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Hiring Study Delivery Senior Associate (TMF / Clinical Research)
Amgen is hiring Study Delivery Senior Associate professionals for clinical trial operations, TMF management, CTMS support, and study coordination activities in Hyderabad.
This opportunity is ideal for candidates with 1–3 years experience in Clinical Research, CROs, Study Delivery, TMF, or Clinical Operations.
👉 Learn Clinical Research Career Path: Clinical Research Career Guide
📘 Learn Clinical Data & TMF Concepts: Clinical Data vs Clinical SAS
🏢 About Amgen
Amgen is a leading global biotechnology company focused on discovering, developing, and delivering innovative medicines for serious illnesses. With over 40 years of scientific innovation, Amgen works across oncology, cardiovascular diseases, inflammation, and rare diseases.
- Global biotechnology leader
- Advanced clinical research ecosystem
- Strong innovation & compliance culture
- Worldwide clinical development operations
📋 Job Overview
- Role: Study Delivery Senior Associate
- Company: Amgen
- Location: Hyderabad
- Department: Clinical Research / Study Delivery
- Experience: 1–3 Years
- Employment Type: Full-Time
- Job ID: R-232826
- Salary: ₹5.5 – ₹10 LPA (Estimated)
📌 Key Responsibilities
🧪 Study Planning & Coordination
- Develop study trackers & dashboards
- Coordinate investigator meetings
- Support clinical study startup activities
- Manage study timelines & milestones
📊 Study Execution & Oversight
- Monitor enrollment & trial performance
- Track operational issues & resolutions
- Support risk and quality management activities
- Ensure protocol & compliance adherence
💻 TMF, CTMS & EDC Activities
- Maintain CTMS, eTMF & EDC systems
- Manage trial documentation & reporting
- Ensure audit readiness & documentation accuracy
- Handle study-related system updates
🤝 Stakeholder & Vendor Management
- Collaborate with global clinical teams
- Coordinate with vendors & study sites
- Support communication and operational updates
- Monitor vendor setup & performance
⚙️ Process Improvement & Compliance
- Support CAPA implementation
- Participate in audits & inspections
- Contribute to automation & process optimization
📚 Learn CDISC Standards: CDISC SDTM & ADaM Guide
🎓 Qualifications & Eligibility
✅ Eligible Degrees
- B.Pharm / M.Pharm / Pharm.D
- BSc / MSc Life Sciences
- Clinical Research background
⭐ Required Experience
- 1–3 years experience in clinical trials / CRO / pharma industry
- Knowledge of CTMS, eTMF & EDC systems
- Understanding of global clinical trial workflows
💡 Required Skills
- Clinical operations knowledge
- Documentation & compliance understanding
- Risk management skills
- Strong communication & coordination abilities
- MS Office proficiency
🎁 Benefits & Career Growth
- Work with a global biotech leader
- Exposure to international clinical trials
- Career growth in Clinical Operations & Study Delivery
- Strong learning & development opportunities
- Collaborative & innovation-focused environment
📈 Explore Career Growth: Career Options After B.Pharm
🚀 Job Application Link
Carefully read the job description before applying. Knowledge of TMF, CTMS, EDC systems, and clinical trial coordination can significantly improve your chances of selection.
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