Clinical Project Manager

Major Responsibilities：

• Decide sites for local/regional trials; analyze capability and make recom-mendation for trial inclusion.
• Assume ambassadorial role to facilitate communication between sites and Novartis line functions and increase value proposition to investigators.
• Facilitate preparation and collection of trial documents; resolve problems as required.
• Supervise trial implementation from project management point of view.  Coaching CRO CRA with regard to site initiation, monitoring visits, closeout activities, regulatory assessment, and resolution of site problems to ensure compliance. 
• Track trial execution milestones; identify problems; resolve issues and escalate as appropriate.
• Manage recruitment and execute contingency plans, as needed.
• Provides operational input to Clinical Trial Protocols, CRFs and Data Man-agement meetings as required
• Act as local/regional trial lead. Be responsible for CRO selection for lo-cal/regional trials.
• Act as a mentor to in-sourced CRA for purposes of field training, as as-signed. Participate in multi-disciplinary teams within CPO to evaluate and imple-ment process improvement.

Requirement：

• BS or higher degree with medical or pharmacological background
• Fluent English (oral and written)
• At least 5 years clinical trial experience in multi-national pharmaceuticals company