Study Start Up Manager at IQVIA managing site activation and regulatory activities for clinical studies. Collaborating with teams to ensure project compliance and timelines.
Responsibilities
Oversee the execution of Site Activation and/or Maintenance for assigned projects
Adhere to project timelines
Resolve project related issues where required
Requirements
Direct and manage the delivery of site activation, maintenance and regulatory activities
Develop, implement and maintain the Management Plan according to the Scope of Work and Project Plan
Ensure collaboration across Regulatory & Site Activation
Create and/or review technical and administrative documentation
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