Job Information
Amgen Observational Research Senior Manager in Washington D.C., District Of Columbia
HOW MIGHT YOU DEFY IMAGINATION?
If you feel like you’re part of something bigger, it’s because you are. At Amgen, our shared mission—to serve patients—drives all that we do. It is key to our becoming one of the world’s leading biotechnology companies. We are global collaborators who achieve together—researching, manufacturing, and delivering ever-better products that reach over 10 million patients worldwide. It’s time for a career you can be proud of.
Observational Research Senior Manager
Live
What you will do
Let’s do this. Let’s change the world. Are you searching for a new, dynamic opportunity working with multiple teams to generate real world evidence supporting a wide variety of business needs? If so, we invite you to explore Amgen’s Center for Observational Research.
With a constantly growing demand for information from regulatory and reimbursement agencies, Observational Research (OR) is a critical component in drug development and commercialization. Amgen’s Center for Observational Research (CfOR) partners with internal and external teams to generate real world evidence for multiple partners across the entire product lifecycle. We generate evidence to inform the frequency, distribution, clinical burden, natural history, and clinical course of disease, the design of clinical trials, health resource utilization, drug utilization patterns, and the safety and effectiveness of our medicines.
In this vital role the Observational Research Senior Manager will be a member of the Bone team within CfOR and will be responsible for gathering insights and building collaborations and capabilities to advance the generation, use, and dissemination of real-world evidence (RWE) related to disease state epidemiology, treatment patterns, and medication safety and effectiveness to inform regulatory decision making and enhance access and use of Amgen’s medicines.
Responsibilities:
Lead the design, generation and delivery of RWE evaluating the safety and effectiveness of medicines to inform regulatory decision making (e.g., label expansion/change) and fulfill regulatory requirements across the globe.
Collaborate in the integrated evidence generation plan to align the conceptualization and design of RWE studies to the strategies and priorities of cross-functional partners.
Negotiate with cross-functional partners and enhance the use of RWE that can substitute for and/or complement interventional studies to reduce the time and cost of drug development and answer key business questions.
Facilitate the dissemination of RWE through publications, congress presentations, trainings, and development of scientific/promotional resources targeting a broad base of external partners (e.g., health care providers, payers, integrated delivery networks).
Contribute to the development and implementation of innovative analytic methods, and leverage CfOR’s internal data and analytics capabilities and tools to enable rapid, scalable and reproducible RWE.
Build external partnerships that can provide access to databases that can improve the quality and availability of real-world data in different patient populations and countries and facilitate execution of methodologically rigorous studies.
Contribute to CfOR’s mission in progressing innovative epidemiological methods and analytical capabilities to support CfOR’s leadership role within Amgen and across industry.
Win
What we expect of you
We are all different, yet we all use our unique contributions to serve patients. The professional we seek has these qualifications.
Basic Qualifications:
Doctorate degree and 2 years of related research and scientific experience
Or
Master's degree and 4 years of related research and scientific experience
Or
Bachelor's degree and 6 years of related research and scientific experience
Or
Bachelor's degree and 10 years of related research and scientific experience
Or
High School diploma / GED and 12 years of related research and scientific experience
Preferred Qualifications:
Doctorate in Epidemiology or other subject with high observational research content.
Experience in the design, execution and analysis of observation research studies within Pharmaceutical and/or Public Health settings.
Experience in research to support drug development.
Experience working with secondary data systems including administrative claims, EMR and registries.
Experience in observational research project planning and management.
Excellent communication, presentation and interpersonal skills.
Experience working with and leading multi-disciplinary teams.
Thrive
What you can expect of us
As we work to develop treatments that take care of others, we also work to care for our teammates’ professional and personal growth and well-being.
The expected annual salary range for this role in the U.S. (excluding Puerto Rico) is posted. Actual salary will vary based on several factors including but not limited to, relevant skills, experience, and qualifications.
Amgen offers a Total Rewards Plan comprising health and welfare plans for staff and eligible dependents, financial plans with opportunities to save towards retirement or other goals, work/life balance, and career development opportunities including:
Comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts.
A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan
Stock-based long-term incentives
Award-winning time-off plans and bi-annual company-wide shutdowns
Flexible work models, including remote work arrangements, where possible
Apply now
for a career that defies imagination
Objects in your future are closer than they appear. Join us.
careers.amgen.com
Application deadline
Amgen does not have an application deadline for this position; we will continue accepting applications until we receive a sufficient number or select a candidate for the position.
Amgen is an Equal Opportunity employer and will consider you without regard to your race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status.
We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.