Amgen

General Counsel

• Develop, implement, and execute global intellectual property strategies for Amgen’s therapeutic products and product candidates (e.g., small molecules and peptides), related to, for example, compositions, polymorphs, formulations, processes, and methods of manufacturing.
• Working with Amgen scientists to identify patentable subject matter
• Drafting, filing, and prosecuting patent applications worldwide
• Conducting prior art searches
• Analyzing patents and preparing freedom-to-operate opinions
• Conducting due diligence in support of licensing activities
• Negotiating and drafting research agreements
• Providing legal advice and counsel to R&D and business partners on a variety of IP related matters
• Assisting with litigation-related matters and challenging/defending patents in PTAB, opposition, and other forums.

Senior Counsel – Patent Medicinal/Pharmaceutical Chemistry

Architect

• Be accountable for helping drive the successful design, architecture, build, test and implementation SAP S/4 Transportation management solution across all the Amgen manufacturing and distribution sites
• Partner with business leads, business engagement teams to support the development of business cases for delivering the IT roadmap and Business strategy
• Collaborate with Business, Operations IS and ERP solution architects (Order-to-Cash, Record to Report, Source to Settle) for cross functional integrations and E2E solution design
• Serve as solution owner for the SAP transportation management solutions within the global ERP architecture team
• Lead continuous improvements to drive IT effectiveness with the business and IT
• Collaborate with business and operations IS teams to identify future business needs and prioritize resources/effort to support the delivery of business-critical projects, enhancements and process improvements
• Deliver on portfolio investments and ensure business value outcomes are realized based on prioritized business needs
• Drive implementation of cross functional initiatives required for regulatory compliance
• Uses deep business knowledge to drive engagement on major IT initiatives
• Influence architecture decisions and solution choices with business stakeholders and enterprise architects
• Manage Implementation vendor to ensure the effective execution of the projects and services, holding them accountable to project scope, SLAs and critical metrics
• Drive configuration and development activities to meet business requirements through a combination of internal and external teams
• Ensure all the required functional, configuration and technical design documents of SAP TM capabilities are created in compliance with GxP requirements and ERP architecture standards
• Support Validation/QA teams on ensuring GxP compliance of SAP TM capabilities with the corporate standard for IT change management and IT SOPs following 21 CFR Part 11 and Annex 11 requirements
• Promotes adoption of SAP industry best practices within in S/4 transportation management and logistics execution workstream.

SAP Principal Architect, Transportation Management

Manager

• Handling industry leading transformation of overall patient support offerings
• Engaging directly with health care professionals and matrix partners to establish options for financial assistance / reimbursement
• Making outbound calls to health care professionals (HCPs), when required
• Entering data into supporting systems to initiate enrollment of new and existing patients
• Reviewing Patient Enrollment Forms for completeness and accuracy, identifying any potential barriers and following all processes outlined in SOP
• Initiating patient’s benefits verification by reviewing patient data and insurance material
• Ensuring that data entry process into the supporting system is completed accurately and in a timely manner
• Monitoring potential delays or pending cases

Intake Case Manager – Rare Disease

Director

• Lead a team of epidemiologists to conceptualize, design, conduct, analyze, interpret and publish observational research supporting drug development programs and regulatory submissions
• Identify evidence needs and develop the RWE plan to support product development and commercialization strategy
• Design and execute studies to support evidence generation such as identifying appropriate patient populations
• Find opportunities to substitute for and/or complement interventional studies to reduce time and cost of drug development
• Influence cross-functional team members regarding the appropriate use and timing of non-interventional research
• Leverage real-world data and CfOR analytic approaches to inform high-value business decisions
• Track business and functional priorities and align resources against those priorities
• Develop and maintain relationships with key leaders in observational research

