intern, Health Equity & Clinical Innovation – Rural Community Engagement

Co-op, Artificial Intelligence Innovation

Intern, Health Equity & Community-Centered Innovation

Associate Scientific Director, Clinical Pharmacology

Associate Director, Regulatory Affairs – Advertising and Promotion

Senior Territory Business Manager – Multiple Sclerosis