- Conduct pre-study, initiation, interim and close-out monitoring visits for phase III trials according to GCP and Targetís SOPs.
- Prepare reports on study status and monitoring activity
- Assist with tracking of pre-study documents, as required; assist with tracking of documents during the course of the study
- Responsible for the set-up and maintenance of the Study Master Files that include both paper and electronic files
- Prepare, distribute and track study center start-up materials and documents that include confidentiality agreements (CDAs) and site agreements (CSAs), and all regulatory documents
- Obtain, document and track IRB documentation, investigator and clinical laboratory license expiration dates and track receipt of clinical supplies at study sites

- Isolate and characterize products using various chromatographic and spectroscopic techniques such as: thin-layer chromatography, flash chromatography, FT-IR and NMR
- Conduct reactivity studies using isolated products and analyze results in order to determine effects on asymmetric oxidation reactions

- Assist professors in the preparation, demonstration and troubleshooting of experiments in general and inorganic laboratories
- Instruct students on the appropriate operation of instrumentation and provide any needed assistance with bench top techniques
- Grade lab reports and assist professor in the evaluation of student performance

Currently working on a Master of Science degree in Inorganic Chemistry with classes taken in Medicinal Chemistry, Organic Chemistry and Analytical Chemistry

Bachelor of Science in Chemistry

High School