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sub-investigator in a CRO or relevant academic medical center. Track record of drug submissions / approval and / or high-quality publications in international scientific journals and advanced training
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ability to collaborate with various collaborators and teams including Product, Communications, Legal, Regulatory, Compliance and International teams. • Excellent written and oral communication skills
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With nearly 50’000 patients in clinical trials at Novartis, our vision in Clinical Development is to engage these patients, making sure we have the right patients, in the right trials, at the right
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Program Team (GPT) through Life Cycle Management. • Develops and is responsible for key internal Novartis safety documents: reviews these documents regularly and updates as required (e.g. when significant
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environment, both internally and externally • Experience in leading and mentoring associates and cross-functional teams Why Novartis: Our purpose is to reimagine medicine to improve and extend people’s lives
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member of the Global Program Team (GPT), Global Clinical Team (GCT) and Clinical Trial Team (CTT) • Developing, and overall responsibility for key internal Novartis safety documents: reviewing
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• Fluent in English (oral and written), German is a plus • Excellent organizational skills, team player, flexible and dedicated personality • Demonstrated skills working in cross-functional/ international
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Team (CTT) • Developing, and overall responsibility for key internal Novartis safety documents: reviewing these documents regularly and updating as required (e.g. when significant new information is
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Infrastructure? No Offer Description We’re now accepting applications for our PhD program : unleash your potential in a vibrant, international and supportive environment. The FMI International PhD Program
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in collaboration with multi-disciplinary scientists. They must be able to communicate effectively in a highly interdisciplinary and international environment, which includes a mastery of oral and