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Amgen is a leading independent biotechnology company focused on developing innovative human therapeutics to address serious illnesses. Founded in 1980, Amgen leverages advanced human genetics and biologics manufacturing expertise to improve health outcomes and enhance the quality of life for patients worldwide.

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🏢 Careers

🏢 Amgen

💰 $28,500,000,000 Post-IPO Debt about 2 years ago🫂 Last layoff over 1 year agoBiotechnology Research

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🏢 Careers

Jobs at this company:

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🔥 Medical Sciences Director, Obesity/Cardiovascular - US, Remote

Posted about 20 hours ago

📍 United States

💸 211263.0 - 251266.0 USD per year

🔍 Pharmaceutical

🔧 Requirements

Doctorate degree and 4 life sciences/healthcare experience OR Master’s degree and 7 life sciences/healthcare experience OR Bachelor’s degree and 9 years life sciences/healthcare experience
5 years of pharmaceutical clinical drug development experience
Strong communication & presentation skills to clearly communicate scientific concepts/data to leadership committees both internally or externally (both written and oral)
Experience with designing, monitoring, and implementing clinical trials and interpreting test results in compliance with Good Clinical Practice standards and regulatory requirements
Understanding of conducting study data readout activities, including data cleaning, data base lock, data extract, producing outputs of data
Experience drafting high level submission documents for regulatory submissions including authoring clinical regulatory responses for health regulatory interactions
Serving as a contributing author to scientific publications and data presentations at scientific conferences
Experience in clinical data analysis such as Spotfire or other data analysis tools

💡 Responsibilities

Work cross functionally within teams to ensure clinical strategy is translated into the development of the study concept document, study protocol and related documents
Provide clinical input into & implementation of clinical trial(s), their delivery, clinical data review, interpretation of results.
Review and analyze clinical trial data to ensure accuracy, completeness and adherence to protocol and regulatory requirements
Support medical monitor in clinical trials and assist in resolving issues that may arise
Conduct thorough data quality assessments 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
Provide guidance and assistance in the identification and management of external collaborators, consultants, and/or Clinical Research Organizations (CROs) in completion of key projects

Data AnalysisData management

Posted about 20 hours ago

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🔥 Director of External Research and Development, Cardiometabolic/Obesity

Posted about 20 hours ago

📍 United States

💸 194497.0 - 230061.0 USD per year

🔍 Biopharma

🔧 Requirements

Doctorate degree in a scientific field
4 years of experience in drug development industry and/or biopharma business development
Strong leadership, scientific, organizational, communication, and project management skills
Excellent presentation skills

💡 Responsibilities

Lead Amgen’s business development efforts in identifying and evaluating innovative therapeutics being developed outside of Amgen within the cardiovascular and metabolic therapeutic space for potential in-licensing, M&A, or collaborations
Develop and nurture a network of key industry and academic contacts
Lead the technical evaluations of opportunities by creating and managing cross-functional review teams, providing recommendations based on robust scientific and drug industry knowledge, and ensuring appropriate and efficient decision-making processes
Engage in business negotiations and work with legal to execute contractual agreements for certain projects
Lead strategic discussions and presentations, collaborating closely with senior management, R&D, and Commercial
Mentor any direct reports

LeadershipProject ManagementBusiness AnalysisBusiness DevelopmentData AnalysisPeople ManagementCross-functional Team LeadershipCommunication SkillsMentoringNegotiationSales experienceStrategic thinking

Posted about 20 hours ago

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🔥 Product Manager - Pharma Contracts Management - US Remote PST

Posted 3 days ago

📍 United States

🧭 Full-Time

💸 162668.0 - 195836.0 USD per year

🔍 Information Systems

🔧 Requirements

6+ years in software product management/development
Experience with Salesforce Service Cloud, Conga CPQ, Conga CLM
2+ years managing teams or leadership experience

💡 Responsibilities

Manage multiple product teams for software applications on Salesforce
Lead technology strategy for market access and contracting
Create and manage product roadmaps for technology solutions

AWSLeadershipAgileProduct ManagementSalesforceDevOps

Posted 3 days ago

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🔥 Medical Value and Implementation Science (MVIS) Manager - Health IT Liaison Team- South Central US

