Study Delivery Associate in Hyderabad, भारत

Amgen seeks a Study Delivery Associate to provide administrative and operational support for clinical trial management in Hyderabad. The role focuses on study coordination, data systems management, document preparation, and process improvement while ensuring regulatory compliance and study timelines are met.

Responsibilities

• Establish and maintain study-level trackers, dashboards, timelines, and risk mitigation documentation
• Enter and manage accurate data in clinical trial management systems and ensure system access compliance
• Prepare, review, and file regulatory documents including protocols, informed consent forms, and study guides
• Support study startup activities, training completion, site communications, and investigator meeting logistics
• Coordinate investigational product and biological sample logistics with reconciliation and compliance tracking

Requirements

• Bachelor's degree, or Associate's degree with 4 years clinical execution experience
• Proficiency in MS Word, Excel, PowerPoint, and clinical trial management systems
• Knowledge of CTMS, eTMF, EDC systems and document management practices
• Experience with clinical trial processes in biotech, pharmaceutical, or CRO settings
• Strong data entry, organizational, and regulatory compliance skills
• Ability to collaborate across global teams and manage multiple concurrent tasks