Study Delivery Sr Associate
Amgen · Hyderabad, India
Clinical OperationsFull-timeCompany career page
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Role summary
This senior-level role supports clinical study teams in executing trials with accuracy and compliance. Responsibilities include managing study timelines, tracking enrollment and data quality, coordinating with sites and vendors, and escalating risks to stakeholders. The position offers exposure to multiple studies across their full lifecycle, located in Hyderabad.
What they're looking for
- Master's degree, or Bachelor's plus 2 years clinical execution experience
- 3 years life sciences/medical field experience with 1 year biopharmaceutical clinical research
- Proficiency in CTMS, eTMF, EDC, and Microsoft Office applications
- Strong clinical trial process expertise in biotech, pharma, or CRO settings
- Experience overseeing vendors, managing data flow, and executing risk-based monitoring
- Knowledge of regulatory compliance, CAPA processes, and inspection readiness protocols
What you'll be doing
- Develop and maintain study trackers, dashboards, timelines, and vendor management tools for visibility
- Monitor global enrollment, data quality, and key indicators; address deviations and escalate risks
- Coordinate study start-up activities including system setup, access management, and documentation
- Lead vendor setup, recruitment strategy delivery, and training system oversight
- Manage trial documentation systems and support audit/inspection readiness activities
Privacy & handoff
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