Aurora DeOliveira

• Managed clinical trial protocols and ensured compliance with regulatory standards.
• Collaborated with cross-functional teams to facilitate study initiation and execution.
• Supervised data collection processes and maintained quality control measures.
• Developed training materials for research staff and conducted educational sessions.
• Strategic budget allocation management for clinical research programs.
• Worked closely with sponsors to facilitate initiation visits and ensure successful ongoing monitoring.
• Analyzed trial data and prepared reports for stakeholders.
• Ensured adherence to ethical guidelines throughout the research process.
• Coordinated with external vendors to ensure timely and accurate collection and delivery of data results.
• Organized and conducted study site meetings to ensure compliance with protocol requirements.
• Reviewed data from clinical trials for accuracy and completeness.
• Liaised with pharmaceutical companies regarding drug supply arrangements for studies.
• Conducted quality assurance reviews of the study site to ensure adherence to Good Clinical Practices.
• Analyzed study results to identify trends or areas needing further investigation.
• Developed training materials for clinical research staff on GCPs, ICH guidelines, and other relevant topics.
• Collaborated with medical writers to prepare documents required by regulatory agencies including informed consent forms, annual reports, and investigator brochures.
• Facilitated resolution of discrepancies between source documentation and CRFs.
• Developed and managed clinical research protocols, budgets, and project timelines.
• Provided guidance on regulatory issues related to clinical research projects.
• Generated monthly progress reports detailing enrollment numbers, site performance metrics.
• Maintained communication between sponsors, investigators, IRBs and ethics committees, contract research organizations, and other stakeholders involved in a study.
• Ensured that all adverse events were reported promptly according to FDA regulations.
• Coordinated the collection and analysis of safety data in accordance with FDA regulations.
• Monitored patient recruitment progress, identified and applied strategies for improvement, with a patient retention of 99% after sutdy enrollment.
• Prepared detailed case report forms outlining data collection requirements for each trial participant.
• Monitored patient reactions to drugs and carefully documented progress of individuals participating in clinical trials.
• Educated participants on studies and anticipated outcomes.
• Conducted screening interviews to determine eligibility of possible subjects.
• Collaborated with sponsors and investigators to carry out efficient and fully compliant research trials.
• Assessed records of each patient, reviewed databases and checked referrals to locate potential research study participants.
• Kept patient care protocols and clinical trial operations in compliance.
• Took vital signs and collected medical histories as part of study protocols.

• Oversee curriculum development, implementation, and continuous improvement of the Ophthalmology Program
• Ensure compliance institutional policies and accreditation standards.
• Recruit, interview, and select residents.
• Supervise, mentor, and evaluate residents across all levels of training.
• Conduct regular evaluations of faculty teaching performance and provide feedback..
• Facilitate scholarly activity among residents and ensure compliance with scholarly requirements.
• Coordinate with other departments for multidisciplinary training experiences.
• Serve as a liaison with hospital administration and affiliated training sites.

• Diagnosed and treated various ocular diseases and conditions effectively.
• Performed surgical procedures.
• Collaborated with healthcare staff to develop patient care plans.
• Educated patients on eye health, treatment options, and preventive measures.
• Utilized advanced diagnostic equipment for precise vision assessments.
• Developed patient management plans based on diagnosis and prognosis.
• Maintained accurate patient records and documentation in electronic systems.
• Provided emergency eye care services for urgent cases requiring immediate attention.
• Documented all clinical findings in electronic medical records system.
• Analyzed test results to determine appropriate course of action for each patient's condition.
• Performed comprehensive ophthalmologic examinations, including slit-lamp biomicroscopy, fundus photography, visual field testing and tonometry.
• Interpreted imaging studies such as CT scans or MRIs to diagnose conditions affecting the eyes.
• Provided preoperative and postoperative care for patients undergoing cataract surgery or other procedures.
• Maintained current knowledge of advances in ophthalmology through continuing education courses.

• Provide comprehensive internal medicine care for hospitalized COVID-19 patients.
• Monitor disease progression and manage complications such as ARDS, sepsis, and thromboembolic events.
• Collaborate with infectious disease specialists, intensivists, respiratory therapists, and nursing staff.
• Initiate and manage COVID-specific therapies in accordance with institutional protocols (e.g., antivirals, corticosteroids, monoclonal antibodies).
• Participate in rounds, family communications, and care planning discussions.
• Ensure strict adherence to PPE usage and infection control protocols.
• Support and educate junior medical staff and residents.
• Participate in clinical documentation and quality assurance efforts.

Developed and authored 10 studies and technical reports analyzing services provided by the Brazilian Public Health System, with a focus on current public policies, federal budgeting, and projections for materials and resource allocation.

• Collected, analyzed, and interpreted data from diverse sources—including medical histories, electronic health records, billing claims, and cost reports—to support evidence-based decision-making.
• Pioneered, the first approved off-label use of Bevacizumab for retinal disease treatment in Brazil.

• Analyzed study data to support national health policies and initiatives.
• Managed regulatory affairs and clinical trial analysis across Phases I–IV to ensure protocols, case report forms (CRFs), and data collection tools complied with applicable regulatory requirements.
• Developed training materials and conducted workshops and meetings with pharmaceutical sponsors, study sites, investigators, and internal teams.
• Conducted site monitoring activities, supervised assigned CRAs, and conducted site and study audits.