Amgen

Medical Director

• Collaborate with multiple cross-functional teams to shape global strategic direction for multi-channel medical and scientific external engagement throughout the lifecycle of therapeutic area (TA) products
• Responsible for driving engagement excellence with key external organizations to optimize Amgen’s strategic objectives
• Supports the design and delivery of a comprehensive global external medical and scientific engagement strategy across external stakeholders (congresses, cooperative groups, and societies)
• Develop the annual global oncology and hematology congress strategy, ensuring cross-functional alignment, prioritization, and budget stewardship across regions (ELMAC, JAPAC, US)
• Oversee execution to ensure alignment with medical objectives, consistent communication, and streamlined reporting
• Collaborates with cross-functional teams, regional leads, TA Heads and R&D leadership, as well as Commercial and Access partners to ensure strategic alignment with external groups to achieve successful execution of medical initiatives and deliverables
• Defines and supports external engagement needs and opportunities within the global medical engagement strategic plan based on area of responsibility; executes the final global medical engagement strategic plan via interactions with both internal and external stakeholders in partnership with medical leads
• Partners with Field Medical to develop a comprehensive, cross-functional view of key Opinion Leader (OL) congress interactions to enhance strategic prioritization and support delivery of high-quality, strategic insights
• Provides strategic alignment with Commercial and Access teams on Value Based Partnerships at a platform/TA level
• Ensures capture, analysis, and distribution of scientific insights; forecasting scientific trends from opinion leader networks, cooperative groups, and/or professional societies; distributing internally to broaden awareness
• Integrate AI-driven solutions and champion AI adoption across medical engagement, congress planning, stakeholder management, and operational workflows to enhance efficiency, insights, and strategic impact
• Manages consistent communication with internal and external stakeholders to ensure alignment of strategic objectives to ensure successful outcomes
• Maintain an active role within TA medical team meetings to ensure awareness of potential opportunities for external engagement

Medical Director, Congresses & Partnerships Lead

Financial Planning and Analysis

• Act as a trusted advisor and force multiplier to senior leadership, driving alignment, execution, and measurable business outcomes
• Serve as a strategic advisor and extension of the SVP of Engineering
• Orchestrate priorities, decision-making, and alignment across the Engineering Senior Leadership Team (ELT)
• Own and continuously improve the Engineering operating rhythm, including ELT meetings, strategy sessions, and executive forums
• Lead development of CEO staff, Board of Directors, and external-facing materials
• Ensure effective governance frameworks that enable speed, clarity, and accountability
• Translate strategic priorities into actionable roadmaps and measurable outcomes
• Drive enterprise-wide transformation initiatives that improve performance, scalability, and resilience
• Identify and implement opportunities to improve productivity, capital efficiency, and operational performance
• Structure ambiguous problems into clear workstreams and drive execution to results
• Manage multiple high-priority initiatives simultaneously while maintaining quality and speed

Strategic Planning & Operations Director

Account Manager

• Develop and execute a comprehensive territory business plan to achieve and exceed sales objectives, aligned with broader commercial and strategic account goals.
• Promote KRYSTEXXA within approved labeling in a fair, balanced, and ethical manner in accordance with corporate and industry compliance guidelines.
• Serve as a trusted partner and disease expert to healthcare professionals by delivering meaningful, patient-centered education on disease state and product information.
• Build and manage strong relationships with a range of stakeholders across the patient care ecosystem—including physicians, nurses, office staff, case managers, infusion centers, and caregivers.
• Navigate and engage within diverse healthcare delivery settings such as private practices, academic institutions, IDNs, community hospitals, and specialty clinics.
• Identify and address patient access, reimbursement, and pull-through challenges by working cross-functionally with field access teams, patient services teams, and case managers.
• Coordinate internal matrix teams (e.g., MSLs, Market Access, Nurse Educators, TLLs) to deliver integrated, account-specific solutions that drive long-term customer engagement and product utilization.
• Lead or support the development of referral networks and site-of-care pathways to enable seamless patient initiation and continuity of care.
• Establish productive relationships with local and regional KOLs to expand reach and influence within the therapeutic landscape.
• Actively contribute field insights and market intelligence to cross-functional partners and leadership to inform strategy, resource deployment, and future planning.
• Leverage approved tools, peer education programs, and digital engagement channels to extend reach and increase impact with key stakeholders.
• Maximize use of promotional resources and operate within assigned territory budget to support business objectives.
• Represent the company at appropriate medical congresses, society meetings, and educational events to maintain therapeutic and competitive knowledge.
• Complete all training and administrative responsibilities in a timely and accurate manner while upholding all company policies and compliance standards.

