Under supervision gather and summarize literature on various topics as they relate to pharmacology / pharmacokinetics topics.
Can perform data entry/data cleaning activities
Can review bioanalytical reports for non-GLP/GLP/GCP studies
Can contribute to the planning and implementation of bioequivalence, pharmacokinetic, pharmacodynamic, and clinical studies adhering to Good Clinical Practices
Will be expected to contribute to reviewing study data listings, preparing study reports, preparing investigator brochures, editorial support for publications, and assisting with NDA applications
Prepare presentations on topics related to pharmacology
Good understanding of statistical concepts