parexel

Parexel FSP is hiring for two experienced CRA's 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 monitoring and close-out of assigned clinical trials investigator sites to ensure patient safety and quality study executionSome Specifics About This Advertised RoleEnsure...

Parexel International is seeking a Regulatory Affairs Consultant to lead post-approval activities focused on CMC for vaccines or biologics. The role allows office or home-based work across Europe.You will develop submission strategies, assess change controls, coordinate cross-department submissions, and manage information management systems. Fluent English...

Parexel is seeking a Regulatory Affairs Consultant - CMC vax/bio (home or office based) in Teramo, Abruzzo, Italy. You will support worldwide post-approval regulatory activities focused on CMC for vaccines or biological products and collaborate across manufacturing, QA, QC, and regulatory groups to ensure compliant submissions.You will manage regulatory...

Parexel is seeking a Regulatory Affairs Consultant - CMC vax/bio in Caserta, Italy, offering home or office based work. You will support worldwide post-approval regulatory activities focused on CMC for vaccines or biological products within a regulatory team.You will collaborate across manufacturing, QA, QC, and regulatory groups to ensure compliant...

Parexel is hiring two experienced CRAs at the CRA II or Senior CRA level to join a large Sponsor in the EU. The role encompasses site management, site monitoring and trial close-out to ensure patient safety and high-quality study execution.Key responsibilities include monitoring according to the study plan, coordinating activities across the study team and...

Parexel is seeking an Regulatory Affairs Consultant - CMC for post-approval activities related to vaccines or biological products. The role collaborates across manufacturing, QA, QC, and regulatory groups to ensure compliant submissions and timely regulatory outcomes.You will support worldwide regulatory activities, manage regulatory information systems, and...

Parexel seeks a Regulatory Affairs Consultant - CMC vax/bio to support worldwide post-approval regulatory activities focused on CMC for vaccines or biological products. You will work within a regulatory team to shape submission strategies, assess quality-related changes, and coordinate cross-functional input for regulatory dossiers.The role emphasizes...

In this role you will support worldwide post-approval regulatory activities focused on CMC for vaccines or biological products. You will work within a regulatory team to shape submission strategies, assess quality-related changes, and coordinate cross-functional input for regulatory dossiers. The position emphasizes collaboration across manufacturing, QA,...

In this role you will support worldwide post-approval regulatory activities focused on CMC for vaccines or biological products. You will work within a regulatory team to shape submission strategies, assess quality-related changes, and coordinate cross-functional input for regulatory dossiers. The position emphasizes collaboration across manufacturing, QA,...

In this role you will support worldwide post-approval regulatory activities focused on CMC for vaccines or biological products. You will work within a regulatory team to shape submission strategies, assess quality-related changes, and coordinate cross-functional input for regulatory dossiers. The position emphasizes collaboration across manufacturing, QA,...

In this role you will support worldwide post-approval regulatory activities focused on CMC for vaccines or biological products. You will work within a regulatory team to shape submission strategies, assess quality-related changes, and coordinate cross-functional input for regulatory dossiers. The position emphasizes collaboration across manufacturing, QA,...

Parexel FSP is hiring for two experienced CRA's 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 monitoring and close-out of assigned clinical trials investigator sites to ensure patient safety and quality study executionSome Specifics About This Advertised RoleEnsure...

Parexel International is seeking a Regulatory Affairs Consultant to lead post-approval activities focused on CMC for vaccines or biologics. The role allows office or home-based work across Europe.You will develop submission strategies, assess change controls, coordinate cross-department submissions, and manage information management systems. Fluent English...

About the Role We are seeking an experienced Regulatory Affairs professional to lead medical devices and combination products regulatory strategy. In this pivotal role, you will provide expert guidance on regulatory pathways for clinical investigations and marketing authorizations, and serve as the key regulatory representative for our global project...

Parexel International is seeking a Regulatory Affairs Consultant to lead post-approval activities focused on CMC for vaccines or biologics.È il candidato/la candidata ideale per questa opportunità? Lo scopra leggendo la panoramica del ruolo qui sotto.The role allows office or home-based work across Europe.You will develop submission strategies, assess...

As a Clinical Project Leader, you guide global clinical studies for Parexel's Large Pharma partners, translating clinical research experience into practical project solutions. You will lead cross-functional teams to deliver trials on time, on budget, and to the highest quality, while ensuring ICH GCP compliance and strong client satisfaction. The role...

Parexel International is seeking a Regulatory Affairs Consultant to lead post-approval activities focused on CMC for vaccines or biologics. The role allows office or home-based work across Europe. You will develop submission strategies, assess change controls, coordinate cross-department submissions, and manage information management systems. Fluent English...

Parexel International is seeking a Regulatory Affairs Consultant to lead post-approval activities focused on CMC for vaccines or biologics. The role allows office or home-based work across Europe.You will develop submission strategies, assess change controls, coordinate cross-department submissions, and manage information management systems. Fluent English...

When our values align, there's no limit to what we can achieve. At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do.Each of us, no matter what we do at...

Parexel is seeking an Regulatory Affairs Consultant - CMC for post-approval activities related to vaccines or biological products. The role collaborates across manufacturing, QA, QC, and regulatory groups to ensure compliant submissions and timely regulatory outcomes.You will support worldwide regulatory activities, manage regulatory information systems, and...