Jundiaí, São Paulo, Brazil
🌿 I worked as a specialist nurse in Oncology, Onco‑Hematology and Cell Therapy, with over 25 years of experience in high‑complexity care settings. I have been driven by a strong passion for oncology, scientific rigor and evidence‑based decision‑making. I exercised team leadership, guiding and developing multidisciplinary teams in challenging environments. I built strong skills in self‑management, organization, prioritization and adaptability in dynamic settings, working independently and in collaborative cross‑functional teams. 🌿 Clinical Research – Phase I–IV: I led Phase I–IV clinical studies at the UNICAMP Hemocenter, where I structured and consolidated a research center. I conducted feasibility assessments, analyzing protocols, eligible populations, operational capacity and risks. I developed effective patient recruitment and retention strategies, integrating clinical teams, optimizing workflows and strengthening communication with participants. I ensured adherence to SOPs, GCP‑ICH and international standards, guaranteeing high‑quality data. I managed budgets, governance, audits and relationships with ethics committees and regulatory authorities, acting proactively in risk mitigation, problem‑solving and barrier removal to ensure strong site performance. 🌿 Leadership and Stakeholder Engagement: I trained multidisciplinary teams, promoting clear communication, critical thinking and a collaborative culture. I built strong relationships with internal and external stakeholders, influencing without formal authority and conducting high‑impact interactions with KOLs. I maintained consistent performance in regulated environments, with a strong sense of responsibility and compliance. 🌿 Medical Science and Medical Affairs: I worked as an MSL and scientific advisor, leading scientific initiatives, strategic projects and technical training, including cell therapy programs. My work was strongly cross‑functional, collaborating with Clinical Research, Market Access, Marketing, Regulatory Affairs, Compliance and Commercial teams to ensure scientific alignment and strategic impact. I contributed to oncology therapeutic launches and globally recognized projects. I used advanced communication skills in English and proficiency in Spanish for scientific and regional interactions, with availability for travel across Brazil and Latin America. 🌿 I am seeking opportunities in Clinical Research, Medical Affairs and scientific leadership in environments that value operational excellence, critical thinking and a genuine commitment to patient care.
🌿Expertise in Onco‑Hematology🌿 Stakeholder Engagement and Relationship Building: I actively participated in scientific discussions with healthcare professionals, fostering high‑level exchanges and deepening the technical quality of interactions. I worked cross‑functionally with internal teams, providing strategic scientific support to strengthen the portfolio and guide decision‑making. Scientific Management and Portfolio Oversight: I contributed to the active management of an onco‑hematology portfolio, ensuring scientific and technical alignment with national and international guidelines. I handled scientific and regulatory demands for products, ensuring compliance, accuracy, and consistency with quality and safety standards. Scientific Activities and Patient Safety: I conducted evidence‑based scientific activities with a strong focus on patient safety and the practical application of best clinical practices. I continuously assessed scientific needs, contributing to greater adherence to therapeutic guidelines and supporting more informed clinical decision‑making. Medical Materials and Compliance: I adapted, reviewed, and validated medical and scientific materials, ensuring accuracy, consistency, and regulatory compliance. I elevated the quality of content used by internal teams and healthcare professionals, reinforcing credibility and trust. Key Achievements: - Strengthened scientific and technical alignment in onco‑hematology. - Enhanced protocols and practices focused on patient safety. - Improved regulatory adherence and the quality of scientific materials. - Increased the precision and reliability of information used in patient care. - Encouraged the practical application of therapeutic guidelines in clinical settings. - Elevated the effectiveness of scientific discussions with healthcare professionals. - Contributed strategically to portfolio development and sustainability through robust scientific insights.
🌿 Strategic Engagement in Hematology – Scientific Management, Clinical Studies, and Medical Engagement 🌿 Scientific Management and Portfolio Oversight: I managed a complex hematology portfolio, ensuring consistency, scientific rigor, and strategic alignment with clinical and regulatory guidelines. I evaluated clinical data and regulatory requirements to guide decision‑making and strengthen product strategy. Medical Engagement and Therapeutic Discussions: I built and strengthened relationships with key physicians, leading high‑quality therapeutic discussions and deepening the technical level of scientific interactions. I promoted impactful scientific exchanges that supported clearer and more informed clinical decision‑making. Integration with Clinical Research and Leadership in Studies: I acted as a bridge between Clinical Research and Medical Affairs, ensuring scientific alignment across studies and leading technical aspects of relevant research initiatives. I contributed to study efficiency through scientific engagement, recruitment support, and close follow‑up of site needs. Training, Compliance, and Best Practices: I delivered scientific training on clinical data, safety, and best practices, elevating team knowledge and performance. I ensured compliance with regulatory and scientific standards, strengthening process integrity and the quality of deliverables. Key Achievements: - Optimized portfolio management protocols in hematology. - Ensured regulatory and scientific compliance across the portfolio. - Elevated the quality of interactions with key physicians. - Secured technical and regulatory alignment in clinical studies. - Expanded recruitment and technical engagement in research. - Improved training outcomes with a focus on safety. - Strengthened scientific events focused on hematology updates.
