Job Overview
Location
United States - Remote
Job Type
Full-time
Category
Data Science
Date Posted
May 27, 2026
Full Job Description
đź“‹ Description
- • Support the design, start-up, and execution of global cardiovascular trials, ensuring adherence to protocol, regulatory requirements, and data integrity standards.
- • Contribute to the development of clinical protocols, statistical analysis plans, investigator brochures, and regulatory documents with focus on cardiovascular endpoints and safety outcomes.
- • Collaborate with cross-functional teams to support endpoint strategy, event adjudication processes, and cardiovascular safety monitoring.
- • Participate in the development and oversight of endpoint adjudication charters, safety monitoring plans, and interactions with Data Monitoring Committees (DMCs).
- • Provide clinical input into data management plans, CRF design, and clinical data review, with emphasis on cardiovascular outcomes endpoints (e.g., MACE, hospitalization events, mortality) and cardiac imaging endpoints.
- • Conduct ongoing clinical data review and signal detection to identify and resolve safety and data quality issues across global trial sites.
- • Support preparation and interpretation of interim analyses, database lock activities, and top-line data readouts.
- • Assist the Development Lead and Clinical Scientist Director with medical monitoring activities and oversight of CROs, vendors, and adjudication committees.
- • Collaborate with clinical operations, biostatistics, safety, regulatory, and medical affairs teams to ensure successful delivery of cardiovascular outcomes and/or cardiac imaging studies.
- • Contribute to clinical study reports, regulatory submissions, scientific publications, and presentations for internal and external stakeholders.
- • Identify operational or scientific risks and proactively implement mitigation strategies across cross-functional teams.
- • Apply working knowledge of study data readout activities including data cleaning, database lock, data extraction, endpoint validation, and generation of analysis outputs to support topline and final results.
- • Contribute to regulatory submission documents and support clinical regulatory responses for health authority interactions under guidance.
- • Serve as a contributing author on scientific publications or data presentations for internal forums or scientific conferences.
- • Utilize clinical data review and analysis tools such as Spotfire, listings review platforms, or other data visualization and analysis tools.
🎯 Requirements
- • Doctorate degree and 3 years of clinical development experience OR Master’s degree and 5 years of clinical development experience OR Bachelor’s degree and 7 years of clinical development experience OR Associate’s degree and 12 years of clinical development experience OR High school diploma / GED and 14 years of clinical development experience
- • 3 years of pharmaceutical clinical drug development experience, including experience supporting late-stage, global clinical trials
- • Industry or academic experience in cardiovascular medicine and/or cardiovascular outcomes trials; experience in large event-driven studies preferred
🏖️ Benefits
- • Comprehensive employee benefits package including Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts
- • Discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan
- • Stock-based long-term incentives
- • Award-winning time-off plans
- • Flexible work models where possible
Skills & Technologies
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About Amgen Inc.
Amgen Inc. is a global biotechnology company headquartered in Thousand Oaks, California. Founded in 1980, it discovers, develops, manufactures, and delivers human therapeutics targeting cancer, kidney disease, rheumatoid arthritis, bone disease, and other serious illnesses. Using advanced recombinant DNA and molecular biology techniques, Amgen produces biologic medicines such as Neulasta, Enbrel, and Prolia. The company operates R&D, manufacturing, and distribution facilities worldwide, investing heavily in genomic research to identify novel drug targets. Amgen also partners with academic institutions and smaller biotechs to expand its pipeline, aiming to transform breakthrough science into therapies that significantly improve patients’ lives.
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