Account Manager – Rare Disease

Security Engineer

• Play a pivotal role in developing and executing strategies to counter emerging threats to Amgen products throughout the regulated supply chain
• Direct response and remediation activities related to global supply chain incidents, including diversion and theft
• Collaborate across Amgen’s diverse internal network to ensure effectiveness and agility of the Product Security program
• Provide strategic oversight and support to global supply chain product security initiatives in partnership with Supply Chain Security and Operations
• Support a cross-functional steering committee, including representatives from Global Security, Operations, Supply Chain, Legal, and Corporate Audit
• Define and operationalize strategies for threat monitoring, incident reporting and response, enforcement protocols, and other key security functions
• Support the development of tools and systems used to monitor security threats impacting the supply chain
• Leverage the Global Security Operations Center (GSOC)
• Provide Amgen leadership with metrics, KPIs, and reports on emerging and ongoing threats to Amgen products
• Create and execute strategies to promote education and awareness of Product Security issues affecting Amgen
• Accountable to represent Amgen interests in industry and government working groups, task forces, and committees (e.g., PSI, HDA)
• Facilitate security audits of vendors, suppliers, and business partners, both proactively and in response to specific concerns
• Manage activities related to the supply chain security audit program, in collaboration with internal stakeholders
• Assess site risks and vulnerabilities for product security and create response plans to maintain effective security procedures
• Build and maintain relationships with law enforcement and emergency services agencies
• Coordinate efforts with other directorates within Global Security
• Select, train, and manage contract workers and consultants
• Conduct and manage internal and external investigations as needed.

Senior Manager, Product Security

Director

• Be responsible for the development, characterization, scale‑up, and support of drug substance cell culture and purification processes
• Lead and develop a multi-site organization of 30+ scientists and engineers
• Drive program success, safety culture, technical excellence, innovation, automation, and digital strategies.
• Support a diverse portfolio of biologics, including monoclonal antibodies (mAbs), BiTEs, bispecifics, biosimilars, and other novel protein‑based modalities
• Advance late-stage and commercial drug substance strategies across Amgen’s manufacturing network.
• Lead a high‑impact, multi‑functional drug substance organization integrating cell culture and purification disciplines across multiple sites.
• Recruit, develop, and retain a strong and diverse team; manage portfolio prioritization and organizational resourcing.
• Advance integrated drug substance processes through commercial process development, process characterization, lifecycle management, and control strategy development.
• Partner with engineering, manufacturing, and external network collaborators to enable successful process transfer and commercialization.
• Author and review global regulatory filings (IND/INDa/MA) and respond to regulatory agency questions.
• Drive ideation, development, and deployment of innovative and differentiating bioprocess technologies.
• Contribute to Amgen’s scientific and regulatory eminence through publications, patents, and participation in external conferences and forums.
• Serve as a member of the Drug Substance Technology extended leadership team and contribute to business, organizational, and change‑management strategies.

