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 transparent 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 prospects to improve repeatable processes and contribute to best practices and knowledge sharing across the team
What we expect of you
We are all different, yet we all use our unique contributions to serve patients. The candidate we seek is an individual with the following qualifications.
Basic Qualifications:
Masters degree OR
Bachelors degree and 2 years of clinical execution experience OR
Associates degree and 6 years of clinical execution experience OR High school diploma / GED and 8 years of clinical execution experience
Preferred Qualifications:
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
📌 Data Management Sr Associate Telangana
🏢 AMGEN
📍 Telangana
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