请帮我用英文润色下如下的简历要求是更加专业化Zhitao PanCareer ObjectiveTo seek a leading position of clinical programming in clinical trials in a CRO or pharmaceutical companyEducationFudan University School of Public Healt

Zhitao Pan

Career Objective To obtain a leading position in clinical programming for clinical trials within a CRO or pharmaceutical company.

Education Fudan University, School of Public Health, Shanghai, China Jun, 2003 Master of Science, Epidemiology and Health Statistics Shandong Medical University, School of Public Health, Jinan, Shandong, China Jun, 2000 Bachelor of Science, Preventive Medicine

Work Experience Pfizer China Research & Development Center, Shanghai, China May, 2005 – Aug, 2016 Positions Held: Apr, 2015 - Aug, 2016 Associate Director, Clinical Programming Apr, 2012 - Mar, 2015 Senior Manager, Clinical Programming Feb, 2010 - Mar, 2012 Manager, Clinical Programming
Aug, 2008 - Jan, 2010 Senior Supervisor, Clinical Programming
May, 2005 - Jul, 2008 Clinical Programmer
Responsibilities: • Managed a team of 30+ clinical programmers focusing on therapeutic areas including CVMET, Oncology, I&I, and rare disease. Oversaw all SAS programming and related activities for clinical studies involving investigational products at various phases. Performed SAS programming tasks and acted as the primary point of contact for SAS programming activities to ensure adherence to guidelines, methodology, and SOPs for software and program development in accordance with FDA, ICH, GCP, and SDLC. Actively defined and managed programming timelines for different reporting deliverables both at asset and study level. Provided programming oversight to ensure timely and quality clinical data and analysis deliverables enabling successful studies, submissions, and commercialization. • Developed junior programmers and fresh students into senior clinical programmers and competitive programming supervisors. Provided timely feedback and effective mentoring to direct and indirect reports in a positive manner. Held direct and indirect reports accountable for their deliverables and performance. Encouraged open discussion and straight talk to solve problems based on facts and considering multiple aspects. • Aligned the team's programming work to departmental business goals as well as division and business unit's goals. Actively led, coordinated, developed, and participated in diversified departmental and corporate initiatives. Assisted the department head in developing holistic and long-term programming strategies based on internal and external factors. Proactively cooperated with colleagues within and outside of Pfizer CRDC to facilitate processes in clinical trials. Provided timely and quality support to other functional lines where needs were required. • Developed and maintained superb work relationships with customers and stakeholders within and outside of Pfizer. Achievements: • Successfully completed 200+ work requests and/or clinical studies since joining Pfizer CRDC in 2005. • The most stable programming group lead within CPW (Clinical Programming and Writing), Pfizer CRDC due mainly to outstanding people management skills and extraordinary personal leadership behaviors. • Received extremely positive feedback frequently from clinicians, statisticians, clinical pharmacology leads, and other key customers. • The programming lead for SGLT-2 inhibitor – Ertugliflozen (for the treatment of type II diabetes), the first positive POC (proof of concept) in Pfizer CRDC. • The programming lead for 2 other positive POC assets: PCSK9 inhibitor bococizumab (for the treatment of hyperlipidemia) and HER2/neu receptor inhibitor Trastuzumab (Pfizer’s 1st investigational product in biosimilars for the treatment of advanced breast cancer). • The programming coordinator for an ongoing phase III pivotal study – Infliximab Pfizer in Biosimilars –in patients with rheumatoid arthritis (RA). The candidate met its primary endpoint demonstrating equivalent efficacy with comparator Remicade according to ClinicalTrials.gov on 17Sep2016. • The internal task force lead for the internal Programming Interest Group since 2008. • The co-lead of programming recruitment and training as a result of significant programming expansion in CPW, Pfizer CRDC.

EPS China Co., Ltd., Shanghai, China Jul, 2003 – May, 2005 Positions Held: Jul, 2003 – May, 2005 Biostatistician Responsibilities: Drafted and optimized internal SOPs; Drafted, revised, and finalized statistical analysis plans (SAP) for clinical studies; Developed SAS programs and produced TLFs (tables, listings, figures) for clinical studies; Provided customers with statistical analyses and helped explain study results in clinical fields; Performed logic checks by means of programming and sent out query forms to customers. Achievements: Helped draft and finalize several internal SOPs for the database management system; Developed and maintained a couple of standard SAS programs, which significantly improved the whole efficiency of statistical programming; Completed several clinical studies successfully with excellent customer feedback; Won first place in 2004 English training test within the company.

Self-Assessment Passionate about clinical development; Honest and broad-minded; Accountable and detail-oriented; Strives to be impactful by helping others find more effective solutions; Seeks first to understand, then to be understood