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