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cutting edge design and process development capabilities to accelerate and bring the best in class medicines to patients around the world. ROLE SUMMARY This position will provide statistical support for
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, external alliances or committees, consortia and academic relationships. BASIC QUALIFICATIONS PhD in Pharmacometrics, Clinical Pharmacology, Pharmacokinetics, Engineering, Pharmaceutical Sciences, Statistics
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statistics. You should be highly motivated; should possess excellent written and verbal communication skills; and should be able to effectively collaborate with different functional groups (e.g., Statistics
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clinical findings from statistical noise is a non-trivial task. A successful applicant will leverage modern data-science and bioinformatics approaches to explore high dimensional datasets, such as multiomic
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(director/Sr director) provides clinical input to protocol/study team for monitoring guidelines, statistics analysis plans, ICDs, clinical review forms, data edit checks, data quality planning, as needed
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Strong quantitative modeling skills (e.g., pharmacometrics, pharmacokinetics, mechanistic modeling/systems pharmacology, statistics). Experience with R software Strong communication skills--written, oral
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to protocol/study team for monitoring guidelines, statistics analysis plans, ICDs, clinical review forms, data edit checks, data quality planning, as needed (ultimately oversees work of protocol/study team
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and scale up of API manufacturing processes. You will design and perform engineering-related laboratory experiments , in combination with process simulation and statistics. Strong communication , high
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as a resource to consult with project statisticians and statistics heads in establishing consistent global systems and processes. Support planning, delivery, and communication of statistical analyses
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, principles and statistical aspects of advanced mathematical modeling and simulation Ability to effectively translate/condense/summarize outcomes of modeling and simulation analyses into useable information