Clinical Research Associate (Multiple Positions)

Summary

Monitor patient data and learning related information for clinical research sites and trial participation, ensuring investigators comply with protocols, regulatory requirements, and Good Clinical Practice. Provide timely and accurate monitoring from source documents, study records, and site visits (if applicable). Monitor site selections and audit facility choices.

About the Role

• Perform site selection to assess capability to conduct clinical trials.
• Conduct site initiation visits to ensure all trial-related aspects are adequately trained.
• Apply company policies and procedures to solve various issues.
• Maintain frequent internal and external communication representing the organization for specific projects.
• Commit to achieving various cost-centered goals.
• Act as the frontline liaison between Novartis and sites to ensure successful collaboration, site engagement, and meeting expectations for...