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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 about 1 year agoBiotechnology Research

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🔥 IS Senior Manager, MyAmgen Product Owner - US Remote - East Coast

Posted 1 day ago

📍 United States

🧭 Full-Time

💸 140490.0 - 169210.0 USD per year

🔍 Biotechnology

Doctorate, Master's, Bachelor's, Associate’s, or High school diploma with varying years of experience in managing Finance Data Model.
Ability to define and drive a product vision and roadmap.
Strong collaboration and communication skills.
Proficiency in handling product budgets.
Solid technical background to guide development efforts effectively.

Define, maintain, and drive the strategic roadmap for the MyAmgen platform.
Collaborate closely with business partners to meet their needs and deliver measurable value.
Manage the MyAmgen product team, including developers, analysts, and vendors.
Champion the product vision in alignment with strategy and employee needs.
Oversee the product budget and governance processes.

PythonSQLAgileSalesforceCross-functional collaborationData modelingBudget management

Posted 1 day ago

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🔥 Sr. Manager, Consumer Marketing, Rare Disease (Remote)

Posted 3 days ago

📍 United States of America

💸 152128.0 - 179472.0 USD per year

🔍 Biotechnology

Basic Qualifications: Doctorate degree and 2 years of digital marketing experience OR Master’s degree and 4 years, OR Bachelor’s degree and 6 years, OR Associate’s degree and 10 years, OR High school diploma/GED and 12 years of experience.
Preferred Qualifications: Prior marketing and/or agency experience in healthcare; relevant experience managing digital media channels.
Knowledge of data analysis to drive recommendations; understanding of pharmaceutical regulatory requirements.
Strong project management skills and ability to work in a fast-paced environment.
Excellent written and verbal communication skills.

Develop an understanding of Thyroid Eye Disease (TED) and characteristics of TED patients.
Own the ongoing development of consumer digital strategy and tactics.
Define, track, measure, and report on all digital KPIs using analytics to optimize programs.
Manage branded and unbranded social content and programmatic display advertising.
Manage internal and external agencies to meet project objectives and budgets.
Collaborate with cross-functional business partners and ensure compliance with regulations.

Project ManagementData AnalysisDigital Marketing

Posted 3 days ago

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🔥 Safety and Medical Quality Lead - Observational Research

Posted 4 days ago

📍 United Kingdom

🔍 Biotechnology

Degree Educated.
Proven experience in R&D, Operations, and/or Quality in the Pharma/Biotech sector.
Demonstrated leadership expertise in developing teams and coordinating projects.
Proven track record with auditing, preferably in GPvP or GCP.
Good knowledge of global regulatory requirements for GPvP/GCP.

Plan, conduct and report on risk-based GPvP audits.
Assess and manage risks, including developing the annual GPvP audit plan.
Provide quality input for risk assessment related to Observational research studies.
Act as Quality Lead contact for vendor evaluation and oversight in Observational research.
Support inspections and external audits, and improve R&D processes with CAPA.

Quality AssuranceRisk Management

Posted 4 days ago

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🔥 Case Manager - Rare Disease- TEPEZZA - US Remote

Posted 4 days ago

📍 United States of America

💸 87151.0 - 98921.0 USD per year

🔍 Biotechnology

Master’s degree or Bachelor’s degree and 2 years of Case Management experience.
Associate’s degree and 6 years of Case Management experience or High school diploma with 8 years of Case Management experience.
5+ years of experience in the pharmaceutical industry preferred.
2+ years prior experience as a Case Manager.
Excellent communication skills and commitment to customer service.
Ability to resolve hurdles across multiple cases simultaneously.
Familiarity with HIPAA and FDA regulations.
Proficiency in Excel and PowerPoint.
Up to 20% travel required.

Experience day to day oversight of patient customer service issues with insurance.
Daily interaction with Regional Business Managers, Patient Access Liaison, and Medical Science Liaison to ensure accurate communication on insurance status.
Manage all steps required to gain access to therapy in collaboration with RBMs and pharmacies.
Report adverse events and maintain case history for all U.S. patients.
Track reimbursement and shipping status and resolve reimbursement issues.
Liaise with medical offices for insurance authorizations and counsel patients on insurance options.
Identify adherence trends and manage Open Enrollment efforts.

Communication SkillsCustomer serviceProblem-solving skillsData entryRelationship managementPowerPoint

Posted 4 days ago

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🔥 EH&S Manager

Posted 7 days ago

📍 United States of America

🧭 Full-Time

💸 103769.0 - 130498.0 USD per year

🔍 Biotechnology

High school diploma/GED and 10 years of EH&S experience; or Associate’s degree and 8 years of experience; or Bachelor's degree and 4 years of experience; or Master's degree and 2 years of experience; or Doctorate.
5-10 years in the pharmaceutical/biotech industry preferred.
Experience leading biological safety and industrial hygiene programs.
Proficient in risk assessments and sampling strategies.
Skilled in program development and project management.
Experience with regulatory agencies and inspections.
Current qualification as a Hazardous Material Technician under Federal HAZWOPER.
Professional qualifications preferred, such as CSP, CIH, RBP, or CBSP.

