Camila Menezes

Experience

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  CpClin - Centro de Pesquisa Clínica

  Jan 2015 - Feb 2016

  Clinical Research Trainee

  -Reading of protocols;-Training;-Development of medical records templates- Checking ICF, laboratory tests and medical records;-Organization/Registration and control of the subjects;- Send data from the source document to the sponsor by filling CRF (Case Report Form)-Registration of participants in the Interactive Web Response System (IWRS) for dispensing medication;-Solicitation, receiving, accounting, research product/research supplies;-Preparation of documentation and records for the monitoring visits and follow-up of the monitoring visits;- Check protocol deviations, pending and queries;- Performing electrocardiograms in the participants of the research;-Registration of Serious Adverse Events based on Source Documents;- Document file;-Dispensation of supplies to patients (medications, reactive tapes, journals and the like);-Realization of questionnaires with research participants according to each protocol;-Review of glycemic journals required by certain protocols and journals where the participants recorded doses and times of administration of the research product;- Follow-up visit of initiation and final visit of protocols. Show less

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  A.C.Camargo Cancer Center

  Feb 2016 - Mar 2017

  Clinical Research Assistant

  Responsible for the conduct of different clinical protocols in oncology branch, participation in medical consultations, monitoring visits, initiation visits and closure of studies. Preparation of submission documents in Plataforma Brasil and responsible for the shipment of biological samples to the central laboratory.

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  Medcin Instituto da Pele Ltda.

  Jun 2017 - now

  Clinical Research Analyst

  Commercial technical analyst, being the first contact of the sponsors with the company. Performance the designs of clinical research projects in the dermocosmetic area, ethical dossier check and all necessary documentation for conducting studies, financial and strategic planning, schedules, samples / investigational products. Follow-up and management of clinical studies that initiates the request of the proposal by the sponsors to the delivery of the final Reports, as well as the intermediary between the site to sponsor. Show less