...of the company, it’s growth, innovation, culture and how Sandoz impacts the lives of... ...Responsible for improvement for Life Cycle Management of the Business System/App...
About the Role
Job Purpose
In close collaboration with the Global Program Safety Lead (GPSL) provides robust safety evaluation expertise and medical innovation in order to improve patients’ lives and impact on overall Novartis results. As a mem...
About the role
Millions! Novartis made a decision to pursue early discovery research internally to allow us to quickly translate the most impactful discoveries into therapeutics for millions of patients. With the ever-evolving global regulations ...
...About the role
Collaborates with Director ESP Engagement to ensure Governance, Contracts and Transitions of Global External Service Providers. In addition, support Director ESP Engagement to develop, communicate ...
About the Role
“150! Clinical scientific experts, globally, are part of Global Drug Development (GDD) team, working to ensure clinical trial data and regulatory reports are of highest quality throughout the life cycle of each program, across all di...
About the Role
Job Purpose
Acts as Manager Systems Operations working and supporting Managers/Experts System Operations. Responsible for working with internal and external partners to implement cross-functional processes, technologies, solution...
At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide ...
About the Role
This role combines responsibilities in Medical Safety Operations (addressing pharmacovigilance (PV) needs) with broad Project Management activities. Reporting to the Head Medical Safety (MS) Processes & Pro...
Performs day-to-day PV activities. May participate in on-call duties for specific projects to ensure 24-hr coverage for intake of cases from investigative sites.
Reviews regulatory/pharmacovigilance publications and information sources to keep ...
About the role
“150! Clinical scientific experts, globally, are part of Global Drug Development (GDD) team, working to ensure clinical trial data and regulatory reports are of highest quality throughout the life cycle of each program, across all d...
