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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