Amgen Hiring Study Delivery Associate | Clinical Research & eTMF Jobs in Hyderabad
Amgen is hiring Study Delivery Associate for its Clinical Development team in Hyderabad.
This opportunity is ideal for candidates from B.Pharm, M.Pharm, Pharm.D, BSc, MSc, and Life Sciences backgrounds interested in careers in Clinical Operations, Study Coordination, CTMS, eTMF Management, and Global Clinical Trials.
📋 Job Overview
| Details | Information |
|---|---|
| Job Role | Study Delivery Associate |
| Company | Amgen |
| Department | Clinical Development |
| Location | Hyderabad |
| Job Type | Full-Time |
| Work Mode | On Site |
| Qualification | B.Pharm, M.Pharm, Pharm.D, BSc, MSc, Life Sciences |
| Experience | 1–2 Years Preferred |
📌 Key Responsibilities
- Support study timelines, dashboards, and trackers
- Assist in clinical trial documentation and submissions
- Manage CTMS, eTMF, and study-related systems
- Support investigator meeting logistics and study start-up activities
- Coordinate investigational product logistics and biological sample management
- Assist with trial risk management and quality review documentation
- Support inspection readiness and regulatory compliance activities
- Maintain accurate clinical trial data entry and system updates
- Support vendor coordination and site engagement activities
- Ensure protocol adherence and document version control
🎓 Eligibility Criteria
- B.Pharm / M.Pharm / Pharm.D candidates can apply
- BSc / MSc Life Sciences candidates eligible
- 1–2 years of Clinical Research or Biotech industry experience preferred
- Knowledge of CTMS, eTMF, and EDC systems beneficial
- Understanding of Clinical Trial documentation required
- Good MS Excel, Word, and PowerPoint skills preferred
- Strong communication and coordination abilities important
- Knowledge of GCP and inspection readiness preferred
⭐ Preferred Skills
- Clinical Trial Operations
- eTMF Management
- CTMS Handling
- Study Coordination
- Vendor & Site Coordination
- Regulatory Documentation
🌍 Why Join Amgen?
- Opportunity to work on global biotech clinical trials
- Exposure to advanced Clinical Development programs
- Strong career growth in Clinical Operations
- Learning and development opportunities
- International work culture and collaboration
- Health and wellness employee benefits
📄 Resume Tips
- Highlight CTMS, eTMF, or clinical documentation exposure
- Mention Clinical Research projects and internships clearly
- Add GCP and Clinical Trial Operations knowledge
- Showcase coordination and communication skills
- Use ATS-friendly resume formatting
- Keep resume concise and professional
🎯 Interview Tips for Study Delivery Associate Role
- Revise CTMS, eTMF, and Clinical Trial basics thoroughly
- Understand Study Start-Up and Trial Coordination workflows
- Prepare GCP and inspection readiness concepts
- Practice documentation and compliance-related questions
- Be ready to explain previous Clinical Research experience
- Research Amgen and global biotech clinical operations
- Prepare examples showing teamwork and coordination skills
- Maintain professional communication during interviews
❓ Frequently Asked Questions (FAQs)
1. What is the job location?
The job location for this role is Hyderabad.
2. Which qualifications are eligible?
B.Pharm, M.Pharm, Pharm.D, BSc, MSc, and Life Sciences candidates are eligible.
3. Is prior Clinical Research experience required?
Yes, candidates with 1–2 years of Clinical Research or biotech industry experience are preferred.
4. What systems knowledge is preferred?
Knowledge of CTMS, eTMF, and EDC systems is beneficial for this role.
5. What is the estimated salary?
The estimated salary for this role is around ₹5.5 – ₹9 LPA.
🚀 Job Application Link
Please make sure to read the complete job description carefully before submitting your application. Make sure your qualifications, clinical operations experience, and CTMS/eTMF knowledge align with the role requirements.
