Amgen

Manager

• Responsible for research activities on the Inflammation therapeutic area team
• Recognized as a strong scientific contributor and a first or contributing author for papers in peer-reviewed journals
• Designing and performing studies to support evidence generation such as identifying appropriate patient populations
• Influencing cross-functional team members in the utilization and timing of non-interventional research
• Leveraging real-world data and analytic approaches to inform high-value business decisions
• Tracking business and functional priorities and aligning resources

Senior Manager, Observational Research – Inflammation

Director

• Report to the Executive Director, Precision Medicine/Dx and R&D Supplier Quality
• Provide leadership to a professional quality team
• Develop and implement an end to end, proactive and risk-based Quality Assurance strategy for Precision Medicine and Diagnostics
• Ensure compliance to an evolving and complex IVD regulatory landscape
• Develop collaborative partnerships with R&D Leadership to define the state of quality and potential areas of quality risk exposure
• Coordinate and collaborate with clinical trial teams to incorporate all respective critical to quality components into clinical trial design
• Maintain up-to-date knowledge of IVD regulations and applicable guidance
• Oversee the management of IVD-related QMS elements related to business procedures

Director, Precision Medicine and Diagnostics Quality

Data Analyst

• Own reporting and analytics related to the patient funnel, including enrollments, initiations, adherence, time-to-fill, treatment status, engagement, and drop-off points.
• Deliver clear, timely, and actionable insights to Brand POD (cross-functional analytics matrix team) to inform strategic and tactical decisions.
• Conduct ad hoc and deep-dive analyses to address complex patient access and reimbursement questions.
• Develop dashboards, recurring reports, and executive-ready presentations to support senior leadership discussions.
• Ensure data accuracy, quality control, and clarity of communication across all reporting outputs.
• Partner with cross-functional analytics teams to align on KPIs and deliver a cohesive “story behind the data.”
• Collaborate with Market Access analytics to assess payer coverage, reimbursement trends, and access barriers.
• Provide a comprehensive view of the patient journey, highlighting opportunities to optimize access, adherence, and patient experience.
• Manage and integrate multiple data sources (e.g., hub services, specialty pharmacy, claims, and internal data systems).

Patient Access Analytics Manager

• Join Amgen’s Mission of Serving Patients
• Drive transformation and build critical capabilities that enable Amgen to respond to rapid advancements in science and technology within a rapidly changing business environment
• Lead transformation programs or workstreams to deliver business solutions from problem-solving through implementation
• Conduct qualitative and quantitative analyses to elucidate opportunities
• Define KPIs and outcome measures (e.g., cost, quality, NPS) to monitor process health and set continuous improvement targets
• Facilitate alignment on case for change, vision, ambition targets and realization measures
• Lead a team to support transformation programs and/or lead workstreams
• Drive execution excellence on transformation programs by leading the development and management of the workstream roadmap, project schedule, and status reporting
• Liaise and coordinate across transformation and business teams and manage escalation of issues as needed

Director, Execution Excellence

Data Scientist

• accountable for the delivery of key AI/ML projects for the Data Science team within Amgen’s commercial organization
• Lead a team of data scientists to utilize advanced methodologies in AI/ML to craft and deploy bespoke solutions
• Leads execution and delivery for Machine Learning and advanced analytics projects overseeing capabilities for predictive modeling, AI/ML, Gen AI, and other large-scale data modeling projects
• Prototype and productionize advanced models using probabilistic time-series, deep learning, causal inference, reinforcement learning, agent-based simulation, and generative/agentic techniques
• Lead Omnichannel media strategy aligning with brand objectives and driving impact
• Provide day to day guidance for team of data scientists (both Sr and Jr members) in projects ranging from statistical analysis, predictive modeling and Generative AI
• Develops, coaches, leads, and retains a dynamic, high-performing Data Science team delivering results, and gaining trust with stakeholders
• Effectively communicates with key stakeholders on the impact, status and success of Data Science capability initiatives
• Provides Data Science capability through relevant data science certifications and Biopharmaceutical industry expertise and direction to the CD&A organization
• Maintain an awareness of current research and standard methodologies in the field of data analytics, including best practices in analytics
• Primary point of contact for Commercial leaders to engage in AI/ML activities
• Engages and communicates with key stakeholders on the impact, status and success of Data Science capability initiatives.

