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Hiring companyAmgen

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Study Delivery Sr Associate

Hyderabad,India Full-time On-site

About the role

Amgen’s Study Delivery team in Hyderabad ensures clinical trials run smoothly by managing study timelines, regulatory compliance, and data integrity. The Sr Associate coordinates study trackers, system access, and vendor logistics while maintaining CTMS and eTMF data. This role supports global site communications, risk reviews, and TMF filing, contributing to process improvement and knowledge sharing across the organization.

What you’ll do

  • Maintain study trackers and dashboards
  • Communicate progress to Study Delivery Manager
  • Track and follow up on study actions and risk mitigation
  • Prepare and file regulatory documents
  • Support system access and vendor relationships
  • Coordinate investigational product logistics
  • Ensure data entry accuracy in CTMS

What you’ll bring

  • Bachelor’s degree
  • 4+ years clinical execution experience
  • Proficiency in CTMS, eTMF, MS Office

Skills

CTMSeTMFMS OfficeData ManagementRisk ManagementVendor CoordinationProcess ImprovementDocumentation