The Associate Director will independently represent Clinical Pharmacology to support clinical stage project teams and guide development decisions. They are responsible for leading the analysis, interpretation, and reporting of clinical pharmacology data, including contributions to regulatory submissions and clinical protocols.
The Director will lead the US labeling function and develop global labeling strategies, including the maintenance of Company Core Data Sheets and Target Label Profiles. They will also provide strategic guidance on regulatory requirements and represent the Global Labeling team in cross-functional governance forums.
The Key Account Manager is responsible for developing and implementing strategic account plans to drive commercial objectives and patient diagnosis rates within their assigned territory. They collaborate cross-functionally with medical, marketing, and market access teams to ensure optimal patient care and product access while maintaining high ethical standards.
The Area Sales Manager leads and develops a team of Key Account Managers to drive commercial strategy and patient outcomes in Central Italy. They are responsible for translating brand strategy into effective field execution while ensuring full compliance with industry laws and company policies.
The Field Reimbursement Manager serves as a subject matter expert, educating healthcare providers on reimbursement pathways and coverage requirements to ensure patient access. They coordinate with the Hub and cross-functional teams to address access barriers and manage individual patient cases effectively.
The Senior Manager, Medical Writing will lead the development of clinical documents while ensuring compliance with regulatory standards and Good Clinical Practices. They will also oversee contract writers and collaborate with cross-functional teams to manage project timelines and deliverables.
The Senior Manager is responsible for the strategic planning, development, and implementation of training programs for Market Access and Strategic Accounts teams. They will collaborate cross-functionally to ensure compliant delivery of training materials and use performance data to identify capability gaps.
The Site and Monitoring Health Lead implements oversight strategies to ensure clinical trial quality and CRO monitoring effectiveness in alignment with GCP standards. They manage site risks, conduct oversight activities, and collaborate with cross-functional teams to resolve issues impacting clinical site delivery.
The HS MOSL serves as a field-based scientific expert engaging with health system leaders to provide evidence-based information and support formulary and access decisions. They are responsible for developing account-specific strategic plans, identifying research collaboration opportunities, and communicating the clinical and economic value of the company's portfolio.
The Associate Director of Biostatistics leads statistical activities for clinical trials, including protocol design, statistical analysis planning, and data interpretation. They collaborate with cross-functional teams and regulatory bodies to support the clinical development of drug candidates.
The Senior Manager will lead clinical data management activities, including database builds, data cleaning, and CRO oversight for global studies. They will also provide strategic guidance to direct reports and ensure compliance with regulatory standards and inspection readiness.
The Case Manager assesses patient needs to develop action plans for treatment initiation and maintenance while coordinating with internal and external stakeholders. They manage the reimbursement process, including insurance approvals, billing, and patient assistance programs to ensure seamless access to therapy.
The HS MOSL serves as a field-based scientific expert engaging with health system leaders to provide evidence-based information and support formulary and clinical pathway decisions. They are responsible for developing account-specific strategic plans, gathering scientific insights, and identifying research collaboration opportunities.
The Associate Case Manager supports patient access and therapy management by verifying insurance coverage and coordinating with payers and providers. They are responsible for maintaining accurate patient data, managing incoming referrals, and navigating the CRM platform to ensure efficient service delivery.
The Associate Director of Field Operations drives the effectiveness and operational excellence of customer-facing teams across Commercial and Medical Affairs. This role translates business strategy into actionable execution frameworks, including performance metrics, targeting, and operational cadence.
The Senior Manager develops and implements capability-building strategies to drive field performance and business outcomes within the TTR franchise. They collaborate with cross-functional teams to design high-impact learning experiences and manage onboarding and continuous development programs.
The Principal Medical Writer leads the development of high-quality clinical documents and oversees the work of contract writers on multi-disciplinary teams. They ensure compliance with regulatory standards while collaborating with internal and external stakeholders to facilitate efficient document review and finalization.
The MSL will build and sustain scientific partnerships with key opinion leaders and healthcare professionals to elevate disease understanding of TTR amyloidosis. They are responsible for identifying unmet medical needs, delivering balanced scientific information, and gathering actionable insights to support strategic medical priorities.
The Director leads the development of financial and operational capabilities for pricing and contracting, including deal modeling and GTN/ASP forecasting. They partner with cross-functional teams to provide actionable insights and implement data-driven strategies to improve decision quality.
The Business Account Executive is responsible for driving physician and patient identification, disease awareness, and brand growth within their assigned territory. They will manage account strategies, collaborate with internal stakeholders, and execute educational programs to achieve sales objectives.
The Senior Manager will develop and implement capability-building strategies to drive field performance and business outcomes within the TTR franchise. They will collaborate with cross-functional teams to design high-impact learning experiences and manage onboarding and continuous learning programs.
The Business Account Executive is responsible for driving patient identification, disease awareness, and brand growth within the South Alabama territory. They will manage account strategies, collaborate with internal stakeholders, and build relationships with healthcare professionals to achieve sales objectives.
The Business Account Executive is responsible for driving disease awareness, patient identification, and brand growth within the Pacific Northwest territory. They will manage account strategies, collaborate with internal stakeholders, and execute educational programs to achieve territory sales objectives.
