Senior Manager, Oncology Real-World Evidence

Initial Therapeutics, Inc.; Washington (District of Columbia); Hybrid; USD 180,000 - 240,000; Full time

Job summary

Amgen is seeking an Observational Research Senior Manager in Oncology to lead projects across real-world evidence generation, study design, and dissemination. You will collaborate with scientific and commercial teams to advance observational research across the drug development and commercialization lifecycle.

Your role includes guiding study designs, building partnerships, and delivering high-quality RWE to support regulatory decisions and strategic initiatives.

Qualifications

• Doctorate or equivalent with related research experience.
• Experience in oncology observational research is preferred.
• Excellent communication and interpersonal skills.
• Experience leading multi-disciplinary teams.
• Research experience with secondary data systems (claims, EHR, registries).
• Strong project planning and study management.

Responsibilities

• Lead projects and teams to generate high-quality real-world evidence.
• Develop study proposals using real-world data to address key business questions.
• Design, complete, and deliver observational research studies.
• Disseminate RWE through publications, presentations and trainings.
• Collaborate on integrated evidence generation plans for product teams.
• Develop innovative analytic methods using internal data to inform decisions.
• Partner with collaborators to expand data sources and improve data quality.

Skills

Observational research

RWE methodology

Cross-functional leadership

Scientific communication

Critical thinking

Team leadership

Education

PhD in epidemiology or related

Master's in data science

Bachelor's in data sciences

Job description

Amgen is seeking an Observational Research Senior Manager in Oncology to lead projects across real-world evidence generation, study design, and dissemination. You will collaborate with scientific and commercial teams to advance observational research across the drug development and commercialization lifecycle.

Your role includes guiding study designs, building partnerships, and delivering high-quality RWE to support regulatory decisions and strategic initiatives.