Director, Observational Research – Obesity

Supply Chain

• Manage assigned end-to-end processes and ensure their readiness for execution of clinical supply chain processes.
• Partner with DTI to assist with the resolution of technical incidents utilizing the Integrated Service Management-ServiceNow (ISM-SN) application.
• Point of contact for application issues, incidents, and troubleshooting.
• Manage timely closure of incidents.
• Troubleshoot technical incidents with end users utilizing both internal resources and outside organizations such as External Trial Operations (ETO).
• Monitor iDoc failures and determine the root cause of issues.
• Work with the business and/or DTI team to implement corrective actions.
• Act as a change record owner to support continuous improvement initiatives.
• Manage documentation and maintenance of clinical customization requirements to support readiness for key projects, audits, and inspections.
• Manage audit readiness playbooks for assigned processes.
• Interpret customers’ needs to identify potential opportunities for improvements.
• Generate Business Requirements (BRD) documents to initiate enhancements per the intake process.
• Support development of business cases for proposed system enhancements.
• Support and/or lead enhancement implementation.
• Develop project milestones, adhere to timelines, utilize project management tools such as Smartsheet, communicate issues, ensure issue resolution, and ensure change management for business end users.
• Act as primary tester for system enhancements and upgrades, which includes script authoring/approval, data preparation, test execution, and defect resolution test approval.
• Support training in the clinical OTC and/or PTS process at Amgen to DSC and cross functional staff.

Supply Chain Manager – Development Supply Chain Technologies

• Achieve results through detailed goal setting, accountability measures, effective partnership, performance management, collaboration with other groups, and dedication to serving customers
• Independently lead sophisticated studies in the General Medicine therapeutic areas ensuring statistical aspects of clinical activities meet required standards and are robust and valid
• Influence and supply to strategy development
• Defend statistical approaches
• Represent GBS through participating in and collaborating with multidisciplinary study teams

Biostatistics Manager, General Medicine

Engineer

• Own and manage Citrix Virtual Apps and Desktops infrastructure, ensuring performance, availability, scalability, and compliance.
• Administer and maintain Citrix ADC (NetScaler) environments, including: Global Server Load Balancing (GSLB)
• Load Balancing services
• Content Switching policies
• SSL offloading and certificate management
• Web Application Firewall (WAF)
• Multi-factor authentication (MFA) using nFactor authentication policies
• Maintain the health and resiliency of Citrix environments, including Citrix Cloud and Citrix ADC platforms.
• Design and implement secure remote access solutions leveraging Citrix Gateway and advanced authentication integrations.
• Perform patching, firmware updates, and platform upgrades in line with enterprise change management policies.
• Troubleshoot and resolve complex technical issues involving Citrix infrastructure, user sessions, authentication flows, networking, and backend integrations.
• Serve as the technical escalation point for Citrix and NetScaler-related incidents within IT operations.
• Collaborate with network and security teams to implement enterprise traffic management and application delivery strategies.
• Document configurations, SOPs, architecture decisions, and operational runbooks to support audits and operational continuity.
• Monitor system alerts, identify systemic issues, and implement long-term corrective and preventive actions.
• Mentor support teams and transfer knowledge to ensure consistent operational support coverage.

IS Engineer – Citrix Specialist

• support early-phase clinical development by translating scientific and clinical strategy into actionable execution across clinical trials
• Provide hands-on oversight of protocol execution, medical data review, and clinical data quality to enable high-quality, decision-ready data
• work collaboratively within cross-functional teams to ensure clinical trials are executed in alignment with protocol intent, regulatory expectations, and Amgen quality standards
• Serve as a clinical and scientific subject-matter expert for the assigned therapeutic area and disease indication, with a strong focus on protocol execution and data integrity
• Contribute to medical monitoring activities and support ongoing assessment of subject-level clinical data to identify trends, risks, and emerging issues
• Present information internally and externally, anticipating and actively managing problems across a broad spectrum of cross-functional teams
• Provide guidance and assistance in the identification and management of collaborators, consultants, and/or Clinical Research Organizations (CROs) in completion of key projects
• Work cross functionally to ensure clinical strategy is translated into the development of the study concept document, study protocol, and related documents
• Ensure integrity of protocols and/or components of clinical plans and for the delivery of final protocol and its governance approval
• Provide clinical input into & implementation of clinical trial(s), delivery, clinical data review, and interpretation of results
• Review and analyze clinical trial data to ensure accuracy, completeness, and adherence to protocol and regulatory requirements
• Conduct thorough data quality assessments in the context of a data monitoring plan to maintain high standards of data accuracy and integrity throughout the trial lifecycle

