Study Delivery Associate
Amgen · Hyderabad, India
Clinical OperationsFull-timeCompany career page
The apply link worked recently (not employer-confirmed).
Role summary
Study Delivery Associate provides administrative and operational support to clinical trial management at Amgen in Hyderabad. The role focuses on study coordination, data systems management, document preparation, and ensuring regulatory compliance across clinical trial activities.
What they're looking for
- Bachelor's degree, or Associate's degree with 4 years clinical execution experience
- 2 years life sciences or medically related work experience preferred
- 1 year biopharmaceutical clinical research experience in biotech, pharma, or CRO
- Proficiency with CTMS, eTMF, EDC, and Microsoft Office applications
- Knowledge of clinical trial processes, document tracking, and regulatory submissions
- Strong data entry accuracy and ability to manage clinical trial information flow
- Cultural sensitivity and ability to collaborate across global teams
What you'll be doing
- Maintain study-level trackers, dashboards, timelines, and communicate progress to Study Delivery Manager
- Track study actions and risk mitigation activities; prepare risk and quality review documentation
- Manage clinical trial system data entry and access requests for CTMS and training systems
- Prepare, review, and maintain study documentation including regulatory submissions and monitoring plans
- Support study start-up activities, biological sample management, and investigational product logistics
Privacy & handoff
This role links to Amgen's own application system. RoleLantern records your interest and checks the link, but the application happens on the employer's site and status updates may not come back to us. Clicking apply does not mark you as applied automatically.