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Hiring companyAmgen

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Study Delivery Senior Associate

Hyderabad,IN,India Full-time On-site

About the role

Clinical Study Delivery team at Amgen ensures global clinical trials run smoothly and compliantly. The Senior Associate supports study managers by maintaining trackers, coordinating logistics, managing start‑up activities, monitoring enrollment and data quality, and handling vendor and site engagements. Hyderabad office, on-site work model, with opportunities to work on global studies and contribute to process improvements.

What you’ll do

  • Develop and maintain study trackers, dashboards, and timelines
  • Coordinate investigator meetings, trial events, and site communications
  • Manage start‑up activities including system setup and document readiness
  • Monitor enrollment, data flow, and quality indicators, addressing deviations
  • Lead risk and quality management activities and escalation
  • Oversee vendor and supplier set‑up and performance
  • Maintain clinical trial systems and ensure accurate data entry
  • Contribute to process improvement and knowledge sharing

What you’ll bring

  • Master’s degree
  • Bachelor’s degree with 2 years clinical execution experience
  • Associate’s degree with 6 years clinical execution experience
  • High school diploma/GED with 8 years clinical execution experience

Nice to have

  • 3 years life sciences experience
  • 1 year biopharmaceutical clinical research experience
  • Experience with global clinical trials
  • Proficiency in MS Office, CTMS, eTMF, EDC

Skills

Study coordinationRisk managementVendor managementCTMSeTMFData monitoringProcess improvementRegulatory compliance

Benefits

  • Health insurance
  • Retirement savings plan
  • Paid time off
  • Employee assistance program

Education

Bachelor’s degree