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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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equipment. Strong knowledge of Computerized Systems, Compliance regulations and standards. Understanding of programming, and proficiency in at least one language. Teamwork spirit, good communication skills
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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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automated systems Knowledge of Sharepoint, Spotfire and other applications for equipment scheduling, issue tracking and performance visualizations Some experience in coding in Python or other 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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medical communications and understanding of applicable regional legal and regulatory hurdles. Experience with omnichannel, including diverse content development - such as publications, plain language
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antibody API materials for clinical (including late stage clinical) and cGMP commercial phases. Understanding of programming, and proficiency in at least one language. PHYSICAL/MENTAL REQUIREMENTS Physical
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degree with 0+ years of experience. Familiar with process controls equipment. Understanding of programming, and proficiency in at least one language. Knowledge of Computerized Systems. Teamwork spirit
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. Proficiency in integration of molecular profiling data including transcriptomic, proteomic, and genomic datasets. Experience using R-programing language for interpretation of large multi-omic data sets
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. Oral presentation skills: Strong oral presentation skills, including ability to present, explain and defend data analyses before internal and external (including Regulatory Authority) audiences. Language