David Underwood

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clinical research biometrics statistics programming medical communications clinical data management electronic data capture pharmacovigilance sas programming sdtm automation research services biostatistics contract research organization data management statistical analysis clinical trials protocol development regulatory submissions clinical study reports bayesian methods data quality oversight clinical data analysis medical writing drug development statistical programming data visualizations real world evidence pharmacokinetics pharmacodynamics rescue studies clinical trial phases cdisc mapping statistical consultancy integrated summaries adaptive trial designs randomization techniques study design data integrity risk-based monitoring interim analyses meta analysis functional service provider clinical data integration study set-up services patient monitoring clinical data quality predictive modeling study reporting pharmaceutical research sample size calculations drug efficacy therapeutic areas statistical monitoring pharmaceutical regulations outlier analysis bioavailability studies dose adjustment strategies adverse event reporting contract research organisation (cro) data analysis pharmaceutical industry biotechnology medical devices data-driven solutions patient safety risk management decentralized trials consultancy services data expertise flexible resourcing centralized data infrastructure tailored solutions client satisfaction quality standards post-marketing surveillance safety data management coding of adverse events database design cdisc compliance rapid database launch query management pharmacokinetic analysis pharmacodynamic analysis comprehensive service suite strong client relationships communication management health care health wellness & fitness hospital & health care data analytics consulting management consulting