Associate Director, Commercial Data Science

Clinical Research

• support late-phase clinical development by contributing to protocol development, study start-up, data review and monitoring and analysis activities
• Working collaboratively with the study team and clinical leadership
• focus on study-level implementation and cross-functional coordination to help ensure high-quality, decision-ready clinical data
• Support set up and execution of late phase clinical trials with a focus on data quality
• Assist in authoring clinical protocols, Investigators Brochures and other regulatory documents ensuring consistency and clarity
• Provide input into and implementation of data management plan, CRF design, and data review oversight
• Support review, analysis, and presentation preparation of clinical trial data for internal decision making, external interactions, and regulatory submission
• Assists Development Lead and Clinical Scientist Director in medical monitoring and management of collaborators, consultants, and/or Clinical Research Organizations in completion of key projects
• Anticipate and actively manage problems across a broad spectrum of cross-functional teams
• Work cross functionally within teams to ensure clinical strategy is translated into the development of the study concept document, study protocol and related documents
• Support appropriate training, recruitment, and development requirements for matrix team resources.

Clinical Scientist Associate Director – Autoimmune/Inflammation

• Articulate and communicate a clear strategic vision for the TLL team, fostering a culture of performance, accountability, and continuous improvement.
• Establish and maintain strong relationships with the medical community by cultivating Key Opinion Leaders (KOLs) and product advocates across academic and community settings nationwide and within assigned geographies.
• Collaborate cross-functionally with medical, sales, and global teams to ensure consistent information exchange and alignment with organizational objectives.
• Oversee the development and execution of commercial KOL engagement plans, ensuring integration and alignment with sales, marketing, and leadership strategies.
• Maintain deep expertise in product, disease state, market dynamics, and reimbursement to inform strategic business planning and drive KOL engagement, product adoption, and leadership connectivity.
• Lead and motivate the TLL team by setting clear objectives, allocating resources effectively, and monitoring performance and activities.
• Recruit and develop top talent, ensuring team members possess the skills and capabilities needed to succeed in an evolving industry and therapeutic landscape through ongoing coaching and feedback.
• Identify and implement training opportunities to strengthen team capabilities in product and disease state expertise, account management, strategic planning, analytics, presentation skills, and marketing tool utilization.
• Proactively identify and address business or personnel challenges that may impact performance, provide coaching and implementing corrective actions as needed.
• Continuously assess talent and succession readiness to ensure a strong leadership pipeline within the team.
• Support the planning, coordination, and execution of major congress meetings and related engagements.
• Ensure compliant and effective management of speaker bureau activities and program implementation.

Associate Director, Thought Leader Liaison

• Support late-phase clinical development by translating scientific and clinical strategy into actionable execution across clinical trials
• 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.
• Work cross functionally to ensure clinical strategy is translated into the development of the study concept document, study protocol, and related documents
• Provide guidance and assistance in the identification and management of collaborators, consultants, and/or Clinical Research Organizations (CROs) in completion of key projects.
• 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.
• Ensure integrity of protocols and/or components of clinical plans and for the delivery of final protocol and its governance approval.
• Contribute to medical monitoring activities and support ongoing assessment of subject-level clinical data to identify trends, risks, and emerging issues.
• 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.
• Present information internally and externally, anticipating and actively managing problems across a broad spectrum of cross-functional teams.

Clinical Scientist Director – Late Development, Rare Disease

• Provide inputs, insights, and recommendations towards shaping and implementing our marketing strategies
• Analyze the performance of our commercial investments across sales, online and offline channels
• Provide analytical support throughout the investment lifecycle including sizing, experimental test design, measurement, optimization, and scenario planning
• Oversee a group of data scientists leveraging advanced statistical modeling techniques
• Develop a suite of Marketing Mix Models and Multi-Touch Attribution models
• Understand and influence key levers of business growth
• Design, implement, and analyze experiments and quasi-experiments
• Accountable for measurement of spend efficiency and make recommendations on optimization
• Collaborate with Marketing, Media, Finance and other Analytics teams to create marketing budgets
• Hire, coach, mentor and lead a team of analytical leads that deliver data-driven recommendations.

