Study Delivery Sr Associate
Amgen · Hyderabad, India
Clinical OperationsFull-timeCompany career page
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Role summary
Amgen seeks a Study Delivery Senior Associate to provide clinical study management support in Hyderabad, ensuring compliant and timely execution of global trials. The role involves coordinating study logistics, monitoring enrollment and data quality, managing vendor relationships, and escalating risks to support operational excellence.
What they're looking for
- Master's degree, or Bachelor's with 2+ years clinical execution experience
- 3 years life sciences or medical field experience with 1+ year biopharmaceutical clinical research
- Proficiency in CTMS, eTMF, EDC systems and Microsoft Office suite
- Experience overseeing vendors and executing risk-based site monitoring
- Strong documentation accuracy, data management, and regulatory compliance skills
- Knowledge of clinical trial processes in biotech, pharmaceutical, or CRO environments
What you'll be doing
- Develop and maintain study trackers, dashboards, timelines, and vendor management tools
- Monitor global enrollment, data flow, and quality metrics using dashboards and reports
- Coordinate study start-up activities including system setup and document readiness
- Lead risk and quality management activities and escalate deviations with proposed solutions
- Manage clinical trial data systems, documentation, and support audit and inspection readiness
Privacy & handoff
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