Manager, IM
Shanghai, Shanghai , China

Manager, IM

  • China - Shanghai - Shanghai
  • 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 leadquality-orientedprojects intended to ensure high quality data in our regulatory tracking systems

    Lead small projects of short duration, following established methodologies

    Providesolutions tocustomer data issues and develop or contributeto 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 queriesto extract data from supported systemsand 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.

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


    Bachelor’s Degree in life sciences, information management, library science, information technology, computer science, business administration or related discipline or 5+years’ experiencein 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)


    Master’sDegree in life sciences, information management, library science, information technology, computer science, business administrationor related discipline

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

    Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.

    Information & Business Tech


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