Clinical Research Assistant

• Mar 2022 - Present

Teaching Assistant

• Aug 2015 - Present

Medical Scribe

• Jun 2020 - Feb 2022

Medical Scribe

• Jun 2014 - Mar 2020

Tutor

• Nov 2014 - Dec 2016

Sales Associate

• May 2013 - Feb 2015

Clinical Research Assistant

• Feb 2013 - Jun 2014

-Analyzed regulatory documents to verify sites followed FDA regulations and internal SOPs -Determined readiness and completeness of principle investigator files while recording deficiencies such as missing signatures, dates, PI changes, and absent ethics documents -Adequately managed and updated a formal tracking system to maintain an organized and accurate clinical database -Collaborated with In-House CRAs to ensure missing documents are retrieved within appropriate time frames… Show more -Analyzed regulatory documents to verify sites followed FDA regulations and internal SOPs -Determined readiness and completeness of principle investigator files while recording deficiencies such as missing signatures, dates, PI changes, and absent ethics documents -Adequately managed and updated a formal tracking system to maintain an organized and accurate clinical database -Collaborated with In-House CRAs to ensure missing documents are retrieved within appropriate time frames -Scanned and copied documents to ensure they were properly filed in preparation for an audit -Assisted In-House CRAs organizing and arranging packages to recruit new investigational sites -Gained familiarization with site selection, IRB submissions, study protocol, site initiation, and site management documentation Show less -Analyzed regulatory documents to verify sites followed FDA regulations and internal SOPs -Determined readiness and completeness of principle investigator files while recording deficiencies such as missing signatures, dates, PI changes, and absent ethics documents -Adequately managed and updated a formal tracking system to maintain an organized and accurate clinical database -Collaborated with In-House CRAs to ensure missing documents are retrieved within appropriate time frames… Show more -Analyzed regulatory documents to verify sites followed FDA regulations and internal SOPs -Determined readiness and completeness of principle investigator files while recording deficiencies such as missing signatures, dates, PI changes, and absent ethics documents -Adequately managed and updated a formal tracking system to maintain an organized and accurate clinical database -Collaborated with In-House CRAs to ensure missing documents are retrieved within appropriate time frames -Scanned and copied documents to ensure they were properly filed in preparation for an audit -Assisted In-House CRAs organizing and arranging packages to recruit new investigational sites -Gained familiarization with site selection, IRB submissions, study protocol, site initiation, and site management documentation Show less

Phlebotomy

• Jun 2013 - Aug 2013