Cardiovascular Observational Research Manager - Remote

BioSpace; Washington (District of Columbia); Hybrid; USD 140,000 - 190,000; Full time

Benefits offered by this job

Health and welfare plans

Retirement savings plan

Stock-based incentives

Flexible work models

Job summary

Amgen seeks an Observational Research Manager to advance real-world evidence across cardiovascular programs. You will lead descriptive epidemiologic studies, manage projects using claims, EMR, and registries, and publish findings to inform development and commercialization.

You will collaborate with CfOR scientists and cross-functional teams, contribute to study design, safety research, and risk management plans, and help translate real-world evidence into clinical impact.

Qualifications

• Doctorate in a scientific field or equivalent.
• Master's degree with 2 years of scientific experience.
• Bachelor's degree with 4 years of scientific experience.
• Associates degree with 8 years of scientific experience.
• High school diploma with 10 years of scientific experience.

Responsibilities

• Manage descriptive epidemiologic studies to characterize disease incidence/prevalence in US, EU, Asia, and emerging markets.
• Manage research projects analyzing medical claims, EMR, and cohort data.
• Provide safety research support across product lifecycles and pharmacovigilance studies.
• Conduct literature reviews and prepare research reports and manuscripts.
• Stay updated on observational research and drug development developments.
• Promote awareness and use of observational research methods.
• Communicate scientific information to diverse audiences.

Skills

Observational research

Biostatistics

Communication skills

Project management

Education

Doctorate degree

Master's degree

Bachelor's degree

Associates degree

High school diploma

Tools

Administrative claims data

Electronic health records (EMR)

Registries

Job description

Amgen seeks an Observational Research Manager to advance real-world evidence across cardiovascular programs. You will lead descriptive epidemiologic studies, manage projects using claims, EMR, and registries, and publish findings to inform development and commercialization.

You will collaborate with CfOR scientists and cross-functional teams, contribute to study design, safety research, and risk management plans, and help translate real-world evidence into clinical impact.