长沙招聘

工作职责:

Position PurposeThe Sr. Associate, Information Management will contribute to the group’s activities of data analysis, business analysis, data quality, and report and metrics design in support of information aggregation and reporting services for the GPD, WRD organizations.

The role will utilize a broad range of skills, including eliciting business and data requirements, analyzing data, designing datasets, reports and visualizations, and developing queries and code in support of data aggregation, data standards and operational and regulatory reporting and analytics needs. The individual will be expected to learn and understand the set of supporting tools for performing job duties.

The role will assume advanced analytics work to gain business insights from various data sources within and outside the company.

Primary Responsibilities Participates in discussions with business partners to extract and document the requirements and critical business logic necessary for the data and reporting needs of the business lines.

Participates in the delivery of aggregated data, reports, metrics, analytics and/or visualizations in support of business requirements, following established methodologies and processes.

Conducts data analysis and investigations when issues with data are identified.

Collaborates to define and implement information standards and data quality measures to ensure data integrity and quality across functions. Supports the compliance of information with internal policies and external regulations and standards.

Proactively identify project and data issues and collaborate with the team to develop solutions

Proactively identify opportunities and conduct advanced analytics to deliver business insights.

Technical Skill RequirementsStrong data analysis skill is required - Advanced skills in SQL.

Experience with database/ETL development is required.Familiar with one or more databases - AWS Redshift, Impala/Hive, MySQL, Oracle, SQL Server, etc.

Familiar with one or more ETL tools - PipelinePilot, DataStage, Informatica

Experience with BI tools like Spotfire, Tableau, OBIEE etc. is preferred.

Experience with Alteryx development is preferred.

Alteryx certificate (Alteryx Designer Core/Advanced/Expert) is preferred

Strong oral and written English is preferred

Familiar with one or multiple programming skills is a plus – Python, Java"script", C#/.Net, Java, etc.

Exposure to big data/Cloud technologies is a plus – like Hadoop HDFS, Spark, AWS S3 etc.

Exposure to advanced analytics, AI/Machine learning is a plus.

Understand Pharm industry and GCP is a plus

Strong PM/BA skills is a plus

任职资格:

Qualifications (i.e., preferred education, experience, attributes)Minimum Bachelor’s degree in information technology, mathematics, statistics or other relevant STEM program, or equivalent experience in scientific computing, computational sciences, bioinformatics or other relevant experience.

Knowledge of project management, data analysis, business analysis, and information integration

Familiarity with Clinical, Safety, Regulatory and Content Management systems and processes

Demonstrated facility to understand the “big picture” in terms of potential implications, and translate to activities in support of the “big picture”

Demonstrated project management and organizational skills.

Demonstrated customer relationship skills and capabilities, and collaboration on teams.

Strong verbal, written communication and presentation skills.

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。