Job Description & How to Apply Below
As the Clinical Evidence Project Manager, you will be instrumental in collaborating with the Client Associate Director on the oversight of pivotal evidence studies. The ideal candidate will possess strong project management capabilities and a comprehensive understanding of clinical systems, ensuring projects meet quality, time, and cost standards while supporting continuous improvement.
Key Responsibilities:
• Ensure successful execution of observational and externally sponsored studies
• Coordinate with cross-functional internal and external teams
• Maintain compliance with all regulatory requirements
• Engage in continuous improvement of medical evidence delivery
• Produce and refine guidance materials and training resources
Requirements:
• Bachelor’s degree and 2+ years in Biotech, Pharma, or CRO
• Strong project management experience in initiation phases
• Expertise in Phase IV Interventional studies
• Ability to drive vendor management and data enhancements
• Strategic insight into clinical study development
Join ICON in making a real impact on global healthcare through clinical evidence studies.
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