Director, Bioprocess – Process Development

Clinical Research

• In this vital role, the Clinical Scientist Associate Director will support the execution of cardiovascular trials by translating scientific and clinical strategy into high-quality study delivery across global, complex, late-stage clinical trials.
• The Clinical Scientist serves as a key clinical development team member, providing hands-on oversight of protocol execution, medical data review, endpoint quality, and cross-functional issue resolution to enable timely, decision-ready data.
• This role works collaboratively across clinical, medical, operational, data management, safety, and regulatory teams to ensure studies are conducted in alignment with protocol intent, study timelines, regulatory expectations, and Amgen quality standards.
• Serve as a clinical and scientific subject-matter expert for cardiovascular trials, with deep understanding of cardiovascular disease, endpoint strategy, protocol execution, and data integrity.
• Contribute to medical monitoring activities and support ongoing review of subject-level and aggregate clinical data to identify safety signals, endpoint trends, protocol deviations, and emerging operational or scientific risks.
• Present information internally and externally, anticipating and actively managing issues across a broad spectrum of cross-functional stakeholders, governance bodies, and external partners.
• Provide guidance and oversight in the identification and management of collaborators, consultants, adjudication vendors, and/or Clinical Research Organizations (CROs) to support successful trial delivery.
• Work cross-functionally to translate clinical strategy into study concept documents, protocols, endpoint definitions, charters, data review plans, and other key trial documents required for CV trial execution.
• Ensure the scientific and operational integrity of protocols and clinical plans, including delivery of final protocol content and governance approvals for large, global, event-driven studies.
• Provide clinical input into study startup, trial conduct, enrollment oversight, endpoint ascertainment, adjudication readiness, data review, and interpretation of results.
• Review and analyze clinical trial data to ensure accuracy, completeness, consistency, and adherence to protocol, endpoint definitions, and regulatory requirements, with strong focus on MACE and other cardiovascular outcome measures where applicable.
• Lead thorough data quality assessments in the context of a data monitoring and review plan to maintain high standards of endpoint reliability, safety oversight, and inspection readiness throughout the trial lifecycle.

Associate Director – Clinical Scientist, Cardiovascular Trials

Operations

• Lead, manage and co-ordinate the conduct of clinical trials from study start-up to close out (CSR/Archival) at a country level in accordance with ICH-GCP and other applicable local regulations
• Maintain the quality and scientific integrity of clinical trials at a local/country level
• Actively collaborate with cross functional internal and external partners to ensure timely delivery, budget implementation of clinical trial results within the local country
• Partner with global and local country teams to provide high level country strategy and actively drive study progress and local/country level study delivery
• Communicate country status (including timelines and results) to key partners including updates to relevant systems for transparency
• Provide country level input into the Country Operational Plan and partners with the Development Feasibility Manager through feasibility and with the Global Clinical Managers to ensure local delivery of the study
• Support internal audit and inspection activities and contribute to CAPAs, including leading resolution of issues when appropriate e.g., vendor management
• Assign and deliver all study support staff and continually review country level risk mitigation to ensure study delivers to plan

Local Study Operations Manager

• Provide strategic and operational support to Early Development Oncology Therapeutic Area
• Partner closely with the VP, Global Early Development
• Support Early Development leadership in strategy development, goal setting, and execution of organizational plans
• Advise the Early Development Head on priorities, progress, risks, and gaps, synthesizing insights to inform decisions
• Represent the business strategy for the Function and collaborate with Human Resources (HR), Finance, Corporate Communications to advance key objectives
• Lead complex, cross-functional initiatives, translating ambiguous business needs into actionable plans and delivering high-impact outcomes
• Operate effectively in a dynamic environment, managing ambiguity, ad hoc requests, and shifting priorities with independence
• Lead budget and resource planning, including forecasting, tracking, and alignment with global processes; oversee resource modeling and forecasting assumptions
• Manage headcount planning and approvals, partnering with HR on recruiting, onboarding, and talent management
• Develop dashboards, reports, and executive-level presentations to track performance and inform decisions
• Build strong partnerships across Global Development SP&Os and across R&D functions/ departments to drive alignment and best practice sharing
• Lead or represent the function in process improvement initiatives, advancing operational efficiency and consistency

