Almirane Oliveira

• Support in the collection, review, and processing of adverse event data in accordance with pharmacovigilance regulations and company procedures. • Assistance in the preparation and submission of safety reports to regulatory authorities and stakeholders. • Collaboration with cross-functional teams to ensure timely and accurate communication of safety information. • Contribution to the development and maintenance of pharmacovigilance documentation, including standard operating procedures and safety management plans.

• Clinical practice integrated within the multidisciplinary team, focused on the identification and prevention of medication-related adverse events, resulting in reduced care-related risks; • Active surveillance, validation, and reporting of Adverse Drug Reactions (ADRs) to VigiMed/ANVISA, strengthening patient safety and the quality of pharmacovigilance data; • Analysis and validation of medical prescriptions, with a direct impact on reducing medication errors; • Implementation of pharmaceutical interventions with a high acceptance rate, reducing drug-related problems and care-related risks; • Antimicrobial Stewardship management, promoting optimization of antimicrobial therapy and improvement of clinical outcomes; • Management of non-formulary medications, promoting resource optimization and supporting clinical decision-making; • Planning and delivery of technical training sessions, promoting staff qualification and reduction of non-compliance; • Coordination of the pharmacy team, with process standardization and improvement of operational efficiency.

• Technical review of documents related to the Specialized Component of Pharmaceutical Care (CEAF), ensuring technical quality; • Preparation of technical reports, promoting data systematization and supporting decision-making; • Integrated involvement in scientific communication, supporting review, production, and dissemination processes of technical content, with a focus on quality and public health impact; • Scientific coverage of events, including content production, fostering knowledge dissemination and institutional records; • Support for the editorial activities of the Journal of Pharmaceutical Care and Pharmacoeconomics, contributing to editorial quality and continuous process improvement; • Support in the journal indexing process in databases, contributing to increased visibility and scientific dissemination.

• Participation in the hospital implementation process, supporting the structuring of pharmacy workflows, stock organization, and alignment with good sanitary practices; • Participation in the Joint Commission International (JCI) accreditation process, collaborating on actions focused on patient safety and regulatory compliance; • Involvement in the implementation of the pharmacovigilance service, expanding monitoring, active surveillance, and adverse event reporting, with a positive impact on quality indicators; • Medication reconciliation, reducing discrepancies between prescriptions, preventing medication errors, and ensuring continuity of prior treatment; • Conducting audits of the medication-use process, contributing to continuous process improvement and medication safety across all stages of the medication workflow; • Control of medication and hospital supplies inventory, with a focus on expiration date management, promoting a 20% cost reduction and optimization of supplies; • Support in the analysis of quality indicators, contributing to performance monitoring and identification of opportunities for continuous improvement; • Training of the multidisciplinary team on the stages of the medication-use process in the hospital setting; • Assistance in prescription validation and in the compounding process of oncology medications, in accordance with good compounding practices.

• Participation pharmacogenetics research projects, with direct contribution to scientific data generation and analysis, resulting in publications in scientific journals; • Structuring and organization of pharmacogenetic databases, ensuring data integrity and standardization for scientific analyses; • Application of quality control measures to laboratory data, ensuring reliability, consistency, and analytical robustness of results; • Human DNA extraction, genotyping, and ELISA, following standardized protocols and good laboratory practices; • Analysis and interpretation of associations between genetic variants and clinical outcomes; • Preparation of technical and scientific reports, contributing to results documentation, project organization, and communication of findings; • Recruitment and follow-up of patients participating in scientific projects, in accordance with ethical standards.

• Participation in a research project at a biological medicines infusion center, from protocol development and submission to the Research Ethics Committee (CEP); • Recruitment and follow-up of patients with autoimmune diseases; • Monitoring adherence to pharmacological treatment with immunobiologics, contributing to the assessment of therapeutic effectiveness; • Application and analysis of quality-of-life assessment instruments, supporting the measurement of clinical outcomes and evaluation of treatment impact; • Medical record review, ensuring completeness and consistency of clinical information; • Data collection and structuring of the database; • Support in pharmaceutical assessment and dispensing of biological medicines; • Preparation of technical reports, contributing to results documentation and continuous improvement of research processes.

• Dispensing of medications listed in the Municipal Essential Medicines List (SUS) at a multi-center public health facility, in compliance with sanitary regulations, ensuring access to essential medicines; • Prescription review, ensuring legal and technical compliance; • Pharmaceutical counseling for patients, promoting treatment adherence and understanding of pharmacotherapy; • Medication inventory management, ensuring stock accuracy and resource optimization.

• Contract control; • Training control; • Descriptive standardization of materials; • Materials requisition; • Training organization.