Business Introduction
At GSK, we have bold ambitions for patients, aiming to positively impact the health of 2.5 billion people by the end of the decade. Our R&D; focuses on discovering and delivering vaccines and medicines, combining our understanding of the immune system with cutting-edge technology to transform people’s lives. GSK fosters a culture ambitious for patients, accountable for impact, and committed to doing the right thing, making sure that we focus our efforts on accelerating significant assets that meet patients’ needs and have the highest probability of success. We’re uniting science, technology, and talent to get ahead of disease together.
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Our approach to R&D;
Position Summary
The job holder is accountable for coordinating and tracking the flow of information into the relevant Regulatory Intelligence Database (RID) and business areas and providing oversight in terms of training and communication.
Key Responsibilities
- Coordination of surveillance of GxP related regulatory intelligence with a focus on GCP related Regulatory
- Coordination of triage and liaison between different Regulatory intelligence monitors
- Assist impact assessment leads in their activities on regulatory intelligence topics
- Assist in the efforts to decommission existing tools currently supporting regulatory intelligence in exchange for the recent Freyr platform.
Coordinate tactical surveillance for RI in International on the Freyr platform and identify gaps versus current ways of working and follow up with the ARIA/Sonata team
Develop recommendations on the ways of working
Specifically, on REQUIRE assist and coordinate efforts to transition existing platform to the Freyr platform with an additional emphasis on the transformation of soft intelligence
- Assist in ensuring appropriate communication on the relevant platforms of selected regulatory intelligence topics
- Assist in ensuring proper archiving and documentation of selected impact assessments and consultati