Experience

Reid Memorial Presbyterian Church
• Religious Institutions
• 1 - 100 Employee
• Preschool Teacher

  • Aug 2015 - Present

Clinical Research Advantage
• United States
• Research Services
• 1 - 100 Employee
• Clinical Reserach Coordinator

  • Jan 2013 - Mar 2014


Radiant Research

• United States
• Research Services
• 1 - 100 Employee

• Clinical Research Coordinator

  • Jan 2011 - Mar 2014

  oMaintains a high level of knowledge and understanding of assigned protocols, including all protocol requirements for patient visits, obtaining informed consent, patient visit schedules, tests, procedures, laboratory information, and drug accountability requirements oResponsible for completion of all study documentation forms, including case report forms and other study specific documents oCoordinates and conducts patient care visits and assures all procedures are conducted in compliance with the clinical protocol oInteracts with Principal Investigator as needed to assure patient receives appropriate medical evaluation and care when needed; alerts Principal Investigator of serious adverse events oInteracts with sponser Clinical Research Associate to facilitate the sponsor monitoring and database clean-up process oAttends sponsor Investigator/Study Coordinator meetings as needed for assigned protocols oConducts clinical research in compliance with all applicable regulations Show less



Millennium Therapeutics and Research, LLC

• Clinical Research Coordinator

  • Mar 2010 - Jan 2011

  o Clinical Research Coordinator duties include but are not limited to: screening subjects, enrolling subjects in clinical trials, careful explanation and teaching of Informed Consent process, completion of pertinent documents, maintaining source documentation and regulatory binders, tracking adverse events. o Administering investigational product, collection, processing, and shipping of biological specimens, ECG procedure, maintain correspondence between Principal Investigator and research facilitator. o Executing study procedures according to protocol, generation and completion of source documents, completion of case report forms, in depth understanding and adherence to ICH/FDA/ Good Clinical Practices, clinical trial/time management and regulatory compliance in relation to clinical research, QC auditing for sister sites, SAE/deviation auditing and tracking, staff training on protocol and procedures. o Query resolution and extensive experience with RDC/EDC data entry sites. o Extensive use of Microsoft and Excel computer programming, email correspondence and participation in professional continuing education, investigator meeting attendance, and provider of assistance to other sites for new coordinator training; expense reports and related documentation Show less



Kidney Care Associates

• United States
• 1 - 100 Employee

• Clinical Research Coordinator

  • 2005 - 2009

  o Assistant Clinical Research Coordinator for the dialysis arm of the organization. o Duties include: enrolling subjects in clinical trial, maintaining source documentation, and regulatory binder, administering investigational product, tracking adverse events, and query resolution. o Collection, processing, and shipping of biological specimens, ECG procedure, maintaining correspondence between Principle Investigator and research facilitator. o Researched and produced informational brochures for patient educationo Research Assistant while functioning at the level of a clinical research coordinator. o Chart review for study screening, data entry, maintaining source documentation, processing and shipping of biological specimens o Patient interaction, preparation, and education. Show less


Meco Inc
• Industrial Machinery Manufacturing
• 1 - 100 Employee
• clerk

  • 2000 - 2005