1+ months

Technical Supervisor, IM

Hedgesville, WV 25427
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**Job Title:**

**Sr. Associate Information Management**


**Worldwide Research and Development (WRD) /** **GPD**


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


**IM Services** **(IMS) - China - Shanghai**

**Version Date:**

**19-** **Oct-2018**

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

+ Lead of Reporting Service IM 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 Clinical and Regulatory domain and value-added enabling shared services for the customers and solutions owned and managed by Information Management Reporting Service Team.

**Primary Responsibilities**

+ Provide operational Reporting Service support to business on 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.

**Technical Skill Requirements**

+ Minimum of 3 years BI development experience. Candidates with Safety data and business processes in the pharmaceutical industry, including an understanding of the drug development process are preferred.

+ 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.

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

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

+ Bachelor's Degree in information management related discipline required.

+ Knowledge of FDA, EMEA and ICH regulations is preferred.

+ 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.

Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.
Posted: 2020-10-13 Expires: 2020-12-13
Sponsored by:
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Technical Supervisor, IM

Hedgesville, WV 25427

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