长沙招聘

工作职责:

Job Title:

Sr. Associate Information Management

Division/Organization:

Worldwide Research and Development (WRD) / GPD

Line:

Information Management (IM), Operations Center of Excellence (COE)

Department:

IM DAR – China – Shanghai

Version Date:

24-Nov-2020

Organizational Relationship(s) including to whom the position reports (JD Job Title):

Lead of IM-DAR-Safety DRMT Shanghai Site

The position maps up to supervisor level, specific level placement is based on the years of experience and skills

Position Purpose

Individuals filling the positions listed are responsible for one or more of the responsibilities as providing high quality, predictable and cost effective business analysis/support, ad-hoc and scheduled data requests and report coordination for Drug Safety domain and value-added enabling shared services for the customers and solutions owned and managed by Information Management DAR Team.

Primary Responsibilities

Provide operational Reporting Service support to business on Drug Safety domains.

Develop and execute ad hoc or standard queries/reports and follow established procedures to validate queries/results based on business requirements

Provide analysis/consultant for business requirement, give solution and implement the solution

Participate in developing and performing User Acceptance Testing (UAT) as required.

Provide documentation support (e.g., format, link, version control etc.) to meet Pfizer’s standard and compliance requirements.

Participate in continued improvement activities on identifying competitive operational services to release burden on the IM and business colleagues.

Complete training in accordance with Pfizer’s and GPD COE Information Management curriculum.

任职资格:

Technical Skill Requirements

Minimum of 3 years BI development experience.

Strong capability on Business Analysis, Project Management and Documentation

Familiar with at least one BI reporting tool listed below. Experience on data model design, dashboard, report and analysis development, publishing, etc.SAP Business Objects

Crystal Report

Spotfire

Tableau

Familiar with Oracle databases

Familiar with query tools/data extraction techniques (e.g., SQL, PL/SQL, SQL Plus)

Familiar with Microsoft word & excel, Adobe acrobat, etc.      

Candidates with Safety data and business processes in the pharmaceutical industry, including an understanding of the drug development process are preferred.

Knowledge of Clinical, Drug Safety, and Regulatory is preferred.

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

Bachelor’s Degree in information management related discipline required. 

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.

Knowledge of FDA, EMEA and ICH regulations is preferred.

Candidates with Japanese language skills is preferred.

Technical Skill Requirements

Minimum of 3 years BI development experience.

Strong capability on Business Analysis, Project Management and Documentation

Familiar with at least one BI reporting tool listed below. Experience on data model design, dashboard, report and analysis development, publishing, etc.SAP Business Objects

Crystal Report

Spotfire

Tableau

Familiar with Oracle databases

Familiar with query tools/data extraction techniques (e.g., SQL, PL/SQL, SQL Plus)

Familiar with Microsoft word & excel, Adobe acrobat, etc.      

Candidates with Safety data and business processes in the pharmaceutical industry, including an understanding of the drug development process are preferred.

Knowledge of Clinical, Drug Safety, and Regulatory is preferred.

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

Bachelor’s Degree in information management related discipline required. 

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.

Knowledge of FDA, EMEA and ICH regulations is preferred.

Candidates with Japanese language skills is preferred.

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。