Job Title:

Associate Information System Coordinator / Business Analysis

Division/Organization:

Pfizer Research and Development (PRD) / Clinical Development & Operations (CD&O)

Line:

Information Management (IM)

Department:

IM Safety Solutions (IMSS) - China - Shanghai

Version Date:

16-Dec-2024

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

• Lead of Safety Solutions IM Shanghai Site
• The position maps up to Senior Supervisor/Manager level, specific level placement is based on the years of experience and skills

• 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, Safety System support and project coordination for Safety domain and value-added enabling shared services for the customers and solutions owned and managed by Safety Solution Team.

• Provide support to business on drug safety domains and systems.
• Provide Japan, China and Global support for local Drug Unite based on regulatory requirements.
• Provide analysis/consultant for business requirement, give solution and implement the solution
• Participate in developing and performing User Acceptance Testing (UAT) as required.
• Develop and execute ad hoc or standard queries/reports and follow established procedures to validate queries/results based on business requirements
• 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 PRD CD&O Information Management curriculum.

• Minimum of 3 years enterprise service application support and management experience. Candidates with Safety data and business processes in the pharmaceutical industry, including an understanding of the drug development process are preferred.
• Familiar with software development life cycle, strong capability on project planning, coordination and testing
• Strong Japanese communication skills
• Strong English communication skills
• Strong capability on Business Analysis, Project Management and Documentation
• Familiar with Microsoft word & excel, Adobe acrobat, etc.
• Familiar with Oracle databases is preferred.
• Familiar with at least one BI reporting tool listed below. Experience on data model design, dashboard, report and analysis development, publishing, etc. is preferred
  • SAP Business Objects
  • Crystal Report
  • Spotfire
  • Tableau
• Knowledge of Clinical, Safety, and Regulatory is preferred.

• Bachelor's degree in information management related discipline required.
• Familiar with Argus Safety and Understand Argus Database Structure is preferred.
• Knowledge of PMDA, CNDA, 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.