Study Delivery Associate
Amgen · Hyderabad, India
Clinical OperationsFull-timeCompany career page
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Role summary
Amgen seeks a Study Delivery Associate to support clinical trial operations in Hyderabad. The role involves coordinating study activities, managing trial data and systems, preparing documentation, and ensuring regulatory compliance across clinical research projects.
What they're looking for
- Bachelor's degree, or Associate's degree with 4 years clinical execution experience, or high school diploma with 6 years clinical execution experience
- Proficiency with CTMS, eTMF, EDC systems and Microsoft Office applications
- Knowledge of clinical trial processes, document management, and regulatory compliance requirements
- Experience tracking and filing essential trial documents including protocols and informed consent forms
- Preferred: 2 years life sciences experience with 1 year biopharmaceutical clinical research background
- Ability to work collaboratively across global teams with cultural sensitivity
What you'll be doing
- Support setup and maintenance of study trackers, dashboards, timelines and risk/quality reviews
- Maintain accurate data entry in clinical systems and manage study training and system access requests
- Coordinate study startup activities, site communications, investigator meetings, and biological sample logistics
- Prepare, review and file study documentation including regulatory submissions and trial master files
- Track study actions and deliverables, communicate progress to management, and support process improvements
Privacy & handoff
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