JD 1: Clinical Study Management Support Specialist
nRole: Clinical Study Management Support Specialist
nResponsibilities:
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- Support global clinical studies across start-up, conduct, and close-out phases.
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- Maintain study trackers, reports, and study documentation.
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- Coordinate with CROs and vendors to ensure study deliverables.
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- Manage TMF and study-related documents.
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- Track study progress, metrics, and compliance issues.
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- Ensure adherence to ICH-GCP, SOPs, and regulatory requirements.
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nMust-Have Skills:
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- Clinical Trial Operations
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- Study Management Support
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- TMF Management
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- CRO/Vendor Coordination
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- ICH-GCP Knowledge
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- Documentation & Reporting
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- Communication Skills
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