Responsibilities

• Supervise all aspects of designated clinical protocol with accountability of meeting agreed timelines, budgets, and performance quality;
• Create and maintain laboratory manuals (general and study-specific) and other study- related documents;
• Develop and present clinical laboratory presentations at investigator meetings;
• Design specifications and monitor production of specimen collection kits;
• Serve as primary contact for Sponsors regarding all aspects of assigned protocol(s);
• Track study status as appropriate;
• Communicate all aspects of protocol to various internal departments for appropriate study setup, maintenance, and closeout; and
• Write, establish, and revise relevant Standard Operating Procedures and/or work instructions; and
• Occasional handling of biological samples is a possibility

Qualifications

• Bachelor's degree in science or a health-related field;
• Knowledge of Microsoft Office;
• 1 - 3 years of project management experience in a clinical laboratory;
• Must have excellent oral and written communication skills.

Song Zhao Hui EA License No. 02C3423 Personnel Registration No. R1761205

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