Lead the design, architecture, and implementation of enterprise Identity and Access Management (IAM) solutions using the SailPoint platform. Collaborate with cross-functional teams to ensure access lifecycle, provisioning, and compliance requirements are met effectively.
The Family Access Manager acts as a patient-facing expert, coordinating with cross-functional teams to resolve logistical and non-clinical barriers to therapy access. They provide education and support to patients, families, and healthcare providers while managing regional patient advocacy activities.
The Account Manager is responsible for developing and executing sales plans while building relationships with healthcare providers to drive PPD screening and treatment initiatives. They must effectively communicate complex clinical data and market access policies to key stakeholders within their assigned territory.
The Associate Director will execute marketing strategies and field-based tactics to support the Rheumatology franchise and immunology portfolio. This role involves engaging with key medical experts, managing advisory boards, and providing competitive insights to inform brand activities.
The Associate Director will execute field-based marketing strategies and tactics to support the Rheumatology franchise and immunology portfolio. They are responsible for generating insights from key medical experts, managing advisory boards, and coordinating promotional activities within their assigned region.
The Thought Leader Liaison will execute field-based strategies to support educational goals and product therapy use within the dermatology and immunology franchise. This role involves managing key medical expert relationships, leading advisory boards, and providing competitive insights to internal brand teams.
The Thought Leader Liaison will execute field-based strategies to support educational goals and product therapy use within the Dermatology and immunology portfolio. This role involves managing key medical expert relationships, leading advisory boards, and providing competitive insights to inform brand activities.
The Thought Leader Liaison will execute field-based strategies to support educational goals and product therapy use within the dermatology and immunology franchise. This role involves managing key medical expert relationships, leading advisory boards, and providing competitive insights to cross-functional brand teams.
The Senior Clinical Trial Transparency Specialist leads clinical trial transparency activities, ensuring accurate and timely disclosure of trial registration and results. They coordinate with study teams and vendors to oversee disclosure planning, quality review, and process improvements.
The Key Customer Manager is responsible for developing and executing engagement plans for key medical experts and accounts to drive the success of the Biogen MS portfolio. They facilitate a strategic engagement approach by collaborating with cross-functional partners and local sales teams to improve patient access and quality of care.
The Senior Medical Science Liaison acts as a scientific expert to establish strategic relationships with healthcare professionals and facilitate scientific knowledge exchange. They are responsible for executing engagement plans, gathering business insights, and collaborating with internal teams to support medical strategy and clinical trial execution.
The Director of Medical Writing oversees complex clinical and regulatory documentation for the West Coast Hub, ensuring alignment with global standards and therapeutic area strategies. They provide leadership and mentorship to medical writing staff while collaborating with cross-functional teams to support regulatory submissions and departmental growth.
The Account Manager is responsible for developing and executing sales plans while building relationships with healthcare providers to drive treatment pathways for Post-Partum Depression. They must effectively communicate complex clinical data and market access policies to key stakeholders in their assigned territory.
The role is responsible for optimizing internal operations, communications, and strategic initiatives within the Statistical Sciences & Evidence Generation (SSEG) department. It involves driving operational excellence, managing budgets, and overseeing strategic projects to ensure the organization remains future-ready.
The lead will develop and execute global regulatory strategies for medical devices and combination products while representing the CMC function on cross-functional teams. They are responsible for authoring regulatory submissions, managing health authority interactions, and ensuring compliance with global standards.
The Medical Science Liaison engages with Key Medical Experts and healthcare professionals to communicate the clinical and scientific narrative of Biogen's therapies. They are responsible for capturing medical insights and building strategic, long-term relationships to improve patient outcomes.
The Associate Director will lead the end-to-end integration of digital health and emerging technology assets into clinical trials. They will coordinate cross-functional efforts between data science teams, external vendors, and clinical operational staff to ensure program delivery and regulatory compliance.
The Care Network Manager will collaborate with healthcare professionals to identify patients with rare diseases and facilitate referrals to specialized centers. They are responsible for developing omnichannel engagement plans and optimizing patient pathways to enhance brand perception and market presence.
The Key Account Manager is responsible for driving patient identification and market development for rare diseases by executing territory strategies and building relationships with healthcare providers. They coordinate with internal teams to ensure product success and facilitate healthcare decisions while adhering to strict ethical and compliance standards.
The Clinical Country Site Lead provides local operational and scientific expertise to support global clinical development strategies and ensures successful trial delivery. They act as a key liaison between investigators, research sites, and global study teams while overseeing CRO activities and maintaining regulatory compliance.
The Associate Clinical Country and Site Lead supports global clinical development strategy by providing local operational and scientific expertise. They serve as the primary point of contact for clinical sites, ensuring quality execution, patient safety, and effective investigator engagement.
Lead the strategy, direction, and execution of the national Nurse Educator program to support patient services and brand objectives. Manage vendor partnerships and a geographically dispersed team to ensure consistent, high-quality patient experiences throughout their therapy journey.
The Key Customer Manager is responsible for developing and executing engagement plans for key medical experts and accounts to drive the success of the MS portfolio. They facilitate a strategic engagement approach while collaborating with cross-functional partners to improve patient access and quality of care.
The Medical Science Liaison will serve as a scientific expert to engage with Key Medical Experts and healthcare professionals to improve clinical decision-making. They will also manage strategic relationships and report medical insights to inform clinical strategies.
The MSL serves as a scientific expert engaging with Key Medical Experts and healthcare professionals to improve clinical decisions and patient outcomes. Responsibilities include building strategic long-term relationships and reporting medical insights via Veeva to inform clinical strategies.
Act as a scientific expert to engage with Key Medical Experts and healthcare professionals to improve clinical decisions regarding Biogen's therapies. Build strategic long-term relationships and capture medical insights using Veeva to inform clinical strategies.
The Associate Director serves as a strategic partner to the Head of Sales, managing the operational cadence and business governance of the Neuropsychiatry sales organization. This role focuses on translating leadership priorities into measurable execution, driving organizational effectiveness, and coordinating cross-functional initiatives.
Lead the delivery of global access management services, establishing policies, standards, and automation strategies to improve service efficiency. Manage the full lifecycle of digital identities and ensure compliance with regulatory requirements like SOX and GxP.
Contribute to the design and execution of early-phase clinical trials for immunology programs focusing on autoantibody-driven diseases. Partner with cross-functional teams to develop protocols, provide medical monitoring, and support regulatory interactions.
Drive strategic scientific engagement and provide medical support to key experts and patient advocacy groups to bolster pipeline development in Germany. Lead expert discussions, deliver complex scientific presentations, and collect medical insights to inform local strategy.
The Associate Director will provide pharmacometrics expertise for high-priority clinical development programs, contributing to strategy and supporting quantitative decision-making through advanced modeling and simulation. This role involves executing advanced analyses like PK/PD modeling and communicating results to program teams to support data-driven decisions.
The Associate Scientific Director will provide strategic leadership in developing and executing clinical pharmacology plans for drug candidates, integrating knowledge to optimize dosage regimens and study designs throughout the drug development lifecycle. This role involves leading the execution of clinical pharmacology studies, conducting hands-on quantitative analysis, and serving as the subject matter expert in interactions with Health Authorities.
The Clinical Country Site Lead (CCSL) provides local operational and scientific expertise to support global clinical development strategy and ensures the delivery of local clinical trials. This role acts as a primary contact for CRO staff and global teams, focusing on quality, patient safety, and oversight of monitoring activities.
