Amgen is a global biotechnology leader focused on discovering, developing, and delivering innovative medicines. With over 40 years of scientific excellence, Amgen continues to advance healthcare using cutting-edge biology and technology.
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📌 Job Overview
- Role: Study Delivery Senior Associate
- Location: Hyderabad
- Job Type: Full-Time
- Department: Clinical Research / Study Delivery
- Job ID: R-232826
- Experience Level: Mid-Level
🚀 Why This Role Matters
This Study Delivery Senior Associate job in Hyderabad is a critical role in global clinical trials. You’ll support study execution, ensure compliance, and collaborate with cross-functional teams—making it an excellent opportunity for professionals seeking growth in clinical research jobs in India.
🧪 Key Responsibilities
🔹 Study Planning & Coordination
- Develop and manage study trackers, dashboards, and timelines
- Coordinate investigator meetings and clinical trial logistics
- Support study start-up activities and documentation readiness
🔹 Study Execution & Oversight
- Monitor enrollment, data quality, and trial performance
- Manage risk and quality activities in clinical trials
- Track study progress and resolve operational issues
🔹 Stakeholder & Vendor Management
- Collaborate with global teams, vendors, and sites
- Act as a communication point for study updates
- Support vendor setup and performance monitoring
🔹 Data & Compliance Management
- Maintain systems like CTMS, eTMF, and EDC
- Ensure accurate clinical data entry and reporting
- Manage trial documentation for audit readiness
🔹 Process Improvement
- Contribute to process optimization and automation
- Support audits, inspections, and CAPA implementation
🎓 Qualifications
✅ Basic Qualifications
- Master’s degree OR
- Bachelor’s degree + 2 years clinical research experience OR
- Diploma/Associate degree + relevant experience
✅ Preferred Qualifications
- 1–3 years in clinical trials / CRO / pharma industry
- Experience in global clinical trials
- Knowledge of CTMS, eTMF, EDC systems
🎯 Eligible Degrees
- B.Pharm / M.Pharm / Pharm.D
- B.Sc / M.Sc (Life Sciences, Clinical Research)
💡 Required Skills
- Strong communication & collaboration
- Clinical trial operations knowledge
- Risk management & compliance expertise
- MS Office & clinical systems proficiency
- Documentation and regulatory understanding
🎁 Benefits & Perks
- Opportunity to work with a global biotech leader
- Exposure to international clinical trials
- Career growth in clinical research domain
- Collaborative and innovative work environment
- Competitive salary and benefits package
📥 How to Apply
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