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ViiV Healthcare is recruiting for a Director, Clinical Pharmacology Leader who will provide translational and clinical discovery and development..
Site Name: UK - London - Brentford Posted Date: Jan 7 2021 Product Tech Designer GSK House Based About GSK Pharma Tech GSK is on a mission
The primary focus of this role is to handle activities relating to: the provision of safety, risk mitigation and pharmacovigilance (PV) support
This role is to execute technical strategies in analytical chemistry, within a region or category, which is focused on the delivery of innovation
This role is to execute technical strategies in analytical chemistry within a region or category, which is focused on the delivery of innovation
We have a fantastic opportunity for a talented Global Regulatory Affairs Associate Director/ Manager with strong regulatory affairs
This is a significant role as part of the Global EHS Shared Service team for Consumer Health.
Within the Biopharm Discovery Unit, the Antibody Selections group is looking for an experienced Antibody Engineer.
This role ensures GSK's global energy and utility strategies and initiatives have the privilege of focus to ensure delivery.
This role ensures GSK's global sustainability strategies and initiatives have the privilege of focus to ensure delivery.
The role is responsible for the leadership of a team focused on defining and driving the GCI/EM regulatory policy, advocacy and intelligence
Within the clinical programming team Senior Programmers and Principal Programmers support, guide, or make a major contribution to the
The essence of the Pharmacovigilance (PV) Systems groups is to provide a channel between PV system users and IT suppliers and back again
Are you interested in a highly visible medical affairs role that allows you to shape and execute the brand medical strategy,
In this role you will lead operations for Value Evidence and Outcomes (VEO).
Ensure the development of appropriate regional regulatory strategy(s) and their execution for assigned asset(s) consistent with Medicines Development
The Global Medical Affairs Leader is accountable for Phase IV evidence generation studies, including post-approval commitments and health
Do you have excellent data skills and a passion to upskill others? Are you seeking a new challenge in leading change?
The Regulatory Project Manager is responsible for the timely production of approved documentation for clinical trials and marketing applications