Study Delivery Associate in Hyderabad, India - Jobeax
Vacancy description
Study Delivery Associate in Hyderabad, भारत
Amgen
Hyderabad, भारत
The Study Delivery Associate supports clinical trial management by coordinating study activities, maintaining regulatory compliance, and managing clinical systems and documentation. Based in Hyderabad, India, this role ensures accurate data entry, tracks study progress, and facilitates communication across the study team and investigator sites.
Responsibilities
Establish and maintain study trackers, dashboards, and timelines for clinical trials
Enter and verify accurate, timely data in clinical trial management systems
Prepare, review, and organize regulatory documentation including protocols and informed consent forms
Coordinate study startup activities, site communications, and investigator meeting logistics
Track study actions, risk mitigation efforts, and training completion for regulatory readiness
Requirements
Bachelor's degree, or Associate's degree with 4 years clinical execution experience
2 years life sciences or medical field experience, including 1 year biopharmaceutical clinical research
Proficiency with CTMS, eTMF, EDC, and Microsoft Office applications
Knowledge of clinical trial processes, regulatory requirements, and document management standards
Strong data entry accuracy and ability to manage clinical trial information systems
Cultural sensitivity and ability to collaborate with global teams
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 ...
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