Clinical Data Coordinator
ICON plc (company site, opens in a new tab)ChennaiOn-siteDirect career pageEst. 4–8 LPA
Posted 14h ago
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Job description
Structured overview of role & requirements
About This Role
- Support the Data Management Study Lead by maintaining eCRFs, data validation specifications, and study-specific procedures.
- Reconcile clinical and third-party data against edit specifications and data review plans; investigate data issues and recommend solutions.
- Track and communicate study/task metrics and help resolve data issues by identifying root causes.
Minimum Requirements
- Work Experience Required: Relevant clinical data management experience; duration not explicitly mentioned in the JD.
- Bachelor’s degree in a relevant field, such as Life Sciences or Healthcare.
- Intermediate clinical data management knowledge in the pharmaceutical or biotechnology industry, plus familiarity with systems such as Medidata or Oracle RDC.
- Must have the legal right to work in the country where the role is based.
Ideal Candidate Profile
- Has practical clinical data management exposure in a pharmaceutical or biotechnology setting and can work with clinical and third-party data.
- Can maintain study data-management documentation and systems while following study specifications and review plans.
- Experience identifying data issues, investigating root causes, and reporting study/task status to project and functional stakeholders is a strong fit.