Hours of work

Mon - Fri (35 hours a week)

Onsite requirement

This will be a hybrid role, with 3 days per week on site.

Location

West London, England

Job Purpose

To support management of Patient Safety operational processes at Country Organization ensuring compliance with global and local procedures, national and international regulations/ standards/ guidelines for vigilance of both marketed and investigational products (incl. drugs, food supplements and medical devices).

Major Accountabilities

• Manage the collection, processing, documentation, reporting and follow-up of all adverse event reports for products from Clinical Trials, Non-interventional Studies, Patient Oriented Program (POPs), Literature, Spontaneous Reports, and any other source of information.
• Liaise with the External Service Provider for case processing to ensure compliance with Procedures.
• Develop, update, a...