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Novellas Healthcare

Belgium|Pharmaceuticals|Employee

Global Clinical Trial Submission Specialist

We want you to be our new Global Clinical Trial.
Your responsibility:
Planning, coordination, preparation and tracking of the documents needed for initial submission Start-up) and Substantial amendments (ongoing) of Clinical Study package for all countries (except US) in compliance with the Country Regulatory Requirements, EU clinical Trial directive, related Guidance, and the processes.

Description

Sarah Sarah Vancutsem

Novellas Healthcare

Belgium|Pharmaceuticals|Employee

Pharmacovigilance Officer | Vlaams Brabant

For one of our clients, an independent consulting agency, founded in the early 1990s, we are searching for a Project Manager with a first experience in Pharmacovigilance.
Our client collaborates with a team of dedicated and highly trained professionals in the pharmaceutical and biomedical field.
They provide compliance solutions and consultancy services for medicinal products for human and for veterinary use, medical devices and other healthcare products.

Description

Roxane Roxane Leloup

Novellas

Belgium|Pharmaceuticals|Employee

Technical Regulatory Writer | Wavre

The Technical Regulatory Writer is involved in the company’s regulatory activities related to new & exisiting products, on a domestic or international basis. Activities focused on technical writing for US-Facilities, with focus on the New IPV building submission.

Description

Sarah Sarah Vancutsem