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Join Amgen’s Mission of Serving Patients. At Amgen, if you feel like you’re part of something bigger, it’s because you are. Our shared mission—to serve patients living with serious illnesses—drives all that we do. Since 1980, we’ve helped pioneer the world of biotech in our fight against the world’s toughest diseases. With our focus on four therapeutic areas –Oncology, Inflammation, General Medicine, and Rare Disease– we reach millions of patients each year. As a member of the Amgen team, you’ll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives.
Job Responsibility:
Lead the acquisition, integration, and quality management of non-CRF (external/vendor) clinical trial data
Ensure timely, accurate, and fit-for-purpose data to support study delivery, analytics, with regulatory compliance
Own the design, setup, and ongoing management of non-CRF data
Own, define and maintain vendor data transfer specifications
Ensure timely and accurate ingestion of external datasets
Partner with other Data Management roles and study team to align external data with CRF structures
Lead troubleshooting of vendor integration issues
Monitor the quality of incoming data throughout the study lifecycle
Requirements:
Master’s degree and 8 years of clinical execution experience OR
Bachelor’s degree and 8 years of clinical execution experience OR
8 years’ work experience in life sciences or medically related field, including 3 years of biopharmaceutical clinical research experience obtained working on clinical trials in a biotech, pharmaceutical or CRO company
Experience engaging and working across clinical trial teams in multiple geographies to deliver global clinical trials
Experience in management and oversight of external vendors (e.g., CROs, central labs, imaging vendors, etc.)