Job DescriptionJD 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. N
- Maintain study trackers, reports, and study documentation. N
- Coordinate with CROs and vendors to ensure study deliverables. N
- Manage TMF and study-related documents. N
- Track study progress, metrics, and compliance issues. N
- Ensure adherence to ICH-GCP, SOPs, and regulatory requirements. N
nMust-Have Skills:
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- Clinical Trial Operations N
- Study Management Support N
- TMF Managementn
- CRO/Vendor Coordination N
- ICH-GCP Knowledgen
- Documentation & Reporting N
- Communication Skills N