Sr Data Management Support What you will do

Lets do this. Lets change the world. In this vital role you will support the delivery of high-quality clinical trial data by executing core data management activities across the study lifecycle, ensuring data integrity, compliance, and timely study execution.

- 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 productive delivery of all study activities
- Identify opportunities to improve repeatable processes and contribute to best practices and knowledge sharing across the team

Basic Qualifications
- Bachelors degree with 6 years of clinical execution experience

Preferred Qualifications
- 3 years' work experience in life sciences or medically related field, including 1 year 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 Sr Associate (Telangana)
🏢 Amgen
📍 Telangana