Central Monitor Professional

Job description

• Contributes, with appropriate oversight, to all aspects of global clinical trial(s) to deliver study outcomes within schedule, budget, quality/compliance and performance standards. May lead specific aspects of global clinical trial process. Contributes to operational excellence through process improvement and knowledge sharing.

Major accountabilities:

• Might be involved in various operational excellence activities like process improvement or other line function initiatives.
• Reporting of technical complaints / adverse events / special case scenarios related to Novartis products within 24 hours of receipt -Distribution of marketing samples (where applicable)

Key performance indicators:

• Timely, efficient and quality execution of trials & trial related activities within assigned clinical program(s) within budget, and in compliance with quality standards.
• Adherence to Novartis policy and guidelines and external regulations.

Minimum Requirements:

Work Experience:

• Financial Management.
• Critical Negotiations.
• Collaborating across boundaries.
• Operations Management and Execution.

Skills:

• Budget Management.
• Clinical Trials.
• Negotiation Skills.
• Process Improvement.
• Project Management.
• Project Planning.
• Vendor Management.