Alex Boluda

Managed home-based clinical trial visits, including medication administration, vital signs monitoring, and adverse event (AE/SAE) reporting. Collaborated with multidisciplinary healthcare teams and provided patient education, emotional support, and protocol compliance. Supported data collection and entry in eCRF/EDC, contributing to accurate trial documentation.

Managed medication administration, vital signs monitoring, and AE/SAE reporting for pediatric clinical trial participants in home-based settings." Performed specialized pediatric laboratory procedures, including phlebotomy, centrifugation, and pipetting, ensuring high-quality sample processing and protocol compliance." Provided emotional support and therapeutic education to pediatric patients and their families, facilitating treatment adherence and safety.

Sponsor-Site Liaison: Acting as a direct link between the Sponsor and the clinical site to streamline trial execution and reduce administrative burden. Data Integrity: Managing eCRF/EDC data entry and weekly source document reviews to ensure "monitor-ready" (Pre-SDV) clinical data. Query & AE Management: Proactively resolving data discrepancies and Queries; supporting AE/SAE reporting prior to monitoring visits. Monitoring Support: Providing on-site assistance during monitoring visits to ensure ICH-GCP compliance and data veracity.

Technichal Support for a new digestive treatment. The treatment is administered in the operating theatre.

Conducted sample collection and processing for an immunology clinical trial. Coordinated with the research team and provided operational support to ensure smooth trial execution and protocol compliance.

Led patient recruitment, screening, and informed consent for internal medicine, endocrinology, and medical device trials. Managed eCRF data entry, resolved queries, and maintained Investigator Site File (ISF) for GCP compliance. Coordinated site operations, patient visits, and multidisciplinary team communication. Performed advanced phlebotomy, sample processing, and shipment for clinical trials. Supported multicenter trial oversight, site start-up, and feasibility assessments. Monitored and reported Adverse Events (AE/SAE) per protocol and regulatory requirements.

Conducted telephone-based patient screening and recruitment for clinical trials. Performed in-depth medical interviews, assessed patient eligibility based on medical history, and guided potential participants on trial enrollment. Provided patient counseling and support throughout the selection process.

Conducted comprehensive patient searches using hospital databases and emergency department screening to identify candidates meeting inclusion criteria for COVID clinical trial. Led patient recruitment and enrollment via telephone and in-person visits, scheduling appointments and ensuring protocol adherence. Performed blood draws, sample processing, and treatment administration, followed by ongoing patient follow-up through home and telephone visits. Entered and maintained accurate clinical trial data in REDCap/CRD, including AE/SAE reporting, ensuring compliance with GCP and protocol requirements. Demonstrated full autonomy in managing trial activities, combining clinical skills, patient interaction, and data management to support smooth study execution.

Guardias esporádicProvided emergency and clinical care in a mobile medicalized ambulance setting, attending patients outside the hospital environment. Gained experience in rapid clinical assessment, patient monitoring, and critical interventions, demonstrating autonomy and adaptability in extrahospitalary care.as.

Participated in a COVID-19 immunoglobulin clinical trial as a Blinded Home Visit Nurse, supporting multiple study sites. Conducted home visits, performing venipuncture, vital signs monitoring, and basic life support. Managed visit documentation and worksheets, ensuring accurate and timely data capture. Progressed to patient recruitment, screening candidates for eligibility and coordinating enrollment. Collaborated with multiple sites, contributing to smooth trial operations and compliance with protocol and GCP standards.

Advanced training in clinical trial coordination, site management, and regulatory compliance, preparing for CRA and CRC roles. Focused on monitoring patient recruitment, data quality, and trial documentation, with emphasis on decentralized/home-based studies. Builds competencies to support multi-site trials, manage study operations, and enhance protocol adherence.

EU Gimbernat Mención en innovación y gestión de la diversidad en la enfermería.

Incluye SVA SVAT y prácticas en SEM

Trained in medical imaging techniques, including X-ray, MRI, and CT scans (RMN/TAC). Developed patient positioning, safety protocols, and imaging workflow skills. Applied technical expertise to support clinical procedures and diagnostics.