Amgen Hiring Data Management Associate

Amgen harnesses the best of biology and technology to fight the world’s toughest diseases, and make people’s lives easier, fuller and longer. We discover, develop, manufacture and deliver innovative medicines to help millions of patients. Amgen helped establish the biotechnology industry more than 40 years ago and remains on the cutting-edge of innovation, using technology and human genetic data to push beyond what’s known today.

Post : Data Management Associate

Data Management Associate
Job Description
• Support execution of core data management activities across the study lifecycle, including database build, edit check testing, lab and coding setup, data cleaning, query management, reconciliation, and lock preparation.
• Provide hands-on, flexible support across build, conduct, and closeout phases, developing broad exposure to end-to-end data management processes and study delivery.
• Deliver accurate and timely completion of assigned tasks, eg query management in support of Data Delivery.
• Assist in the preparation and maintenance of study documentation, including CRF testing scripts, reconciliation trackers, and lock readiness materials.
• Monitor data quality and query trends, proactively identifying issues, escalating where appropriate, and contributing to practical solutions.
• Collaborate cross-functionally when required, building proficiency in EDC systems (e.g., Veeva Vault, Medidata Rave) and other data management tools.
Candidate Profile
• Bachelor’s degree with 4 years of clinical execution experience
• 2 years' work experience in life sciences or medically related field, including 1 years of biopharmaceutical clinical research experience obtained working on clinical trials in a biotech, pharmaceutical or CRO company
• Experience working in Data Management on global clinical trials

Data Management Associate
Job Description
• Execute study data management tasks including database build testing, data cleaning, query management, reconciliation, and lock preparation with limited oversight
• Support core Data Management roles, such as Data Delivery Leads, Database Designers, and Data Acquisition Leads by owning time-sensitive deliverables with high-quality execution
• Actively contribute to setup and maintenance of EDC/non CRF data structures including local labs, coding dictionaries, along with non-CRF data integrations
• Track progress against data management timelines, study timelines and deliverables, identify risks or delays, and escalate issues with clear documentation and any mitigations
• Coordinate with local internal teams, global team members as well as external partners (including FSPs) when required to ensure aligned and efficient delivery of all study activities
• Identify opportunities to improve repeatable processes and contribute to best practices and knowledge sharing across the team
Candidate Profile
• Master’s degree OR
• Bachelor’s degree and 2 years of clinical execution experience OR
• Associate’s degree and 6 years of clinical execution experience OR High school diploma / GED and 8 years of clinical execution experience
• 3 years' work experience in life sciences or medically related field, including 1 years of biopharmaceutical clinical research experience obtained working on clinical trials in a biotech, pharmaceutical or CRO company
• Experience working in Data Management on global clinical trials

Career Category : Business Development, Clinical Development

Additional Information
Experience : 2 - 4 years
Qualification : Master’s degree, Bachelor’s degree
Location : Hyderabad
Industry Type : Pharma/ Healthcare/ Clinical research
End Date : 30th June 2026