Expert Statistical Analyst - Site Coordinator and Analysis Expert

Major Responsibilities

• Provide coordination for the Statistical Programming at the Beijing site
• Participate in the planning process for Statistical Programming function to ensure transparency of workload to enable effective resource allocation within site and across region(s)
• Establish effective, collaborative interfaces with partners in Clinical Development (Therapeutic Area Clinicians, Medical Writing) and with partners outside Clinical Development (Data Management, Regulatory, O&I, Marketing)
• Participate in the process of Recruiting, Hiring and training of staff.
• Act as a mentor for statistical programmers
• Independently seek out and develop a broad knowledge of submission requirements (CDISC, FDA, EMEA, SFDA, PMDA, other health authorities in the region) and communicate/train others in the function on this information. 
• Participate in industry meetings, professional and scientific groups/events with regard to new technologies and be an expert responsible for communication and training of internal/external analysts on these technologies
• Provide support for all statistical programming system and operations processes at the site/region.
• Member of Global Statistical Programming and Biostatistics Operations Leadership Team

Requirement

• MS or PhD in Statistics, Mathematics, Computer Science
• Five years experience in statistical programming and submission preparation in pharma or biotech. Two to Three years of experience as a project leader in a global organization