Senior Analyst, DA DS&M Data Acquisition
GSK (company site, opens in a new tab)5+ yrsBengaluruOn-siteDirect career pageEst. 12–20 LPA
Posted 8h ago
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Job description
Structured overview of role & requirements
About This Role
- Own study set-up and technical development of eDC applications, including forms, validation checks, data extraction and associated documentation; deliver to quality and schedule.
- Coordinate data-acquisition specifications and vendor deliverables, resolve study data-acquisition issues, and provide status, risks and advice to Study Data Managers.
- Support delivery across clinical studies, including quality control, junior staff support, process improvements and after-action reviews.
Minimum Requirements
- Work Experience Required: 5+ years in data acquisition or related work in Clinical Research, Information Systems and/or relevant scientific experience.
- Experience with eDC solutions; examples named include Inform, Rave and Veeva CDMS Vault. ePro experience is also specified.
- Extensive working knowledge of GxP, ICH requirements, and applicable internal processes and external drug-development regulations.
- Knowledge of multiple programming languages, with examples including PL/SQL, SAS, Python and C#.
Ideal Candidate Profile
- Has clinical-study data-acquisition experience spanning study set-up, eDC development and coordination of vendors or multiple data types.
- Can manage study deliverables across studies of varying phase and complexity, with attention to quality, timelines, risks and issue resolution.
- Fits an environment that requires regulatory-aware execution and contributes operational learnings, process improvements and support for junior staff.