Novartis Jobs in London
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Novartis Farmacéutica-London
management, and regulatory requirements for clinical studies designated for review by regulatory authorities.
Why Novartis: Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people...
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Novartis Farmacéutica-London
for internal customers/stakeholders, e.g., GMA supportive functions (Real World Evidence, SciComms, Field Medical), Clinical, Biomedical Research, Marketing, Novartis local medical organizations, as well as external customers e.g. medical experts (MEs...
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Novartis Farmacéutica-London
and quality by fostering statistical programming innovations, processes and solutions that ensure efficient implementation and knowledge sharing across Novartis.
• You will be required to drive productivity and efficiency measures to meet the strategic...
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Novartis-London
quality and/or clinical development.
Why Novartis:
Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining...
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Novartis Farmacéutica-London
Biomedical Research, Marketing, Novartis local medical organizations, as well as external customers e.g. medical experts (MEs), healthcare system stakeholders and patient advocacy groups.
• For assigned Medical Affairs studies (Phase IIIB-IV without...
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Novartis Farmacéutica-London
Firm working knowledge of GCP, scientific and clinical methodology, protocol designs, management, and regulatory requirements for clinical studies designated for review by regulatory authorities.
Why Novartis: Helping people with disease...
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Novartis-London
of product development.
4. Ability to work independently and in a global/matrix environment.
5. 3 or more years experience in managing projects.
6. Strong skills in GCP, quality and/or clinical development.
Why Novartis:
Helping people with disease...
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Novartis Farmacéutica-London
generation.
• Ensures compliance with applicable US and international Medical Device regulations and standards including, but not limited to, 21 CFR 820, ISO 13485, 93/42/EEC, 98/79 EC, and the requirements of the Novartis CDx Quality Management System...
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Novartis Farmacéutica-London
in performance management and talent planning processes. Provide on-boarding, training, & mentoring support
• Contribute to medical/scientific training of relevant Novartis stakeholders on the disease area and compound/molecule. May serve as speaker for franchise...
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Novartis Farmacéutica-London
leader in drug development biostatistics across related indications/areas within Novartis and across the external scientific/research community
Key requirements:
• Ensure expert level contribution to strategy (design, analysis/synthesis, interpretation...
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Novartis Farmacéutica-London
of in-licensing opportunities.
• Fosters and develops new quantitative methods with the aim of improving drug development at Novartis in multiple projects. The focus includes clinical trial design, modeling, visualization and machine learning
• Actively evaluates...
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Novartis Farmacéutica-London
and standards including, but not limited to, 21 CFR 820, ISO 13485, 93/42/EEC, 98/79 EC, and the requirements of the Novartis CDx Quality Management System.
Education: MD or Ph.D. OR MD/Ph.D. with minimum of 6 years of experience in the field of precision...
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Novartis Farmacéutica-London
US and international Medical Device regulations and standards including, but not limited to, 21 CFR 820, ISO 13485, 93/42/EEC, 98/79 EC, and the requirements of the Novartis CDx Quality Management System.
10. 6 years industry experience.
11. 3...
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Novartis Farmacéutica-London
development.
• Ability to manage parallel multiple projects in different therapeutic areas.
Why Novartis: Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you...
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Novartis-London
Research, Marketing, Novartis local medical organizations, as well as external customers e.g. medical experts (MEs), healthcare system stakeholders and patient advocacy groups.
• For assigned Medical Affairs studies (Phase IIIB-IV without regulatory impact...
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