Data Science Director – Marketing Investment Analytics

Account Manager

• Responsible for representing Amgen's Rare Disease products to Primary Care/FP/GP/IM, Podiatry, and Orthopedic physicians and healthcare professionals
• Establishing Biotech/Infusion product sales
• Increasing referrals for appropriate patients to the Rheumatology and Nephrology specialties
• Performing total territory account management
• Work strategically and collaboratively across existing sales teams to uncover unmet needs in the uncontrolled gout patient population
• Providing account management support to accounts within a specific geography in the PCP, Podiatry, and Orthopedic marketplace
• Collaborating with 2-3 Specialty Account Managers in the Rheumatology and Nephrology sales teams to identify appropriate referral patients
• Developing a comprehensive and effective territory business plan aimed at achieving and exceeding annual sales goals established by commercial leadership
• Promoting Disease State awareness and value of product to target customers
• Communicating territory activity in an accurate and timely manner as directed by management
• Adhering to the Amgen’s compliance policies and guidelines and any other applicable guidelines

Account Manager – Rare Disease

Research Scientist

• Lead the strategy and execution of innovative bioanalytical platforms to measure antibody-siRNA conjugates in preclinical samples (in vitro and in vivo)
• Lead strategy to establish innovative in vitro ADME assays for antibody-siRNA conjugates
• Design, execute, and interpret results from in vivo studies characterizing pharmacokinetics, pharmacokinetic-pharmacodynamic relationships, tissue distribution, and toxicokinetics of antibody-siRNA conjugates
• PKDM-BA project team representative for antibody-siRNA conjugates and other siRNA modalities
• Lead and execute on preparation of the pharmacokinetic written summary for regulatory applications
• Mentor and cross-train PKDM-BA scientific colleagues
• Build and foster cross-functional collaboration across Research and Development to advance siRNA therapeutics from discovery to clinical proof of concept

Senior Principal Scientist – Antibody-siRNA Bioanalytical, Biodistribution Strategy Lead

Marketing

• Support the pull through of personal marketing programs and tactics
• Demonstrate ability to think strategically and creatively for impactful results
• Manage budgets and organize complex project work
• Partner to create program KPI goals and execute measurement plan
• Develop promotional material for the Key Account Management (KAM) team

Marketing Manager, HCP

• Act as Center of Excellence lead for Launch Sequence Optimisation (LSO) and International Reference Pricing (IRP) analytics
• Identify and mitigate cross-market reference price spillover risks across the portfolio
• Apply and monitor global pricing rules, managing deviations, escalations, and governance compliance
• Ensure consistency in price corridors, baskets, thresholds, and country rock-bottom (CRB) validations
• Analyze structural ASP erosion drivers and lead root-cause assessments (e.g., IRP, tenders, MEAs), recommending mitigation strategies
• Support quarterly price reporting, brand performance reviews, and enterprise planning cycles (Budget, LRP, Forecast)
• Contribute to the development of brand-level price defense, contracting frameworks, and rock-bottom principles
• Support the operationalization and continuous improvement of Global Price Governance processes

Global Operational Pricing Excellence Associate Director

Engineer

• Responsible for leading HFE/UE planning, research, development, and continuous improvement of Amgen drug delivery devices using HFE/UE best practices and in accordance with current regulations and guidelines within the medical device, combination product and bio-pharmaceutical industries.
• Partner cross-functionally with engineering, operations, regulatory, risk, quality, clinical, drug product, digital health, commercial to ensure Amgen products are safe and effective for end users.
• Lead and support human factors and usability engineering activities to improve the design of products, specifically the device-user interface.
• Develop, strategize, and implement a risk-prioritized, fit-for-purpose approach to HF activities.
• Ensure human-system capabilities and limitations are accurately reflected in the system requirements, and HFE/UE input is provided across functions to develop device design, packaging, labeling, and training requirements.
• Identify, lead, and support appropriate human factors and usability engineering activities to improve the design of device-user interfaces, including the device, packaging, labeling, and instructions for use to minimize the potential for use errors.
• Analyze objective and subjective data from usability studies to inform product design, identify and mitigate use-risk, and provide robust solutions.
• Lead the design and execution of human factors formative and summative activities, including moderation, note taking, vendor engagement, and analysis of data.
• Support and provide HFE expertise in preparation for clinical studies and regulatory submissions in accordance with HF best practices, guidance and standards.
• Create documentation to support development activities, design controls, DHF, DMR including protocols, task analysis, use-related risk analysis (URRA), usability technical assessments, HF validation reports, and regulatory submissions.
• Clearly and actively communicate regularly with key internal and external partners.
• This position requires up to 20% yearly travel mostly local and domestic.

Senior Human Factors Engineer – Usability

Program Manager

• Support Medical Program Management activities
• Interface with Global Medical Affairs team members
• Prepare agendas, capture meeting minutes, and document action items
• Maintain a program plan, meeting cadence, and milestone tracker
• Prepare clear written summaries and a final readout deck for stakeholders
• Support Precision Medicine Oncology and Digital Pathology collaborators