Study Delivery Associate in 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