Lead safety and health programs at the Thousand Oaks location.
Ensure compliance and continuous improvement of site safety programs including Industrial Hygiene.
Provide strategic leadership and expert advice on chemical exposure evaluations.
Function as the site Biological Safety Officer.
Support Research and Development, Product Development, and clinical manufacturing staff.
Implement best practices with internal clients to ensure compliance.
Coach and mentor EH&S industrial hygiene staff.
Create processes to ensure compliance with environmental health and safety regulations.
Review safety records for completeness and compliance.
Facilitate training and prepare regulatory reports.
Interface with regulatory agencies during inspections.
Promote safety culture and assess EH&S impacts.
Identify program improvement opportunities through data analytics.

LeadershipProject ManagementData AnalysisComplianceRisk Management

Posted 7 days ago

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🔥 Clinical Research Medical Director - Obesity/Cardiovascular, US - Remote

Posted 7 days ago

📍 United States

🧭 Full-Time

💸 256334.0 - 318868.0 USD per year

🔍 Biotechnology

MD or DO degree from an accredited medical school.
2 years of clinical research experience and/or basic science research.
Preferred: 3 years of clinical research in biopharmaceutical industry.
5 years of combined clinical research experience, teaching, and patient care activities.
Strong clinical development experience in endocrinology or cardiology.
Knowledge of product development and commercialization processes.
Experience in developing clinical trial designs and study concepts.
Knowledge of Good Clinical Practices (GCP) and applicable regulations.
Demonstrated leadership potential in a complex matrix environment.
Strong interpersonal and problem-solving skills.

Play a leadership role in obesity studies related to AMG 133.
Provide clinical/scientific knowledge for the global evidence generation plan.
Support collaborations with cross-functional medical and commercial teams.
Participate in safety and regulatory interactions.
Interpret clinical trial data and author study reports.
Develop KOLs and make presentations at scientific meetings.
Provide clinical content input for Scientific Affairs and the Commercial Organization.
Contribute to product profile and safety development.
Create development options for review committees.
Interact with various centers to innovate later development options.

LeadershipCross-functional collaboration

Posted 7 days ago

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🔥 Clinical Research Medical Director - Obesity/MASH, US - Remote

Posted about 2 months ago

📍 United States

💸 256334 - 318868 USD per year

🔍 Biotechnology

Doctorate degree and 2 years of experience in obesity, diabetes, MASH or metabolic diseases.
Accredited residency/fellowship in hepatology or endocrinology, board certified or equivalent.
2 years of clinical research experience and/or basic science research with clinical teaching.
Understanding of the scientific method and clinical applications.
Familiarity with clinical research concepts and trial design.
Ability to present complex medical concepts effectively in written and oral communication.

Support cross-functional and global collaborations to integrate medical and commercial input into development programs.
Participate in safety and regulatory interactions, providing clinical input during trials.
Author and QC study-related documents and review safety narratives.
Initiate database analyses for commercial/clinical objectives.
Contribute to clinical study reports and regulatory submissions.
Engage with regulatory agencies and develop key opinion leaders.

LeadershipData AnalysisPeople ManagementCross-functional Team LeadershipCommunication SkillsAnalytical SkillsCollaborationProblem SolvingAttention to detailOrganizational skillsPresentation skillsTime ManagementWritten communication

Posted about 2 months ago

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🔥 Clinical Research Medical Director, Endocrinology/Sleep Apnea, US - Remote

Posted about 2 months ago

📍 United States of America

🧭 Full-Time

💸 256334 - 318868 USD per year

🔍 Biotechnology

MD or DO degree from an accredited medical school.
2 years of clinical research experience and/or basic science research.
Five years of clinical research experience in biopharmaceutical industry focused on obesity or sleep-related disorders preferred.
Knowledge of pharmaceutical product development and commercialization processes.
Strong understanding of Good Clinical Practices (GCP) and regulatory guidelines.
Leadership experience in a complex matrix environment.

Provide clinical/scientific knowledge into the development and design of global evidence generation plans.
Support global collaborations to integrate medical and commercial input.
Provide clinical input for safety and regulatory interactions.
Oversee clinical study reports, publications, and regulatory submissions.
Develop relationships with key opinion leaders and present at scientific meetings.
Contribute to target product profile development and global product safety.
Interact with various teams to develop innovative later development options.

LeadershipData AnalysisPeople ManagementCross-functional Team LeadershipCommunication SkillsAnalytical SkillsCollaborationProblem SolvingAttention to detailPresentation skillsWritten communication

Posted about 2 months ago

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🔥 Biostatistical Programming Senior Manager- US Remote

Posted about 2 months ago

📍 United States

🧭 Full-Time

💸 154453 - 177836 USD per year

🔍 Biotechnology

Doctorate degree and 2 years, Master’s and 6 years, Bachelor’s and 8 years, Associate’s and 10 years, or High school diploma and 12 years of statistical programming experience in the Pharmaceutical industry.
Preferred skills include SAS Graph, SAS STAT, SAS Macro, SQL, and familiarity with R Programming language.
Experience in regulatory submissions and software development.
Ability to manage complex programming tasks and lead teams.

Accountable for Global Statistical Programming study deliverables and submission activities for Amgen products.
Set and drive programming strategies globally.
Plan and monitor project progress, addressing issues as necessary.
Support FSP relationship and ensure product goals are met.
Monitor and utilize assigned staff effectively.
Lead departmental process improvement initiatives.
Assist in audits and inspections.
Develop and implement global policies and SOPs.
Provide hands-on support and mentoring.

LeadershipProject ManagementSoftware DevelopmentSQLCommunication SkillsMentoringWritten communicationComplianceCoaching

Posted about 2 months ago

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