Senior Strategic Planning & Operations Manager

Translator

• Develop and apply advanced computational methods to enable target discovery, validation, and biomarker identification across multimodal datasets
• Integrate diverse biological data types, including bulk, single-cell, and spatial omics
• Identify cell-type-specific and disease-relevant targets and characterize their cellular context
• Characterize gene function, pathway dependencies, and mechanisms of action
• Develop and apply computational frameworks for variant-to-gene-to-function inference
• Translate computational analyses into clear, testable biological hypotheses
• Collaborate closely with experimental scientists, computational biologists, and cross-functional teams
• Drive digital innovation by identifying gaps in analytical workflows and developing robust solutions.

Senior Scientist – Computational Discovery, Translational Analytics

Research Scientist

• Serve as a core toxicology and nonclinical safety representative on project teams, providing scientific leadership and regular updates to teams and management.
• Design, implement, manage and interpret nonclinical safety assessment programs in support of drug development candidates.
• Originate novel study designs and protocols to address complex scientific questions and develop integrated strategies to achieve project goals.
• Critically evaluate and interpret experimental data and author key sections of internal governance documents, INDs, BLAs, NDAs and other regulatory documents.
• Coordinate and collaborate with internal Amgen scientists and external partners to advance research and development programs.
• Participate in licensing, due diligence, and external partnering activities, as appropriate.
• Mentor and support other Amgen scientists in the design execution and oversight of nonclinical studies.
• Represent Amgen on nonclinical safety topics in interactions with U.S. and international regulatory agencies, and contribute to external industry initiatives aimed at advancing drug safety assessment paradigms.

Senior Principal Scientist – Project Toxicologist

Compliance

• Strengthen and advance Amgen's R&D Quality Management System (QMS) and Safety & Medical Quality (SMQ) competencies
• Lead Safety and Medical Quality processes with focus on labelling and regulatory affairs activities
• Responsible for leading processes related to pharmacovigilance (GPvP) annual audit plan, preparation and execution of audits, and monitoring of Quality events
• Act as the Quality Lead contact for Labelling & Regulatory Affairs activities within R&D Quality
• Assess and manage risks, including providing input into the annual GPvP audit plan
• Prepare, analyze, and communicate compliance metrics and other significant compliance information
• Maintain knowledge of current regulatory and compliance practices/issues and advise customers
• Develop long-term remediations and process improvements through Root Cause Analysis (RCA)
• Improve R&D processes by contributing expertise in identifying robust Corrective and Preventive Action plans (CAPA) and Effectiveness Verifications

Senior Quality Compliance Manager – Labelling & Regulatory Affairs

Digital Marketing

• Lead the planning and implementation of Ultra-Rare Brand Strategies into digital means
• Responsible for all Healthcare Professionals (HCPs) and consumer digital promotions supporting Ultra-Rare Brands in the U.S.
• Translate brand strategy into reality and guide Ultra-Rare towards the best possible outcomes
• Own end-to-end digital marketing tactics for Ultra-Rare, from creative brief, message development through execution, measurement, and optimization in partnership with Brand Marketing Leads and Brand Operations Manager
• Serve as a key partner to brand leadership by turning strategic goals into actionable projects
• Work closely with cross-functional teams including commercial, analytics, regulatory, compliance, and vendors
• Support brand strategy execution by promoting analytics and automation tools
• Convert brand objectives into measurable KPIs and SLAs
• Maintain all current established Ultra-Rare brand and unbranded websites
• Design and oversee strategies for digital media activation, re-activation, and prevention of discontinued engagement
• Help enhance and broaden a strong, data-driven marketing plan to engage healthcare professionals (HCPs)
• Manage daily relationships with agencies and publishers
• Advocate for ongoing innovation and continual learning.