Observational Research Manager - Cardiovascular

Before you apply

Job source

Himalayas

Applying on

himalayas.app

Workplace

Fully remote

US state

Nationwide remote

Category

Project Management

Link last checked

Not checked yet

Posted

2 weeks ago

Closes

11/3/2026

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About the role

Job Title: Observational Research Manager - Cardiovascular Job Location: Washington D.C., District of Columbia, United States Job Location Type: Remote Job Contract Type: Full-time Job Seniority Level: HOW MIGHT YOU DEFY IMAGINATION? You’ve worked hard to become the professional you are today and are now ready to take the next step in your career. How will you put your skills, experience and passion to work toward your goals? 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, reaching over 10 million patients worldwide. Come do your best work alongside other innovative, driven professionals in this meaningful role. Observational Research Manager Live What you will do Let’s do this. Let’s change the world. In this vital role you will be working with multiple teams to generate real world evidence supporting a wide variety of business needs. The increasing demand for real-world evidence (RWE) from regulatory and reimbursement authorities makes observational research a key component of drug development and commercialization. Amgen's Center for Observational Research (CfOR) is a global organization with an industry-leading analytical capability that generates RWE to support business needs across a product’s lifecycle. CfOR scientists partner with internal team members and industry experts to design, conduct, interpret and publish observational research that informs decision-making from the early development of a molecule to the design of clinical trials and the safety and efficacy of Amgen medicines. CfOR studies include but are not limited to evidence generation regarding the frequency and distribution of disease, the clinical burden of disease, the natural history or clinical course of disease, the design of clinical trials, treatment cost and utilization patterns, and the safety and effectiveness of therapeutic interventions. In this role you will have responsibilities for research activities on product-facing teams in the therapeutic area of cardiovascular disease. A CfOR Manager is recognized as a strong scientific contributor and is a first or contributing author for papers in peer-reviewed journals, abstracts for scientific congresses or for internal reports that enhance the company’s mission. Key Activities include: Manage descriptive epidemiologic studies to characterize the incidence/prevalence of disease in US, EU, Asia, and emerging market countries Manage research projects involving the analysis of multiple types of data including medical claims, electronic health records, and prospective observational cohort studies Provide safety research support across the life cycle of Amgen products, supports the development of risk management plans, and implements pharmacovigilance studies Conduct literature reviews and prepares research reports and scientific manuscripts Stay abreast of the latest developments in the field of observational research and drug development Promote awareness, understanding, and use of observational research methods Communicate scientific information to a variety of audiences 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 Or Master's degree and 2 years of scientific experience Or Bachelor's Degree and 4 years of scientific experience Or Associate’s degree and 8 years of scientific experience Or High school diploma / GED & 10 years of scientific experience Preferred Qualifications: Doctorate in Epidemiology or other subject with high observational research content Experience in cardiovascular disease Experience in the design, execution, and analysis of observational research studies within Pharmaceutical or Public Health setting Experience in research to support drug development Experience working with secondary data systems, including administrative claims, E

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