Experience

Faculty of Medical Sciences of Minas Gerais

• Brazil
• Higher Education
• 200 - 300 Employee

• Professor and Researcher

  • Mar 2010 - Present

  - Professor of Genetics for Medical Students; - Professor of Research Ethics for Master Degree Students; - Professor of Scientific Methodology for Nurse Students; - Professor of Pharmacology for Physiotherapy Students; - Coordinator of Lato Sensu Specialization in Clinical Research. - Professor of Genetics for Medical Students; - Professor of Research Ethics for Master Degree Students; - Professor of Scientific Methodology for Nurse Students; - Professor of Pharmacology for Physiotherapy Students; - Coordinator of Lato Sensu Specialization in Clinical Research.



Centro de Oncologia de Precisão

• Belo Horizonte, Minas Gerais, Brasil

• Senior Pharmacist

  • Feb 2020 - Dec 2021

  In charge of patients' data bank for clinical research. In charge of patients' data bank for clinical research.



Governo do Estado de Minas Gerais

• Brazil
• Public Policy Offices
• 700 & Above Employee

• Forensic Toxicologist

  • Jul 1992 - Jul 2017

  Official toxicologist at Legal Medicine Institute Official toxicologist at Legal Medicine Institute



Trymed

• Belo Horizonte e Região, Brasil

• Clinical Research Manager

  • Jan 2011 - Jan 2015

  - Managing new and ongoing clinical trials in the areas as Cardiology, Pneumology, Endocrinology, Psychiatry, and Vaccines. - Prospection of new trials with big pharma and CRO´s. - Responsible for identification and selection of new investigators and institutions for clinical trials in all therapeutic areas. - Responsible for the development of recruitment strategies to increase patient randomization into the trial. - Responsible for approval for trials from ethics committee. - Managing and training of the research coordinator team. - In charge of training other professionals, such as clinical trial investigators according to local and international guidelines. - Responsible for budget and contract analysis. - Experience of over 10 clinical trials phases III and IV. - Work with sponsor and CRO´s team to establish regulatory requirements and contracts. - Ensure clinical quality delivery by applying quality standards/requirements with close follow up based on measuring, monitoring and management of clinical quality issues. - Conduct regular team meetings to achieve objectives for trials.



Biocancer

• Belo Horizonte e Região, Brasil

• Clinical Research Manager

  • Mar 2004 - Dec 2010

  - Managing new and ongoing clinical trials in the Oncology area; - In charge of preparing protocols and case forms and finalizing pre-monitoring and data management options. - Responsible for the development of recruitment methods to increase patient randomization into the trial; - Responsible for approval for trials from ethics committee; - Managing of the research coordinator team; - In charge of training other professionals, such as clinical trial investigators, clinical trial nurses, and other clinical trial associates. - Responsible for identification and selection of new investigators and institutions for clinical trials; - Responsible for budget and contract analysis. - Experience of over 40 clinical trials from phase II to IV.