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Study Delivery Sr Associate
About the role
Amgen’s Study Delivery team in Hyderabad ensures clinical trials run smoothly by managing study timelines, regulatory compliance, and data integrity. The Sr Associate coordinates study trackers, system access, and vendor logistics while maintaining CTMS and eTMF data. This role supports global site communications, risk reviews, and TMF filing, contributing to process improvement and knowledge sharing across the organization.
What you’ll do
- Maintain study trackers and dashboards
- Communicate progress to Study Delivery Manager
- Track and follow up on study actions and risk mitigation
- Prepare and file regulatory documents
- Support system access and vendor relationships
- Coordinate investigational product logistics
- Ensure data entry accuracy in CTMS
What you’ll bring
- Bachelor’s degree
- 4+ years clinical execution experience
- Proficiency in CTMS, eTMF, MS Office