We are looking for a Data Coordinator Clinical Data Management to support the end-to-end clinical trial data management lifecycle, from study start-up through database lock and study close-out.
The successful candidate will work under the direction of the Clinical Data Management (CDM) Lead and contribute to the delivery of high-quality, accurate, and timely clinical trial data in accordance with applicable SOPs, processes, and regulatory requirements.
Key Responsibilities
Clinical Data Review
- Perform review of clinical trial data for completeness, accuracy, and consistency.
- Identify data discrepancies and support query generation, tracking, and resolution.
- Review clinical data according to study-specific requirements and CDM processes.
- Perform data cleaning activities and follow up on outstanding data issues.
Data Reconciliation
- Perform reconciliation of external data against EDC data.
- Identify discrepancies between EDC and external data sources and coordinate appropriate resolution.
- Support reconciliation activities throughout the clinical trial lifecycle.
Study Support
- Support clinical data management activities from study start-up through database lock and study close-out.
- Assist in the preparation and maintenance of study-related documentation.
- Assist with study reports, data listings, metrics, and other CDM deliverables.
- Support the CDM Lead with study-specific data management activities.
Compliance & Quality
- Perform activities in accordance with applicable SOPs, work instructions, study protocols, and CDM processes.
- Maintain data quality and ensure activities are completed within established timelines.
- Support audit and inspection readiness activities as required.
📌 Clinical Data Coordinator (India)
🏢 Siro Clinpharm
📍 India
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