Clinical Trial Project Specialist ( Up 6 K ) #HVN

About this role

Responsibilities • To oversee full study lifecycle from planning tocloseout. • To act as primary liaison between the clinicalresearch sponsors ethics boards, and monitors. • To lead protocol development to ensureoperational feasibility. • To manage study documents, risk mitigation,safety oversight,

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• Consulting
• Customer Service
• Healthcare / Pharmaceutical
• Sciences / Laboratory / R&D
• Document Management
• Preparation of Test Plan
• Vendor Development
• Time Study

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