Posted 13 days ago

📍 United States

💸 123189.0 - 152776.0 USD per year

🔍 Pharmaceutical/Biotech

🔧 Requirements

Strong eye for business, analytical skills, and critical thinking ability
Experience in pharmaceutical/biotech industry
Good understanding of IDNs and key partners
Understanding or familiarity of EHR systems within IDNs
Interest in population health management and implementation science
Experience successfully managing and motivating direct reports

💡 Responsibilities

Work with cross-functional medical and commercial account teams to gather customer insights and assess opportunities
Manage the customer accounts prioritization process for the MVIS Health IT Liaisons
Partner with Medical and IDN Strategy Team leads and other cross-functional partners to ensure alignment
Effectively assist through training and communication MSLs and KAMs on MVIS Health IT Liaison and EHR programs and resources and provide support to field staff to address questions
Deliver insights related to EHR objectives to key internal partners to help inform strategic decisions
Confidently engages customers in a field facing capacity using appropriate methods and MAC approved materials/messaging
Demonstrates effective use of CRM tool to manage territory schedule and call documentation
Support cross-functional workstreams to support business initiatives as requested
Evolve future MVIS Health IT Liaison strategic and executional plans aligned to overall medical and brand strategic plans
Provide feedback and support on targeting strategies, Key Performance Indicators, and POAs

LeadershipProject ManagementCross-functional Team LeadershipStrategic ManagementCommunication SkillsAnalytical SkillsRelationship buildingCritical thinkingAccount Management

Posted 13 days ago

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🔥 Global Safety Director, Obesity – US, Remote

Posted 14 days ago

📍 United States

🧭 Full-Time

💸 184901.0 - 233959.0 USD per year

🔍 Bio/pharmaceutical

🔧 Requirements

Product safety in the bio/pharmaceutical industry or regulatory agency
Expertise in Obesity, Metabolic/CV therapeutic area, or clinical training
Experience with marketed product safety; risk management
Experience with phase 1-3 clinical trials safety assessments and analyses
Drug Submission experience
Leadership experience of the safety profile of products assigned with cross-functional team members.

💡 Responsibilities

Validate safety signals and lead safety signal assessments
Develop and maintain Core Safety Information (core data sheet, core risks in informed consent forms, etc.)
Prepare/review core and regional risk management plans including additional risk minimization measures
Prepare/review safety sections of periodic aggregate reports
Provide safety input to protocols, statistical analysis plans, and clinical study reports
Prepare/review safety sections of new drug applications and other regulatory filings
Serve as safety expert on Evidence Generation Team for assigned products
Inspection Readiness

LeadershipProject ManagementAgileData AnalysisSAPCross-functional Team LeadershipCommunication SkillsAnalytical SkillsProblem SolvingTime ManagementComplianceMS OfficeTeamworkRisk ManagementStrategic thinking

Posted 14 days ago

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🔥 Supply Chain Senior Manager - Global Supply Chain Leader- US Remote

Posted 17 days ago

📍 United States

🧭 Full-Time

💸 138134.0 - 162014.0 USD per year

🔍 Biotech

🔧 Requirements

Doctorate degree with 2 years or Master's with 4 years or Bachelor's with 6 years or Associate's with 10 years or High school diploma with 12 years of Supply Chain experience
7+ years experience in global pharmaceutical or biotech
Excellent communication skills

💡 Responsibilities

Provide thought leadership for lifecycle management and product strategies
Drive supply risk mitigation strategies
Supervise commercial supply planning
Map Value Stream for commercial products
Lead discussions with manufacturing and finance

Operations ManagementFinancial analysis

Posted 17 days ago

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🔥 Global Marketing Director, General Medicine, Cardiometabolic

Posted 25 days ago

📍 United States

💸 205879.0 - 243680.0 USD per year

🔍 Biopharmaceutical

🔧 Requirements

Doctorate degree and 4 years of marketing experience OR Master’s degree and 7 years of marketing experience OR Bachelor’s degree and 9 years of marketing experience
5+ years of pharma cardiometabolic experience
8+ years of experience and a track record of success in a series of commercial roles of increasing scope, scale and complexity, with leading companies in the biopharmaceutical industry, preferably in the cardiometabolic therapeutic area
Prior experience assessing and launching innovative cardiometabolic products
Experience in biotech/pharmaceutical marketing and promotions
Experience in global commercial and/or strategic regional roles of increasing scope, scale, and complexity
Demonstrated record of strong commercialization planning and pull through

