长沙招聘

工作职责:

Primary Responsibilities  

Develop and maintain suite of reporting solutions to serve the Regulatory organization and supporting business lines  

Liaise with business and technical groups to define or gather business requirements, define new business and support processes or improve existing processes  

Provide data analysis support ongoing to key stakeholders for regulatory data 

Liaise with business stakeholders and technical groups to define or gather data integration, automation, or reporting requirements and execution strategy 

Participate in and lead quality-oriented projects intended to ensure high quality data in our regulatory tracking systems 

Lead small projects of short duration, following established methodologies  

Provide solutions to customer data issues and develop or contribute to written materials that communicate solutions and/or options to relevant stakeholders 

Support continuous improvement projects to simplify and improve system use and system management, including opportunities for data automation and system integrations 

Develop and execute ad hoc or standard queries to extract data from supported systems and follow established procedures to validate queries/results in support of business requirements 

Define data standards and quality measures in partnership with supporting business lines 

Develop monitoring reports to ensure proper system usage and data standards alignment 

 

 

Resources Managed (budget and FTEs) 

No direct reports - this role is an individual contributor role.  Potential matrix management of cross-functional teams. 

 

任职资格:

Qualifications (i.e., preferred education, experience, attributes) 

 BASIC QUALIFICATIONS  

Bachelor’s Degree in life sciences, information management, library science, information technology, computer science, business administration or related discipline or 5+ years’ experience in Pharmaceutical industry or in a data analysis and reporting role   

Knowledge of Pharmaceutical metadata and standards  

Strong analytical and critical thinker with the ability to solve issues and communicate findings 

Demonstrated customer relationship skills and capabilities and collaboration on teams. 

Demonstrated ability to perform in a cross-functional environment.  

Strong verbal, written communication and presentation skills. 

Strong demonstrated project management and organizational skills 

Experience with systems management and maintenance including document management systems, databases, business process management and electronic workflow/routing tools, regulatory submission and tracking systems 

Technical aptitude for learning new applications and data models  

Ability to interact in a professional manner and build strong collaborative relationships with internal Pfizer teams. 

Good working knowledge of MS Office Programs – Excel, PowerPoint, Word and Outlook 

Experience with data analysis and reporting techniques and technologies (e.g., SQL, PL/SQL, Brio, MS_Access, Spotfire, Pipeline Pilot) 

 

PREFERRED QUALIFICATIONS 

Master’s Degree in life sciences, information management, library science, information technology, computer science, business administration or related discipline   

Understanding of the drug development process and regulatory interactions within the pharmaceutical industry 

On October 31, 2005, Pfizer announced the official opening of China Research and Development Center (CRDC) in Shanghai. Pfizer Global Research and Development’s Center is mainly engaged in drug development activities. Much of the facility's capacity is devoted to the study design, data management and statistical analysis of global phase I-IV clinical trials, as well as the clinical study report process. In addition, CRDC is a part of Pfizer global Safety and Risk Management and covers the functions of safety data processing and assessment. The center also trains Pfizer employees in China and throughout the Asia region in internationally recognized Good Clinical Practice standards.
辉瑞公司于2005年10月31日宣布辉瑞中国研发中心正式在上海揭幕。辉瑞中国研发中心主要为全球辉瑞药物开发提供支持工作。大部分的功能是围绕在I-IV期临床试验研究设计、数据管理和生物统计分析、以及临床试验报告的部分准备工作。此外，该中心是辉瑞全球安全和风险管理部的一个分支，负责安全数据处理和评估工作。研发中心还将为辉瑞公司在中国及亚洲的其它运营部门的员工提供国际标准的临床试验管理规范(GCP)的技术培训。