Bonita began her professional career as a critical care nurse which gave her a strong clinical background. During this time, Bonita was responsible for providing care to patients in life-threatening situations. She had to make quick decisions that could mean the difference between life or death. This experience gave her a strong sense of the importance of patient safety and the need to advocate for their rights. In her role as a clinical trials auditor, she uses this understanding to ensure that the rights and wellbeing of study participants in clinical trials are protected and that their clinical data is valid and traceable. She is also highly skilled at identifying potential risks to study participant safety.
Clinical Research Experience
Bonita’s 35-year career in clinical research began in 1989 when she held the position of Cardiac Arrhythmia Research Nurse in the academic setting where she worked under the guidance of several world renown cardiac electrophysiologists that taught her the basic principles and ethical standards of clinical research in the academic setting. Over the next 10 years, Bonita moved on to the private sector and held positions as Phase I Special Populations Research Nurse, Phase I-IV Research Nurse, and Staff Development Research Nurse at a large privately owned clinical research Investigative site where she trained investigators, clinical research coordinators, research nurses, data entry personnel, laboratory and regulatory staff regarding the proper set up and operationalization of clinical research protocols at the Investigative Site. This included the creation and utilization of source documents, organization and conduct of timed study specific events, proper data collection and data entry processes, safety reporting, organization, and management of the Investigator Site File, responding to site clinical monitoring and data management queries in a timely manner, and responding to site regulatory inspections.
Bonita began her professional career as a critical care nurse which gave her a strong clinical background. During this time, Bonita was responsible for providing care to patients in life-threatening situations. She had to make quick decisions that could mean the difference between life or death. This experience gave her a strong sense of the importance of patient safety and the need to advocate for their rights. In her role as a clinical trials auditor, she uses this understanding to ensure that the rights and wellbeing of study participants in clinical trials are protected and that their clinical data is valid and traceable. She is also highly skilled at identifying potential risks to study participant safety.
Clinical Research Experience
Bonita’s 35-year career in clinical research began in 1989 when she held the position of Cardiac Arrhythmia Research Nurse in the academic setting where she worked under the guidance of several world renown cardiac electrophysiologists that taught her the basic principles and ethical standards of clinical research in the academic setting. Over the next 10 years, Bonita moved on to the private sector and held positions as Phase I Special Populations Research Nurse, Phase I-IV Research Nurse, and Staff Development Research Nurse at a large privately owned clinical research Investigative site where she trained investigators, clinical research coordinators, research nurses, data entry personnel, laboratory and regulatory staff regarding the proper set up and operationalization of clinical research protocols at the Investigative Site. This included the creation and utilization of source documents, organization and conduct of timed study specific events, proper data collection and data entry processes, safety reporting, organization, and management of the Investigator Site File, responding to site clinical monitoring and data management queries in a timely manner, and responding to site regulatory inspections.
Bonita brings years of valuable Clinical Research Quality Assurance experience to every project
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