💡 Responsibilities

Lead the development of clear and differentiated marketing strategies and actionable plans to support peri-launch and launched assets.
Challenge cross-matrix stakeholders to find opportunities and address challenges for assets.
Critically review competitor data and advancements to assess market threats, differentiation opportunities, and use cases.
Support key internal and external turning points by leading assessments and deliverables to accelerate launch readiness.
Collaborate with the Global Marketing Lead, Medical Affairs, and Commercial Insights leads to gather deep marketplace insights and develop a “gold standard” commercial strategy designed to optimize the future value of peri-launch assets.
Guide the Integrated Brand Team and global marketing activities, fostering global engagement with local market alignment.
Shape high-quality marketing deliverables aligned with Amgen’s processes and requirements, including contributions to Global Product Strategy, brand planning, launch readiness, competitive insights, patient-centric deliverables, robust Target Product Profiles, forecasts, and strategies to enhance program value and expand patient impact opportunities.
Partner with global markets to develop and implement launch tactics.
Generate end-to-end commercial plans for assets and drive activities across the IBT and markets.
Commission and manage market research in collaboration with Commercial Data & Analytics (cDNA).
Work with Competitive Intelligence to closely monitor the competitive landscape and its implications for Amgen’s strategy.
Partner with Forecasting and Finance to develop long-range sales and operating expense projections.
Lead the creation of aligned narratives for internal and external communications.
Ensure effective leverage of lead markets by ROW markets (e.g., promoting broad usage of existing materials to avoid duplication) using a central repository.
Coordinate and deliver best practice sharing in collaboration with lead and ROW markets.
Address questions and requests from other markets related to global strategy.
Assist in managing launch readiness activities and quarterly reviews.
Support alliance management and external relations when applicable.
Partner with priority country GMs to critically review, challenge, and update brand plans and long-range sales forecasts (LRS).
Oversee deliverables to ensure alignment with global assets and therapeutic area strategies.
Support Business Unit Director (BUD) forums and marketer interchange initiatives in collaboration with global sponsors.

LeadershipProject ManagementData AnalysisPeople ManagementCross-functional Team LeadershipProduct DevelopmentBusiness OperationsStrategic ManagementCommunication SkillsAnalytical SkillsCollaborationProblem SolvingNegotiationPresentation skillsRelationship buildingBudgetingSales experienceMarket ResearchMarketingTeam managementStakeholder managementStrategic thinkingFinancial analysisEnglish communication

Posted 25 days ago

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🔥 Medical Director, Global Medical Affairs Lead, Diabetes and Metabolism - US, Remote

Posted 30 days ago

📍 United States of America

💸 240754.0 - 277917.0 USD per year

🔍 Biotechnology

🔧 Requirements

Doctorate degree and 4 years’ experience in a leadership role in clinical research and/or medical affairs OR Master's degree and 8 years OR Bachelor's degree and 10 years.
At least 4 years’ managing experience.
Preferred: MD with fellowship in Endocrinology or related field.
Clinical experience in diabetes and metabolic conditions.
Experience in building Integrated Evidence Generation Plans.

💡 Responsibilities

Contribute to the development and execution of the global medical affairs strategy for Diabetes related products.
Serve as the Medical Affairs Representative on various global strategic teams.
Support integrated evidence generation plans and capture clinical insights.
Facilitate scientific engagements with KOLs and partners.
Align strategy for medical communications and ensure consistent execution.
Provide strategic direction for study design and access to medicines.

