-
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
-
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
-
. 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
-
. 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
-
analyses before internal and external (including Regulatory Authority) audiences. Language skills: High fluency in written English and strong functional fluency in spoken English. Personal skills: Strong
-
deal with a large volume of requests / deliverables on a regular basis. Ability to quickly/effectively prioritize and balance competing tasks in real-time. Demonstrated ability to flex language and style
-
correlational rules between heterogenous data sources for effective analytics and reporting Successfully bridge engineering and business with ability to speak the common language of both Provide coverage on ad
-
studies, insights, the Clinical Development Plan and regulatory strategy to ensure teams use accurate, consistent language and referencing aligned with the overarching MST strategy. Ensure the product-level