The Principal Clinical Data Manager leads data management activities for clinical studies, including database builds, vendor oversight, and cross-functional collaboration. They are responsible for ensuring data integrity, managing study timelines, and driving inspection readiness for clinical data systems.
The Director leads the development of financial and operational capabilities for pricing and contracting decision-making across the organization. They are responsible for deal modeling, GTN/ASP forecasting, and establishing data standards to support market access and commercial strategies.
The Associate Director will optimize patient access to Alnylam products by addressing reimbursement challenges and educating sites of care. They will manage access issues, build strategic relationships with external stakeholders, and lead tactical plans to resolve claim payment barriers.
The Business Account Executive is responsible for driving disease awareness, patient identification, and brand growth within their assigned territory. They will collaborate with internal and external stakeholders to execute account strategies and achieve regional sales objectives.
The Associate Director will represent Clinical Pharmacology for CNS RNAi therapeutic projects and lead the analysis, interpretation, and reporting of clinical data. They will also provide critical input for regulatory submissions and collaborate across various R&D functions to guide clinical development decisions.
Lead enterprise-wide corporate environmental sustainability strategy and manage ESG disclosure compliance. Conduct life cycle analysis of products and manage internal sustainability projects in collaboration with facilities and capital project teams.
The role involves designing and executing real-world evidence studies and economic models to support the value proposition of pharmaceutical products. You will collaborate with cross-functional teams to generate insights from healthcare data and contribute to scientific publications.
The HR Business Partner will strategically partner with senior leaders to execute people strategies and drive business objectives within the commercial organization. They will also own organizational design, lead talent development initiatives, and act as a change management advisor to support high-growth field operations.
The Case Manager assesses patient needs to develop action plans for treatment initiation and maintenance while coordinating with internal and external stakeholders. They manage the reimbursement process, including insurance approvals, billing, and patient assistance programs to ensure seamless access to therapy.
The Associate Case Manager is responsible for verifying insurance coverage, managing patient referrals, and coordinating therapy access services. They also maintain accurate patient data, track specialty pharmacy referrals, and provide support to the broader Patient Services team.
The Senior Manager, Study Start-up leads global site activation and study start-up activities, ensuring predictable delivery through data-driven forecasting and CRO oversight. They also develop and implement processes to optimize clinical trial timelines and remove operational obstacles for site activation.
The Senior Manager is responsible for the strategic planning, development, and implementation of training programs for Market Access and Strategic Accounts teams. They will collaborate cross-functionally to ensure compliant delivery of training materials and use performance data to drive continuous improvement.
The Health System Medical Outcomes Science Liaison serves as a field-based scientific expert, engaging with formulary decision-makers and C-suite leaders to communicate the clinical and economic value of Alnylam's portfolio. They are responsible for developing account-specific strategic plans, identifying research collaboration opportunities, and supporting evidence-based decision-making within health systems.
The Principal Medical Writer leads the development of clinical documents and represents medical writing on multi-disciplinary teams. They are responsible for overseeing contract writers, ensuring regulatory compliance, and facilitating the review process for clinical documentation.
The Associate Director will lead the national strategy and execution for US congress presence and Thought Leader Liaison (TLL) marketing initiatives. This role involves managing cross-functional collaborations, overseeing KOL insight processes, and ensuring all educational content is scientifically accurate and compliant.
The Business Account Executive is responsible for identifying and targeting healthcare providers to increase brand awareness and product adoption for TTR amyloidosis treatments. They must build and maintain strategic relationships with physicians and internal stakeholders to achieve territory sales targets.
The Key Account Manager is responsible for developing and implementing strategic account plans to drive commercial objectives and optimize patient care within their assigned territory. They will manage relationships with healthcare professionals, identify treatment centers, and ensure the effective promotion of RNAi platform products.
Lead the multi-year roadmap and business ownership for Quality digital capabilities including SAP, Veeva, and LIMS. Act as the primary bridge between Quality and IT to translate business needs into scalable, compliant digital requirements and ensure data integrity.
The MSL is responsible for building scientific partnerships with KOLs and healthcare professionals to elevate disease understanding of TTR amyloidosis. They will deliver scientific information, gather medical insights, and support clinical trial patient accrual within the Ohio Valley geography.
Drive the operational excellence and effectiveness of customer-facing field teams across Commercial and Medical Affairs. Translate business strategies into actionable execution frameworks through KPI management, reporting, and field alignment.
The MSL will build scientific partnerships with key opinion leaders and healthcare professionals to elevate disease understanding of TTR amyloidosis. They are responsible for delivering scientific information, gathering medical insights, and supporting patient accrual for clinical trials.
The MSL will build scientific partnerships with key opinion leaders and healthcare professionals to elevate disease understanding of TTR amyloidosis. They are responsible for delivering scientific information, gathering medical insights, and supporting patient accrual for clinical trials.
The KAM is responsible for driving commercial objectives for ATTR treatments by developing and implementing strategic account plans in the Campania Nord and Molise territories. This includes identifying diagnosis centers, managing relationships with healthcare providers, and collaborating with Medical Affairs to optimize patient care.
