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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 supports global clinical trials by managing study logistics, data systems, and vendor coordination. The Senior Associate leads tracker and dashboard creation, oversees start‑up activities, monitors enrollment and quality metrics, and escalates risks with solutions. Works onsite in Hyderabad, collaborating with study managers, sites, and vendors to ensure compliant, on‑time study execution.

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 global enrollment, data flow, and quality indicators
  • Lead risk and quality management activities
  • Engage vendors and suppliers for study deliverables
  • Maintain clinical trial systems (CTMS, eTMF, EDC) and ensure data accuracy
  • Support audit/inspection readiness and CAPA processes

What you’ll bring

  • 2 years clinical execution experience (Bachelor)
  • 6 years clinical execution experience (Associate)
  • 8 years clinical execution experience (High school)

Nice to have

  • 3 years life sciences experience
  • 1 year biopharma clinical research

Skills

Study coordinationRisk managementVendor managementCTMSeTMFData monitoringRegulatory complianceProcess improvement

Education

  • Master's degree
  • Bachelor's degree
  • Associate's degree
  • High school diploma