Experience

CTI Consulting

• United States
• IT Services and IT Consulting
• 1 - 100 Employee

• Senior clinical research associate

  • Aug 2013 - Present



Premier Research

• Sr. Clinical research associate

  • 2011 - May 2013



Corza Wound Closure

• Medical Device
• 100 - 200 Employee

• Principal Clinical Research Associate 4

  • May 2005 - Feb 2011

  Monitored the conduct of multi-center Phase II study involving the Treatment of Patients undergoing Hemodialysis using an implanted graft access. • Maintain a high level of professional expertise through familiarity with clinical literature and participation in project meetings • Coordinate study management activities including regulatory document management, site selection, study start-up activities, study information tracking and site management • Monitor clinical studies and coordinate clinical activities to ensure compliance with protocol and overall clinical objectives • Liaison for all clinical study related activities • Analyze and evaluate all clinical data collected from the clinical sites to ensure complete and accurate data • Coordinate and resolve all inquiries and problems associated with clinical investigations. • Prepare clinical reports as needed for regulatory submissions and upon request when required for presentations • Assist with selection of appropriate study sites to conduct clinical studies • Assist with the training of new clinical research associates • Assist with review and development of clinical protocols and associated study documents Show less



SFBC New Drug Services

• Sr Regional Clinical Research Associate

  • Aug 2002 - Jun 2005

  Monitored the conduct of multi-center Phase II study involving the Treatment of Patients undergoing Hemodialysis using an implanted graft access. • Maintain a high level of professional expertise through familiarity with clinical literature and participation in project meetings • Coordinate study management activities including regulatory document management, site selection, study start-up activities, study information tracking and site management • Monitor clinical studies and coordinate clinical activities to ensure compliance with protocol and overall clinical objectives • Liaison for all clinical study related activities • Analyze and evaluate all clinical data collected from the clinical sites to ensure complete and accurate data • Coordinate and resolve all inquiries and problems associated with clinical investigations. • Prepare clinical reports as needed for regulatory submissions and upon request when required for presentations • Assist with selection of appropriate study sites to conduct clinical studies • Assist with the training of new clinical research associates • Assist with review and development of clinical protocols and associated study documents Show less