About this role
About the Role Amgen seeks a Sr Data Management Support to ensure high-quality clinical trial data across the study lifecycle by executing core data management activities, maintaining data integrity and compliance, and enabling timely study execution. What You'll Do
- Execute study data management tasks including database build testing, data cleaning, query management, reconciliation, and lock preparation with limited oversight
- Support core Data Management roles by owning time-sensitive deliverables with high-quality execution
- Actively contribute to setup and maintenance of EDC/non CRF data structures including local labs, coding dictionaries, along with non-CRF data integrations
- Track progress against data management timelines, study timelines and deliverables, identify risks or delays, and escalate issues with clear documentation and any mitigations
- Coordinate with local internal teams, global team members as well as external partners (including FSPs) when required to ensure aligned and efficient delivery of all study activities
- Identify opportunities to improve repeatable processes and contribute to best practices and knowledge sharing across the team What We're Looking For
- Basic Qualifications: Bachelor’s degree with 6 years of clinical execution experience
- Preferred Qualifications: 3 years’ work experience in life sciences or medically related field, including 1 year of biopharmaceutical clinical research experience obtained working on clinical trials in a biotech, pharmaceutical or CRO company