Leukemia/lymphoma team: As part of the research team, I use my 3+ year of research experience and 18 years of experience working as an MD in Brazil to ensure subject safety and welfare. My duties entail ascertaining eligibility, recruiting, obtaining or verifying informed consent prior to subject participation, maintenance of study materials and database, data entry, conducting patient visits, maintaining regulatory files, and scheduling, implementing, and tracking study procedures. I maintain consistent contact with study team members to ensure successful implementation of study procedures and standards of patient care per the protocol.

As part of the research team, I use my 3+ year of research experience and 18 years of experience working as an MD in Brazil to ensure subject safety and welfare. My duties entail ascertaining eligibility, recruiting, obtaining or verifying informed consent prior to subject participation, maintenance of study materials and database, data entry, conducting patient visits, maintaining regulatory files, and scheduling, implementing, and tracking study procedures. I maintain consistent contact with study team members to ensure successful implementation of study procedures and standards of patient care per the protocol.

As part of the research team, I use my 3+year of Research experience and 18 years of experience working as an MD in Brazil to ensure subject safety and welfare. My duties entail ascertaining recruiting, eligibility, obtaining or verifying informed consent prior to subject participation, maintenance of study materials and database, data entry, conducting patient visits, maintaining regulatory files, and scheduling, implementing, and tracking study procedures. I maintain consistent contact with study team members to ensure successful implementation of study procedures and standards of patient care per the protocol.

Competencies including: ● ICH GCP E6 R (2)● FDA Regulations 21CFR 11, 50, 54, 56 and the Common Rule 45CFR46● Data Management● Informed Consent Process● Clinical Trial Operations from feasibility through close-out● GDP following ALCOA-C principles● Identification and reporting of AEs and SAEs● Quality Assurance, Monitoring and Query Resolution● Comprehension and Execution of Clinical Trial Protocols● Maintaining a regulatory binder, housing essential documents including but not limited to 1572, DOA, Training Logs and other Investigator Site File (ISF) document

• Supervised and managed research team researching Brain Death and Pediatric ER situations, assisting with data collection, data analysis, and scientific research methodology design.• Trained pediatric ER team consisting of 9 pediatricians, 15 nurses, and 19 CNAs about pediatric ER diagnoses, new treatments, and management updates.• Coordinated group that provided data about brain death, including causes and protocols, to 100 families per month in the hospital.

• Attended approximately 30 patients per month in the Pediatric Intensive Care Unit (PICU) and 129 patients per month in the ER.• Trained pediatric and PICU residents and presented scientific articles published in renowned medical journals and magazines to advance their knowledge of the latest treatments and discoveries.• Served as a Horizontal Medical Information provider, providing other physicians with the optimum information to make the best decisions and obtain the best results.

• Worked with multidisciplinary team of a dietitian, social worker, psychologist, and geneticist, collecting data, evaluating lab results, researching the best nutrition options for pediatric patients, and presenting the results at International Geneticist events.Worked in Clinical trial , GCP phase 1,2 trials.

• Provided skilled emergency care to critically ill patients, monitoring patient conditions and updating team members on changes in stability or acuity.