Amgen Hiring Data Management Associate & Sr Associate | Clinical Data Management Careers
Amgen, one of the world's leading biotechnology companies, is hiring for Data Management Associate and Data Management Senior Associate positions in Hyderabad. These opportunities are ideal for professionals with experience in Clinical Data Management, Global Clinical Trials, EDC Systems, Data Cleaning, Query Management, and Clinical Research Operations.
Selected candidates will contribute to global clinical development programs while working with advanced platforms such as Medidata Rave, Veeva Vault, and other clinical data management systems.
📋 Job Overview
| Details | Information |
|---|---|
| Company | Amgen |
| Location | Hyderabad, Telangana |
| Position 1 | Data Management Associate |
| Experience | 4+ Years |
| Position 2 | Data Management Sr Associate |
| Experience | 6+ Years |
| Industry | Clinical Research / Biotechnology |
| Employment Type | Full-Time |
🏢 About Amgen
Founded in 1980, Amgen is a global biotechnology leader focused on developing innovative therapies across Oncology, Inflammation, General Medicine, and Rare Diseases. The company supports millions of patients worldwide through cutting-edge science and clinical innovation.
📌 Data Management Associate Responsibilities
- Support clinical data management activities throughout study lifecycles.
- Assist in database build activities and edit check testing.
- Support laboratory data setup and medical coding activities.
- Perform data cleaning and query management.
- Participate in reconciliation and database lock preparation.
- Maintain CRF testing scripts and reconciliation trackers.
- Monitor data quality trends and identify issues.
- Collaborate with cross-functional study teams.
- Gain exposure to Veeva Vault and Medidata Rave.
📌 Data Management Sr Associate Responsibilities
- Execute clinical data management activities independently.
- Perform database build testing and validation.
- Manage data cleaning, reconciliation, and database lock preparation.
- Support Data Delivery Leads and Database Designers.
- Maintain EDC and non-CRF data structures.
- Coordinate with global teams and external vendors.
- Track study timelines and deliverables.
- Support coding dictionaries and laboratory integrations.
- Drive process improvement initiatives.
🎓 Eligibility Criteria
- B.Pharm
- M.Pharm
- Pharm.D
- B.Sc (Life Sciences)
- M.Sc (Life Sciences)
- Biotechnology
- Microbiology
- Biochemistry
- Clinical Research
- Nursing
- Biomedical Sciences
- Engineering
- Related Life Science Disciplines
Experience Requirements:
- Data Management Associate: Minimum 4 Years Experience
- Data Management Sr Associate: Minimum 6 Years Experience
- Clinical Research, CRO, Pharmaceutical or Biotechnology Experience Preferred
💡 Preferred Skills
- Clinical Data Management
- Query Management
- Data Cleaning
- Database Lock Activities
- Clinical Trial Operations
- Electronic Data Capture (EDC)
- Medidata Rave
- Veeva Vault
- Medical Coding
- Data Reconciliation
- Clinical Documentation
- Global Clinical Trials
- Data Quality Management
- Cross-functional Collaboration
- Regulatory Compliance
🎁 Employee Benefits
- Comprehensive medical insurance.
- Dental and vision coverage.
- Retirement and savings plans.
- Life and disability insurance.
- Annual performance bonus.
- Long-term stock incentives.
- Career development opportunities.
- Flexible work arrangements where applicable.
- Company-wide shutdown periods and paid time off.
📈 Why Consider a Career in Clinical Data Management?
Clinical Data Management professionals play a critical role in ensuring the accuracy, integrity, and compliance of clinical trial data. With increasing global clinical research activity, skilled professionals in Data Management, EDC Systems, Clinical Operations, and Data Quality are in high demand across CROs, pharmaceutical, and biotechnology organizations.
These Amgen opportunities provide exposure to global studies, advanced clinical systems, and long-term career growth within one of the world's leading biotechnology companies.
📄 Resume & Interview Preparation Tips
- Highlight Clinical Data Management experience and study support activities.
- Mention EDC platforms such as Medidata Rave, Veeva Vault, Oracle Clinical, or similar systems.
- Showcase Query Management, Data Cleaning, Reconciliation, and Database Lock experience.
- Include exposure to global clinical trials and regulatory compliance.
- Keep your resume ATS-friendly and achievement-oriented.
📝 How to Apply
- Select the position you wish to apply for.
- Read the complete job description carefully.
- Prepare an updated ATS-friendly resume.
- Complete the 15-second countdown timer to unlock the application button.
- Apply only if your experience matches the role requirements.
🚀 Select Position & Apply
⏳ Please wait... Unlocking Apply Button
We use a 15-second timer to encourage you to read the job description carefully before applying. Understanding the role increases your chances of success and helps create a strong professional impression.
.png)