LeadershipCollaborationCompliance

Posted 30 days ago

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🔥 Director, R&D Process Quality Business Intelligence & Data Analytics

Posted 30 days ago

📍 United States, United Kingdom, Portugal

💸 187972.0 - 214012.0 USD per year

🔍 Pharmaceutical/Biotech

🔧 Requirements

Doctorate degree and 4 years of quality experience OR Master’s degree and 8 years of quality experience OR Bachelor’s degree and 10 years of quality experience
4 years experience directly managing people and leadership experience leading teams, projects, programs, or directing the allocation of resources.
15 years or more experience in Quality Management, Quality Assurance, Continuous Improvement, or other relevant areas of the pharmaceutical/biotech industry where risk-based quality management and quality by design are a core responsibility.
Oversight and implementation of Quality Management Systems and experience managing quality in electronic QMS such as Veeva or Trackwise.
Thorough understanding of Clinical R&D activities and Global Regulations.
Well versed in the development of quality measures including their creation and usage in a complex, cross-functional/matrixed environment.
Strong analytical capabilities - experience with process monitoring, including the application of advanced analytical methods and modern technology used to enable signal detection and quality improvement (e.g., Spotfire, PowerBI, Python).

💡 Responsibilities

Provide systematic and strategic methods to assess and measure Quality as a competitive advantage for Amgen R&D.
Provide strategic leadership in developing and implementing systematic methods to measure and improve R&D quality, ensuring alignment of all data analytics and business intelligence initiatives with broader organizational goals and evolving regulatory requirements.
Ensure People, Processes, Systems, Data Analytics and Innovation are used effectively to move Quality Culture towards a proactive predict and prevent culture.
Effectively lead, collaborate and partner with internal R&D team members to analyze and resolve issues and risks to drive clear scope, sponsorship, planning and execution.
Lead and support management directed data driven projects that are of large impact/scope and thus risk for Amgen clinical trials and pre-clinical research activities.
Support Amgen’s procedural framework through the development, maintenance, and communication of procedural performance measures/indicators; ensure that all procedures maintain compliance to relevant laws, regulations, and internal quality standards; so that Amgen treats all research subjects ethically and safely, and all data is generated with full integrity.
Ensure that all of Amgen’s research procedures are properly measured for performance and that key partners, including management, are informed regularly; work to support the management review system within the Amgen QMS through timely generation of reports and tracking of key actions.
Support the procedural change process through the communication of metrics designed in collaboration with the Business Process Owner network and leadership across R&D functional areas.
Collaborate with Business Process Owners and apply risk-based strategies consistently to identify and mitigate risks towards the continuous advancement of Amgen’s R&D QMS.
Lead the application of process metrics (KQI, KPI - leading and lagging) and modern analytic methods across the Business Process Network to support periodic review by management to ensure maintenance of QMS health.
Collaborate with other quality professionals within R&D to support the QMS continuous improvement cycle (Plan, Do, Check, Act), including Deviation Management/ Corrective and Preventative Actions (CAPA).

LeadershipProject ManagementPythonSQLBusiness IntelligenceData AnalysisPeople ManagementCross-functional Team LeadershipBusiness OperationsFinancial ManagementStrategic ManagementCommunication SkillsAnalytical SkillsCollaborationProblem SolvingAgile methodologiesWritten communicationComplianceMS OfficeTeamworkData entryQuality AssuranceRisk ManagementData visualizationProcess improvementData modelingData analyticsChange Management

Posted 30 days ago

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🔥 Commercial Programs Quality Oversight- Remote

Posted about 1 month ago

📍 United States of America

🧭 Full-Time

💸 158678.0 - 191613.0 USD per year

🔍 Biotechnology

🔧 Requirements

Doctorate degree and 3 years of R&D, Operations and/or Quality experience in the PhRMA/Biotech sector.
Master’s degree and 7 years of R&D, Operations and/or Quality experience in the PhRMA/Biotech sector.
Bachelor’s degree and 9 years of R&D, Operations and/or Quality experience in the PhRMA/Biotech sector.
Associate’s degree and 12 years of R&D, Operations and/or Quality experience in the PhRMA/Biotech sector.
High school diploma/GED and 14 years of R&D, Operations and/or Quality experience in the PhRMA/Biotech sector.
Minimum of 3 years experience directly managing people and/or leadership experience leading teams, projects, or programs.

💡 Responsibilities

Provide quality oversight for Patient Support Programs, Market Research, Digital Health, Websites, and Social Media.
Lead audits and monitoring visits for Amgen products.
Manage compliance issues and enhance proactive quality management processes.
Report significant compliance issues to R&D Quality management.
Serve as the PV representative on senior compliance/quality oversight bodies.

LeadershipProject ManagementComplianceMarket ResearchQuality AssuranceRisk ManagementStakeholder management

Posted about 1 month ago

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