Job Description

We're committed to delivering medicines to the world with greater speed, without compromising on excellence and integrity. Navigating both local and global regulations is crucial, and the dynamic regulatory landscape demands innovative thinking and meticulous attention to detail. Your contributions will ensure that our products meet the highest standards of regulatory compliance, ultimately helping patients receive the treatments they need more efficiently.
Job Summary
Regulatory Project Associate role provides both operational and coordination support to the GRS-RIO-EM organization.
As needed, will also support with special projects (in-country, regional, regulatory initiatives within the organization)
Job Responsibilities
Regulatory Coordination Support
Preparation and management of relevant monthly reports and communications.
Analytical and operational related support for related systems/processes (including SPA reporting, RRM maintenance, CST requests, Veeva,...

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