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Principal Responsibilities:
- Collaborate with Functional Manager (FM)/Clinical Research Manager (CRM) for protocol and site feasibility.
- Lead local trial team to ensure quality data delivery on time and within budget.
- Manage adverse event reporting timelines and trial management systems.
- Monitor trial progress, initiate corrective actions, and communicate with study management teams.
- Assist in vendor selection, budget forecasting, and management.
- Conduct investigator meetings and oversee local trial team activities.
- Ensure compliance with local regulatory requirements and manage IEC/HA approvals.
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