Novartis

What you’ll bring to the role: Bachelor’s degree in pharmacy / Life Sciences VBA and MS-Access knowledge will be an added advantage Advanced expertise in BI tools like Qlik/ /Alteryx/SQL Hands-on experience with the following: Qlik Sense development, data visualization, data modelling In-depth understanding of Pharma databases Earlier experience on Pharma/ healthcare could be beneficia

To be responsible for one category in one country and support the implementation of Category Strategy and Annual Category Plan, deliver projects and initiatives, and execute Supplier Performance and Innovation; to support the Category leadership with the day-to-day activities of Category management. Support the development of the Category Strategy and the Annual Category Plan, as required by the G

Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve. What you’ll bring to the role: Bachelor’s degree in pharmacy / Life Sciences VBA and MS-Access knowledge will be an added advantage Advanced expertise in BI tools like Qlik/ /Alteryx/SQL Hands-on experience with the following: Qlik Sense de

Position Purpose- Responsible for ensuring a timely implementation of all Life Cycle projects as launches/ changes/ transfers/divestment by coordination of involved partners from different functions. Ensures compliance with Regulatory and GMP, law, SOPs, HSE and Code of conduct Delivers and maintains a detailed Change Over Plan (COP) for LC projects regarding implementation dates, according to t

Help perform data analysis, identifies business needs, defines requirements, documents processes and procedures Collaborate with Health Data Insights, Transformative Design teams with a user and product-oriented mindset Gather and analyze large datasets, identify key analytical opportunities and models. Transform raw data into impactful business insights, develop and optimize the data extract

Own and drive Solution Design for Python and R Environments as part of Statistical Work Bench through addressing all business requirements and opportunities while following Novartis architectural standards, quality and information security principles Ability to get involved with engineering and/or development activities to ensure timely delivery of objectives. Participate in all Subject matter

Own and drive Solution Design for Statistical Work Bench through addressing all business requirements and opportunities while following Novartis architectural standards, quality and information security principles Prepare and run design workshops in the assigned “Products”, identify critical integration points and dependencies, propose solutions for key gaps, provide effort estimations while ensu

Design, plan and perform scientific experiments for projects at different clinical phases of drug substance and drug product with minimal guidance. Well versed with regulatory guidelines, scientific literature, technology transfer and interpretation of the results to draw conclusions in reports. Adhere to Quality metrics, Compliance and Good Documentation Practices following ALCOA+ principles, GL

To author, review and independently manage high quality clinical documents: Clinical Study Reports (CSR) including narratives, Protocol, Informed Consent Form (ICF). To write CTD modules and other safety documents (DSURs, RMPs) independently. Liaise with medical/clinical experts, statisticians, investigators in concept development when protocol is being developed and work in a collaborative fashi

Provide rotating support to the TAs according to the needs for delivery activities, i.e. co-authoring safety documents and assisting in providing safety input to regulatory and clinical documents, as well as ad hoc Health Authority queries. Assist the TA Safety Leads in monitoring the safety profile of products including with activities such as literature review, medical review/evaluation of ind