Ann: Illuccix European Marketing Authorisation Application Update, page-28

https://www.linkedin.com/jobs/view/3625912321/

Pharmacoviligance Scientist, Liège

We are seeking a motivated Pharmacovigilance Scientist to join our team and support our growth.

You will support the clinical trial program and post-market expansion in EU & UK as well as ongoing PV activities and supporting Medical Information operations

Key Responsibilities:

Manage Telix clinical trial programme's Clinical Safety activities, including SAE handling, database entry, narrative writing, and MedDRA coding.

Support post market aggregate report activities and ensure submission compliance.Handle medical information requests, tracking, and assignment.

Assist EU and UK QPPVs in maintaining essential documentation.

Maintain departmental quality documentation and provide training on safety reporting and medical information requests.

Education And Experience

You have 2 to 4 years' experience as PV,

You have case processing experience in PM and CT setting essential,

Already aggregate report writing, safety agreements and working with vendors would be considered as an asset

Working experience or knowledge of medical information activities would also be an asset

Fluent in English

Ability and willingness to work collaboratively with global team members across multiple time zones