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Clinical Data Analyst II
Parexel
Bengaluru, IND
Full-time
Mid
Onsite
Discovered 1 weeks ago
Medidata RaveVeevaDataLabsClinBaseMedDRAWHODrug
Free
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Medidata RaveVeevaDataLabs
Role Overview
We are looking for a detail-oriented Clinical Data Analyst II to support clinical trial data management activities. The successful candidate will be responsible for managing, analyzing, and validating clinical trial data to support regulatory submissions and clinical research objectives. This role requires strong technical skills, attention to detail, and the ability to work independently while collaborating with cross-functional teams and study start-up support while ensuring compliance with ICH-GCP guidelines and industry standards.
Key Skills for This Role
Medidata RaveVeevaDataLabsClinBaseMedDRAWHODrug
Full Job Posting
Job Summary
We are looking for a detail-oriented Clinical Data Analyst II to support clinical trial data management activities. The successful candidate will be responsible for managing, analyzing, and validating clinical trial data to support regulatory submissions and clinical research objectives. This role requires strong technical skills, attention to detail, and the ability to work independently while collaborating with cross-functional teams and study start-up support while ensuring compliance with ICH-GCP guidelines and industry standards.
Key Responsibilities
- Perform clinical data validation: Extract, clean, validate, and reconcile clinical trial data from various sources.
- Manage data queries and support database lock activities.
- Review manual and system-generated data listings to identify discrepancies and ensure data quality. Identify and resolve data inconsistencies.
- Support the preparation and maintenance of Data Management documents and study-related records.
- Conduct User Acceptance Testing (UAT) for clinical database setups.
- Review study protocols, CRFs, and EDC screens when required.
- Track CRFs and support data entry activities as needed.
- Ensure adherence to SOPs, regulatory requirements, and ICH-GCP guidelines.
- Collaborate with cross-functional study teams and client stakeholders.
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