🌿 Strategic Role as an MSL in Onco‑Hematology 🌿 I conducted scientific activities in oncology and hematology with a strong evidence‑based approach, working across melanoma, renal carcinoma, lymphoma, multiple myeloma, and myelodysplastic syndromes. I ensured technical depth and consistency in scientific discussions with healthcare professionals. I structured scientific and operational processes for a newly implemented medical area, creating workflows that supported efficiency, governance, and quality. I provided scientific support for therapeutic safety during new product launches, ensuring precise communication aligned with best practices. I acted as a bridge between Clinical Research and Medical Affairs, ensuring scientific alignment across studies and leading integrated initiatives with other MSLs. I contributed to operational efficiency through scientific engagement, recruitment support, and close follow‑up with study sites. I engaged healthcare professionals to improve study execution, identify risks, and enhance data quality. I supported the Expanded Access Program, helping deliver innovative therapies to patients without alternatives. I collaborated closely with internal teams, maintaining focus on shared strategic objectives. Key Achievements: - Strengthened scientific rigor in onco‑hematology discussions. - Structured processes that ensured efficiency and consistency. - Reinforced therapeutic safety in new product launches. - Enhanced the quality of evidence‑based scientific discussions. - Increased scientific consistency in clinical research communication. - Reduced response times in collaborative projects. - Improved clinical study efficiency through qualified engagement. - Enabled access to innovative therapies. - Led educational programs for the safe use of new therapies. - Contributed strategically to pre‑launch and launch activities.
🌿 Strategic Role as a Clinical Research Leader 🌿 Structure and Governance: I led the development of a Clinical Research Center, defining strategy, governance, processes, operational workflows, and SOPs. I implemented practices aligned with global standards, ensuring efficiency, sustainability, and institutional maturity. Excellence in ICH‑GCP and Compliance: I operated in full compliance with ICH‑GCP, ensuring quality, patient safety, and data integrity. I maintained alignment with IRB/EC and ANVISA requirements, strengthening national and international regulatory adherence. Management of High‑Complexity Studies: I coordinated more than 30 clinical studies, overseeing execution, timelines, audits, and regulatory compliance. I managed data collection, analysis, and consolidation, ensuring traceability, consistency, and scientific excellence. Feasibility, Ethics, and Critical Analysis: I assessed technical, scientific, operational, and financial feasibility, conducting critical analyses from ethical and regulatory perspectives. I made strategic decisions that preserved institutional integrity and optimized resources. Multidisciplinary Leadership and Recruitment: I led clinical, scientific, and administrative teams, promoting performance, compliance, and high‑quality delivery. I implemented strategies that increased patient recruitment and retention, strengthening operational efficiency. Key Achievements: - Implemented a high‑complexity clinical research center aligned with global standards. - Ensured consistent compliance with ICH‑GCP and regulatory requirements. - Secured ethical, scientific, and regulatory cohesion across a diverse portfolio. - Maintained high standards of data quality and reliability. - Structured robust governance and efficient budget and resource management. - Strengthened relationships with regulatory authorities and compliance bodies. - Received international recognition for clinical research credibility.
🌿 Advanced Clinical Practice, Applied Research, Evidence‑Based Medicine, Real‑World Analysis 🌿 Specialized Care in High‑Complexity Settings: I worked in a high‑complexity onco‑hematology care environment, providing direct care to patients with critical clinical needs. I maintained a strong focus on patient safety, therapeutic management, treatment adherence, clinical effectiveness, and evidence‑based decision‑making, ensuring clinical stability and high‑quality care. Transforming Clinical Practice into Applied Research: I translated real‑world clinical demands into structured clinical studies, developing protocols that reduced infectious risks and elevated standards of care. I led initiatives integrating clinical practice, research, and innovation, strengthening therapeutic safety and effectiveness. Clinical Research with Innovative Therapies: I conducted clinical research involving oral tyrosine‑kinase inhibitors, analyzing treatment adherence, therapeutic response, and clinical impact on patient outcomes. My work contributed to understanding adherence patterns and optimizing therapeutic strategies. Protocol Development and Therapeutic Optimization: I developed personalized care protocols based on in‑depth analysis of clinical data, promoting greater treatment effectiveness and standardized clinical practices. I strategically designed workflows that enhanced safety and efficiency in patient care. Data Management, Ethics, and Research Governance: I coordinated clinical data collection, monitoring, and analysis, ensuring traceability, quality, and methodological consistency. I maintained direct patient interaction and managed all regulatory processes with the ethics committee, ensuring compliance and scientific rigor.
🌿 Specialized Clinical Care and Operational Leadership in Hematology, Oncology, and Cellular Therapy 🌿 I provided direct care to patients in oncology, hematology, and bone marrow transplantation, with deep practical knowledge of patient clinical status, therapeutic journey, access barriers, toxicity management, and real needs throughout treatment. I ensured continuous, safe, high‑complexity care focused on risk prevention, complication management, and humanized support. I led and coordinated nursing teams, structuring routines, assigning responsibilities, and ensuring consistent execution of institutional protocols. I strengthened team integration, improved internal communication, and aligned care practices with quality goals and safety guidelines — always considering the impact of therapies and access on clinical outcomes. I contributed to clinical excellence through close patient follow‑up and continuous technical support to the team. I served as a reference for decision‑making, best‑practice guidance, training in complex procedures, and development of essential competencies for specialized care, integrating practical knowledge of therapies, adherence, and clinical response. I identified opportunities to improve care workflows and supported the implementation of processes that enhanced safety, standardization, and efficiency. My work strengthened care quality, optimized resources, and contributed to a more organized, effective, and results‑oriented clinical environment — always centered on the real patient journey and therapeutic effectiveness.