Clinical Sciences Director – Early Development, Oncology

Security Engineer

• own global QMS processes for Warehousing & Distribution (W&D) and Supply Chain Security (SCS), ensuring standardization and consistency across the network.
• Define, maintain, and continuously improve global QMS processes for W&D and SCS, including standards, process flows, and documentation.
• Assess and implement changes to processes to meet evolving regulatory, compliance, and business requirements.
• Establish and manage process governance, including metric frameworks, performance tracking, and reporting.
• Monitor process performance, analyze trends, and identify risks or gaps requiring corrective or preventive actions.
• Lead and execute CI and OE initiatives across the GSC network.
• Own and manage business systems supporting QMS processes (e.g., lane management, distribution complaints), including enhancements and lifecycle oversight.
• Manage supplier-related processes for distribution materials to ensure quality, compliance, and performance standards are met.
• Lead cross-functional collaboration to align processes and improve E2E performance.
• Plan and support audits and MRs, ensuring processes meet quality expectations.
• Drive change management activities related to process and system updates, ensuring adoption across regions and functions.

Global Process Owner – Warehousing, Distribution & Supply Chain Security

Sales

• Track the progress of marketing messages and programs
• Provide feedback to district teams on the marketing, allocating, monitoring, and leveraging of internal and external resources (e.g., discretionary spend)
• Manage district teams to maximize their performance and help achieve/exceed sales and budget targets
• Screen, interview, and hire candidates
• Ensure compliance with training
• Demonstrate the appropriate coaching and counseling to prepare individuals for future development
• Conduct annual and on-going performance reviews and competency assessments
• Communicate and coordinate with both district and cross-functional teams (e.g., Marketing, Finance, other Business Units)
• Share best practices with direct reports and peers
• Coordinate and/or participate in cluster teams
• Conduct district sales meetings to guide districts
• Develop local Opinion Leader relationships to achieve aligned objectives

District Sales Manager – Respiratory Biologics

• In this vital role you will work in close partnership with the National Sales Director to achieve strong sales force delivery in alignment with Brand strategy.
• This is primarily achieved by identifying unique performance and delivery trends as well as geo-specific opportunities, using data to fully characterize these as well as to assess progress over time.
• The NBM enables enhanced focus for both the NSD as well as RSDs in terms of coaching, development, Opinion Leader engagement, etc.
• Support NSD in aligning national direction with brand and corporate strategy.
• Interpret data and trends within specific geographies in order to highlight specific brand performance opportunities.
• Provide analytical support in identifying local business opportunities, assist in outlining tactics, and provide any critical metric support needed to assess progress.
• Partner with SPO to suggest changes to analytic tools to simplify information to improve usage and effectiveness as needed.
• Use analytics to see opportunities and create pull through strategies for new wins or changes in coverage.
• Maximize Vision reporting tools to monitor pull-through progress and opportunities.
• Monitor MMIT utilization and work to optimize delivery.
• Monitor co-pay utilization and share relevant insights.
• Partner with region leadership team to optimize RAS, vRAS, and OPM/RAS program deployment.
• Actively investigate data and IC inquiries to help maintain credible compensation data.
• Have direct conversations with the field on data questions and concerns.
• Partner with NSD/SPO to ensure field understanding of the plan and develop strategy to demonstrate IC, special incentives, contests, as performance drivers.
• Ensure region payouts are enhanced through periodic opportunity assessments and effective communication/motivation.
• Partner with the NSD/SPO to develop a national engagement plan (Nation Calls, skip levels, leadership team calls, ACT III engagements, etc).
• Partner with NSD/SPO to create any PowerPoint content and seek internal approvals (if required).
• Serve as contact for x-functional partners such as FTM, RAS lead, VSP DM, as well as key OLs and Speakers in the Region.
• May provide Interim District Manager coverage when there is a vacancy or leave.
• Assist in recruiting and hiring process for the Nation.
• Partner with SPO to gain expertise as regional expert in field processes including Veeva, Sampling, Speaker programs, Congresses, etc.

