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skills. Strong oral presentation skills, including ability to present and explain data analyses. Language skills. High fluency in spoken and written English. Knowledge of how to use publicly available
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following levels of education/experience: BS/BSc/MS/MSc or equivalent + 7 years of clinical research experience and/or quality management experience. Skills in more than one language are an advantage in
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) Proficiency in local language preferred. English is required. Demonstrated experience in site management with prior experience as a site monitor Demonstrated experience in start up activities through to site
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of education/experience: BS/BSc/MS/MSc or equivalent + 7 years of clinical research experience and/or quality management experience. Skills in more than one language are an advantage in this role. English is
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regulations Understanding of Network/Server/Virtualization best practices Understanding of software/document repositories/versioning Understanding of programming, and proficiency in at least one language
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or equivalent with 7+ years of clinical research experience and/or quality management experience. Skills in more than one language are an advantage in this role. English is required. Experience with drug
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regulations Understanding of Network/Server/Virtualization best practices Understanding of software/document repositories/versioning Understanding of programming, and proficiency in at least one language
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regulations. Understanding of Network/Server/Virtualization best practices. Understanding of software/document repositories/versioning. Understanding of programming, and proficiency in at least one language
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and training abilities. Nice to Have DeltaV and/or PLC experience. Understanding of programming, and proficiency in at least one language. Direct knowledge and experience in automation qualification
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, and proficiency in at least one language. Direct knowledge and experience in automation qualification or verification within a biopharmaceutical or pharmaceutical cGMP environment is desired. Experience