Fernanda Munari Email & Phone Number
Who is Fernanda Munari? Overview
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Fernanda Munari is listed as DTI-A Researcher at Hospital de Amor, a with 454 employees, based in Barretos, São Paulo, Brazil. AeroLeads shows a matched LinkedIn profile for Fernanda Munari.
Fernanda Munari previously worked as DTI-B Researcher at Hospital De Amor and Clinical Study Coordinator at Hospital De Amor Barretos. Fernanda Munari holds Pesquisa Clínica, Clinical Research Coordinator from Uninter Centro Universitário Internacional.
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About Fernanda Munari
Fernanda Munari is a DTI-A Researcher at Hospital de Amor. She possess expertise in biologia molecular, pesquisa, entrada de dados, pcr, sequenciamento de dna. She is proficient in Espanhol and Inglês. Colleagues describe her as "Profissional comprometida que tenho muito prazer em poder compartilhar e viver experiencias diárias na condução de estudos clínicos. Profissional extremamente aberta para conversa e discussão de diversos aspectos de nosso dia a dia. Sempre muito disposta a ouvir, dividir e compartilhar todo conhecimento envolvido em nossa área de atuação. Você agrega muito em nosso grupo de coordenadores!!" and "Profissional super competente em pesquisa clínica!!! Muito atenciosa e dedicada em sua área. "
Listed skills include Biologia Molecular, Pesquisa, Entrada De Dados, Pcr, and 1 others.
Fernanda Munari's current company
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Fernanda Munari work experience
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Clinical Study Coordinator
• Conducting phase I, II, III clinical trials.• Conducting of clinical trial of covid-19 vaccine.• Compliance with Good Clinical Practices (GCP) of the conducted clinical trials.• Conducting SIVs (Initiation Visit), COV (Closet-out Visit) and monitoring visits.• Assistance in the development of SOP (Standard Operating Procedure).• Application of the Informed Consent Form.• Clinical data from medical records collection.• Insert data entry into eCRF.• Experience with IWRS.• Completion and monitoring of documentation in accordance with local regulatory requirements and deadlines requested by the sponsor, ensuring data quality.• Enable research assistants and interns, with ongoing guidance/training, for professional and departmental development.• Apply corrective or preventive measures resulting from monitoring and audit visits by sponsors, aiming at compliance with agreed procedures.• Monitor the treatment of each participant, ensuring that the stages of the study are being strictly followed.• Carry out the proper processing and shipping of biological samples according to the requirements of each protocol.• Carry out submissions to the CEP/CONEP platforms of research protocols, as well as deviations, half-yearly reports and SAE.
Project Coordinator
Department: Researcher Support Center (NAP)Responsibilities: • Conducting of clinical studies in oncology.• Compliance with Good Clinical Practices (GCP) of the conducted projects.• Application of the Informed Consent Form.• Clinical data from medical records collection.• Insert data entry into eCRF.• Submission in the CEP/CONEP system.• Making the study binders.• Biological material collection.• Managing patients through a database on the REDCap platform.• Completion and monitoring of documentation in accordance with local regulatory requirements and deadlines requested by the sponsor, ensuring data quality.• Presentation and feedback on the progress of studies to the sponsor and principal investigator (PI).• Carry out the storage/handling and replacement of materials from the studies conducted by the department according to established procedures.• Enable research assistants and interns, with ongoing guidance/training, for professional and departmental development.• Developing tools that facilitate work routines.• Orientation of the Course Completion Work for nursing residency students.• Organization of the Symposium on Bioethics and Clinical Research.• Participation as coordinator on duty in the study of the COVID-19 vaccine in the Clinical Research Unit.
Biologist L
Department: Molecular Oncology Research Center and Pathology.Responsibilities: • Compliance with Good Clinical Practices (GCP) and Good Laboratory Practices of the conducted projects.• Conducting oncology studies experiments.• Survey, control and purchase of inputs for the studies.• Data collection and analysis.• Clinical data from medical records collection• Completion and correct monitoring of data in eCRF.• Biological material collection.• Application of the Informed Consent Form.• Carrying out laboratory experiments of the studies: DNA/RNA extraction, PCR, Real-Time, Sanger sequencing, next generation sequencing (NGS), histological sections, immunohistochemistry, COBAS (HPV genotyping).• Presentation and feedback on the progress of studies to the sponsor and principal investigator (PI).• Written development of scientific articles for publication in international journals.
Graduate Scholarship (Master Degree)
Master's level scholarship sponsored by FAPESP.Department: Molecular Oncology Research Center.Responsibilities:• Development of scientific experiments.• Survey, control and purchase of inputs for the study.• Enter data entry into eCRF.• Data collection and analysis.• Collection and storage of biological material.• Application of the Informed Consent Form.• Performing all experiments: DNA extraction, PCR, Sanger sequencing, next generation sequencing (NGS), and HPV genotyping using Luminex techniques.• Conducting the collection of sociodemographic information from research participants, by reading and searching for information in the literature about the study conducted.
Professor
Professor in the disciplines of TCC, Basic Immunology, Microbiology and Patient Safety.
Visiting Researcher
• Development an observational study related to esophageal cancer;• Interpretation of esophageal tumor bioinformatics data;• Preparation of scientific report;• Presentations of scientific articles at group meetings;• Development and interpretation of bioinformatics data from cases of esophageal tumors for writing the scientific article and reports;• Course and training in Introduction to Biological data analysis with R.
Fernanda Munari education
Pesquisa Clínica, Clinical Research Coordinator
Master'S Degree, Health Sciences (Molecular Oncology)
Postgraduate Degree, Molecular Biology And Genetics In Health Sciences
Bachelor'S Degree, Biological Sciences
Frequently asked questions about Fernanda Munari
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What company does Fernanda Munari work for?
Fernanda Munari works for Hospital de Amor.
What is Fernanda Munari's role at Hospital de Amor?
Fernanda Munari is listed as DTI-A Researcher at Hospital de Amor.
Where is Fernanda Munari based?
Fernanda Munari is based in Barretos, São Paulo, Brazil while working with Hospital de Amor.
What companies has Fernanda Munari worked for?
Fernanda Munari has worked for Hospital De Amor, Hospital De Amor Barretos, Liceutec Barretos, and I3S - Instituto De Investigação E Inovação Em Saúde.
How can I contact Fernanda Munari?
You can use AeroLeads to view verified contact signals for Fernanda Munari at Hospital de Amor, including work email, phone, and LinkedIn data when available.
What schools did Fernanda Munari attend?
Fernanda Munari holds Pesquisa Clínica, Clinical Research Coordinator from Uninter Centro Universitário Internacional.
What skills is Fernanda Munari known for?
Fernanda Munari is listed with skills including Biologia Molecular, Pesquisa, Entrada De Dados, Pcr, and Sequenciamento De Dna.
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