Regional Business Manager – Cardiovascular

Product Operations

• Help establish, scale, and continuously improve Amgen’s Digital Product Operating Model (DPOM) across the enterprise
• Own the operating infrastructure that enables Amgen’s shift from projects to products, including the DPOM playbook, product management standards, enterprise tooling strategy, adoption measurement, and integration of product ways of working into core business, technology, finance, agile, and governance rhythms
• Translate product management principles into practical, repeatable systems that teams across Amgen can understand and adopt
• Create and maintain the DPOM playbook as a trusted enterprise resource
• Define how product practices, decision rights, lifecycle standards, OKRs, roadmaps, portfolio planning, intake, documentation, and measurement work in practice
• Lead research and recommendations for digital tools that support DPOM
• Evaluate options, align stakeholders, present recommendations to leadership, and drive adoption of selected tools across the enterprise
• Own the enterprise measurement system for DPOM adoption, maturity, and effectiveness
• Define metrics, maturity indicators, and reporting mechanisms that show how product ways of working are being adopted across product groups and business functions
• Partner closely with stakeholders to embed DPOM into enterprise-wide cadences.

Director, Digital Product Operations

• The Computational Biology group in the Center for Technology and Innovation (CfTI) within the Precision Medicine organization is seeking a highly motivated Computational Biologist with expertise in analyzing clinical biomarker data
• This role will contribute to advancing clinical programs and studies by integrating computational biology and bioinformatics techniques with biological and clinical data
• Support CVMet and OaR teams as a CompBio Therapeutic Area Lead and Global Biomarker Analysis Lead
• Develop biomarker analysis plans to support precision medicine, evidence generation and reverse translation during clinical development of therapeutic molecules
• Define and execute workflows for biomarker data analysis, integrating multiple omics, imaging and digital biomarkers, integrated with clinical metadata and outcomes
• Lead the analysis and interpretation of clinical biomarker data from various assay platforms
• Support the generation of evidence for target engagement evaluation, patient stratification, response prediction, indication selection, assay development, and diagnostic development
• Collaborate cross-functionally with early development teams, biostatistics, clinical pharmacology, precision medicine leads, clinical biomarker leads, and research teams to manage data integration, analysis, and presentation
• Support internal and external presentations with fit-for-purpose analysis insights and messaging and support the development of publications

Associate Director – Computational Biology, Cardiovascular, Metabolic, Obesity and Related

Product Manager

• Lead a team of product managers who embed with priority products, product groups, and enterprise initiatives
• Accelerate Amgen’s adoption of the Digital Product Operating Model (DPOM)
• Help Amgen move from output-driven delivery to outcome-driven product management
• Perform product management responsibilities while embedded with teams, including clarifying user and business problems, shaping product strategy, improving roadmaps, defining OKRs and KPIs
• Support teams in developing strong product strategies, roadmaps, OKRs, KPIs, discovery practices, and value realization plans
• Partner with business functions, digital product leadership, and technology leaders to align product work to enterprise priorities and measurable business value.

Director, Digital Product Management

Compliance

• Support the integrity, accuracy, and compliance of key reports and SAP GRC controls relied upon for SOX processes
• Serve as a key contributor to the SOX Key Reports program, supporting reports relied upon for SOX controls
• Perform detailed technical analysis of report logic, including code, queries, scripts, and data transformations, to understand how reports are generated
• Validate report completeness and accuracy by reconciling report outputs to source systems and underlying data
• Assess report logic and calculations to confirm alignment with control objectives and SOX requirements
• Partner with system owners and developers to review report design, logic, and dependencies
• Perform report tie-outs between the report provided by the process owner and the independently generated output derived from code or query review
• Recreate report outputs using reviewed SQL queries, application logic, or ERP report code to validate accuracy
• Confirm report logic, parameters, and date ranges used by the process owner align with the underlying code reviewed
• Investigate, document, and resolve variances identified during tie-outs, ensuring explanations are reasonable, supported, and appropriately approved
• Analyze and interpret technical artifacts such as SQL queries, stored procedures, ETL logic, and application code as needed
• Ensure key reports meet SOX documentation and testing requirements, including report completeness, accuracy, and change management controls
• Support internal and external audits by providing technical explanations, reconciliations, and evidence related to SOX key reports