Responsible for the end-to-end operational management of clinical trials across sites and geographies. Ensures trials are delivered on time, within budget, and in compliance with GCP.
Manage day-to-day operations of Phase I–III clinical trials Select, initiate, and oversee clinical investigator sites Monitor patient recruitment, data quality, and protocol compliance Manage CRO and vendor relationships Track trial budgets, timelines, and risk registers Ensure compliance with ICH-GCP, FDA, EMA regulations Prepare and review clinical study reports (CSRs)
Mandatory Skills
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