Key Responsibilities:

• Conducts site selection for potential sites to evaluate their capabilities for conducting a clinical trial.

•Performs site Initiation Visit, ensures site personnel is fully trained on all trial related aspects. Applies company policies and procedures to resolve a variety of issues •Frequent internal company and external contacts. Represents organization on specific projects.

• Contributes to some cost center goals and objectives

•Is the frontline liaison between Novartis and sites to ensure successful collaboration, site engagement and meeting Novartis expectation on milestone and deliveries.•Reporting of technical complaints / adverse events / special case scenarios related to Novartis products within 24 hours of receipt

Essential Requirements:

• At least 1-2 years Clinical Research Associate working experience or equivalence
• Operations Management and Execution
• Project Management
• Representing the organization
• Collaborating across boundaries
• English

Why Novartis: