When our values align, theres no limit to what we can achieve. At Parexel, we all share the same goal - to improve the worlds health. From clinical trials to regulatory, consulting, and market access, every
Overview As a Senior Regulatory Affairs Associate, you will drive post-approval regulatory activities focused on CMC for biological and vaccine products. You will collaborate across manufacturing, QA, QC, and regulatory teams to shape submission strategies and ensure worldwide
The selected post-doc is expected to generate different MAPS, by evaluating the most appropriate chemistry for all GBS polysaccharides to be included in the vaccine. She/he will characterize them, evaluate their purity, initial stability and test them
Parexel FSP is hiring for two experienced CRAs at either the CRA II or Senior CRA level to join one of a large Sponsor’s in the EU. This role is responsible for the site management, site
Parexel International is seeking a Senior Regulatory Affairs Associate to join our team on a client-dedicated project. This role focuses on post-approval CMC regulatory activities for biological and vaccines products, with options for office or home-based work across
Job Description: Within the Policy & Communications Department, we are seeking a proactive, dynamic, and results-oriented professional to support the Associate Director, Policy & Government Relations in advancing the companys policy priorities and institutional engagement agenda, as