• Submission of AE reports;• Conducting contact with AEs reporters for the purpose of elucidating information and follow-up cases;• Maintain a database of AEs received according to the product and documents related to the safety of the company's products, in a traceable way, to meet ANVISA requirements;• Reconciliation of AEs with trading partners;• Assistance in the preparation and application of training in Pharmacovigilance and Medical Information for all employees of the company and for third parties involved in the potential receipt of safety information;• Evaluation of package inserts according to CCDS, with mapping of necessary safety changes;• Elaboration, review and maintenance of standard operating procedures (SOPs) according to local and international needs;• Search for scientific articles/literature related to the company's products and projects;• Assistance in the preparation of mini-leaflets for the dissemination of promotional material with a summary of relevant scientific information about the products;• Assistance in responding to requests from external clients regarding Medical Information;• Submission of monthly Pharmacovigilance report and Medical Information metrics to Global;• Assistance in meeting requests from internal customers regarding scientific information for the preparation of promotional material;• Periodic verification of relevant safety information posted on ANVISA's website;• Execution of processes related to Pharmacovigilance with ANVISA, Global and partners;

• Provides administrative and technical support to COPM(s) and CRA(s) in daily study related tasks;• Preparation of documents for submissions to CEP/CONEP system, respecting timing for submissions, contracts and documents of the study;• Follow-up of regulatory submissions/notifications through contact with sites;• Perform activities related to study set-up, conduct, and clousure phases, in the country;• Contribute to studies site assessment in the country;• Collects and file documents, in collaboration to project team, for the Sponsor Study File (SSF), during the course of the study;• Prepare and support also the Investigator’s Study File (ISF);• Provides support to local team on TUs, lab kits and other materials to be imported to studies. Also guarantee center re-supply of TUs, lab kits and other study material;• Enter data in various computer systems (eg. TRACKIT, SETHI, SCW, WEBCTA, eTMF, eCRF, TMMCS) according to team's needs;• Plan and organize study meetings;• Support in in-house monitoring activities;• Translation and adaptation of technical documents; • Collaborate with Pharmacovigilance aspects in accordance with PV policy/procedures.

Quality in CTs activities:• Analysis of clinical trials deviations and CAPA follow-up;• Monitoring of distribution of internal procedures;• Training organization: assignments of initial and continuous trainings throught an eletronic platform, preparation and archiving of attendance sheets and certificates;• International contact with Clinical Study Support Manager (CSSM) to help in specific QA demands.Pharmacovigilance & Medical Information activities:• Receipt and processing of Pharmacovigilance, Cosmetovigilance and Medical Information cases, including contact with patients and HCPs.• Follow-up of Pharmacovigilance and Cosmetovigilance cases.• Experience with ARGUS Safety, Music, MIC/Salesforce, VigiMed, VeevaVault and MedDRA platforms.• Support in the notification of adverse events to Anvisa - clinical studies and marketed drugs.• Support in the submission of documents to investigators (clinical studies).• Assistance in PV and Medical Information trainings.• Participation in reconciliation processes.

• Receipt and processing of Pharmacovigilance, Cosmetovigilance and Medical Information cases, including contact with patients and HCPs.• Follow-up of Pharmacovigilance and Cosmetovigilance cases.• Experience with ARGUS Safety, Music, MIC/Salesforce, VigiMed, VeevaVault and MedDRA platforms.• Support in the notification of adverse events to Anvisa - clinical studies and marketed drugs.• Support in the submission of documents to investigators (clinical studies).• Assistance in PV and Medical Information trainings.• Participation in reconciliation processes.

• Support for students with content-related questions.• Assistance in the correction of academic activities.• Active participation in the weekly forums of the discipline.• Assistance in the production and/or dissemination of support material.

• Development of the project “Investigation of the involvement of the tumor microenvironment in glioblastoma proliferation”.• Experience with in vitro and in vivo models.• Performing stereotactic surgeries, Western Blotting, immunohistochemistry, histological analysis and work in a culture room.• Search for scientific articles in a database, bibliographic review and preparation of reports.• Participation in weekly article discussion meetings: presentation, interpretation and analysis of the results obtained.