our client is an Innovative Drug Company,is located in Zhangjiang Hi-Tech park, Pudong, Shanghai. The shareholders of the company are well-known companies and universities.

• Liaises with other functional groups to ensure the study members and monitors receive appropriate therapeutic area and study specific training.
• Prepare and conduct outsourcing vendor(CRO)selection. Act as a key contact with outsourcing vendor for proposal,interview,evaluation and contract negotiation.
• Supervise the conduct of the study is in accordance with quality plan:ensure studies are performed in compliance with protocol,ICH-GCP guidelines,FDZJ SOPs,local operating guidelines and all applicable regulatory requirements and quality plan.

Education and Work Experience Requirement:
• At least 3 years' clinical development experience on the operational aspects of conducting clinical studies including vendor/CRO management,leading/working as part of a development team, implementing clinical development plans and coordinating study level activities to deliver data for filing or publication purposes including interaction with local Business Units.
• Experience influencing and negotiating at all levels to achieve team delivery.
• International travel required when needed.