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Hiring companyAmgen
Verified today
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 ensuring study execution is timely, high‑quality and compliant. The Senior Associate leads study planning, coordination and execution tasks such as tracker maintenance, vendor management, enrollment monitoring and risk mitigation. Works with Study Managers and cross‑functional teams to drive start‑up activities, data integrity and audit readiness. Hyderabad, on‑site role with occasional travel for site visits.
What you’ll do
- Lead development and maintenance of study trackers, dashboards and timelines
- Coordinate investigator meetings, trial events and site communications
- Manage start‑up activities such as system setup and document readiness
- Monitor enrollment, data flow and quality indicators, addressing deviations
- Deliver risk and quality management activities and support audit readiness
- Maintain clinical trial systems (CTMS, eTMF) and ensure accurate data entry
- Engage vendors and suppliers to ensure consistent deliverables
- Build relationships with internal teams, vendors and investigator sites
What you’ll bring
- Master’s degree or Bachelor’s with 2 years clinical execution experience
- Associate’s degree with 6 years experience
- High school diploma/GED with 8 years experience
Nice to have
- 3 years life‑sciences experience, including 1 year biopharma clinical research
- Experience on global clinical trials
Skills
Study planningRisk managementVendor managementCTMSeTMFData monitoringRegulatory complianceProcess improvement
Education
Bachelor's