Independent (1099) consultant involved in site selection, site initiation, monitoring and site closeout of clinical trials.
Performs and coordinates assigned aspects of the clinical monitoring process in accordance with GCPs and SOPs to assess the safety and efficacy of investigational products and/or medical devices. Conducts site visits to determine protocol and regulatory compliance, and prepares required documentation. Developed collaborative relationships with investigative sites and client company personnel.
Therapeutic Areas of CRA Research Experience:
CNS/Neurology 鈥� Epilepsy, Parkinson鈥檚 disease, Depression, Bipolar
Vaccines 鈥� Meningitis, TD, DTP Combination vaccines, Flu, Sm...
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