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Hiring companyAmgen
Verified today
Study Delivery Senior Associate
Hyderabad,IN,India Full-time On-site
About the role
Study Delivery team at Amgen supports global clinical studies by ensuring timely, high-quality execution and compliance. The Senior Associate leads study planning, coordination, and execution tasks such as tracker maintenance, risk monitoring, vendor oversight, and data system management. Works with Study Managers and cross‑functional teams to drive enrollment, quality, and documentation readiness in Hyderabad, on‑site.
What you’ll do
- Develop and maintain study trackers, dashboards, and timelines
- Coordinate investigator meetings, trial events, and site communications
- Manage start‑up activities, system setup, and document readiness
- Monitor enrollment, data flow, and quality indicators, addressing deviations
- Lead risk and quality management activities and escalation
- Oversee vendor set‑up and ensure consistent deliverables
- 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, including 1 year biopharma clinical research
- Experience on global clinical trials
- Proficiency with MS Office, CTMS, eTMF, and EDC systems
- Vendor and supplier management experience
- Risk‑based monitoring and CAPA implementation
Skills
Clinical trial managementVendor oversightData monitoringRisk managementDocumentation complianceCTMSeTMFProcess improvement
Benefits
- Health insurance
- Retirement savings plan
- Paid time off
- Employee assistance program
Education
- Bachelor’s degree
- Master’s degree
- Associate’s degree
- High school diploma