...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...
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Job Purpose
To provide quantitative analytical support for PS&PV by ensuring timely delivery of high quality reports to meet regulatory requirements, enable medical safety analysis and monitor safety profile of Novartis products...
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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 ...
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PK Sciences (PKS) offers you this opportunity to make an impact, where 450 projects are straddling discovery through development. PKS is a global organization of about 300 associates, situated within Translational Medicine (TM), in...
...About the role
Senior Medical Information Manager I
Location – Hyderabad #LI Hybrid
About the Role:
To be responsible for delivering sophisticated and highly sophisticated Medical Information (MI) activi...
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Design, plan, perform, interpret and report results of scientific experiments for the preparation and timely delivery of analytical methods for drug products (DP), processes and procedures. Lead and manage all project/local network...
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Location: Hyderabad
Role: Associate Director, GDD Data Team
Function & Responsibilities: Development Data Team is responsible to design and execute data management strategy across Drug Development line functions i.e. Clinical ...
About the Role
Location: Hyderabad
Role: Associate Director, GDD Data Team
Function & Responsibilities: Development Data Team is... ...collaborates with cross domains such as Technical Operat...
About the role
200! This is the number of experimental data generated every single day in the Pharmacokinetic Sciences (PKS) department at Novartis Biomedical Research on drug discovery projects. We need you to extract knowledge out of these data ...
...degradation product, extractable and leachable.
3. Genotoxicity hazard assessment for impurities using in-vitro and in-vivo data and in-silico (Q)SAR approaches (according to ICH M7 guideline).
4. Determination ...
