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Sabrina Monzon

Sabrina Monzon

Clinical Research | Clinical Operations | Site Coordination

Talento
Puerto MadrynMiembro desde 3 de septiembre de 2026
Clinical research & clinical trialsBiological sample management & traceabilityStudy and patient coordinationQuality procedures and regulated processesProtocol and visit follow-upOperational coordination & problem solvingClinical documentation & recordsSINTRA information system
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Clinical research & clinical trialsBiological sample management & traceabilityStudy and patient coordinationQuality procedures and regulated processesProtocol and visit follow-up

Sobre mí

Healthcare professional with experience in operational coordination within organ procurement and transplantation, combined with previous experience as a Clinical Research Coordinator in Phase III oncology clinical trials. Strong background in patient and team coordination, clinical documentation, information systems, biological sample management and traceability, and regulated processes. Seeking to return to clinical research while bringing extensive healthcare coordination experience and the ability to learn new systems.

Experiencia

Operational Coordination, Organ Procurement & Transplantation at CUCAIBA (2018-01 – Present)

  • Coordinate teams involved in organ procurement and transplantation operations across different hospitals.
  • Enter, update and manage critical information in SINTRA, the national transplant information system.
  • Participate in organ allocation and distribution according to established criteria.
  • Coordinate post-procurement follow-up and communication among the teams involved.
  • Work with accuracy, traceability, confidentiality and standardized procedures.

Provincial Transplant Sample Repository (Seroteca) at CUCAIBA (2019-01 – Present)

  • Process, store and preserve biological samples.
  • Maintain sample traceability, records and storage conditions.
  • Manage documentation and comply with quality and procedural requirements.

Clinical Research Coordinator | Phase III Oncology Clinical Trials

Experience initially gained through a university fellowship and subsequently continued at a private oncology clinic.

  • Coordinated patient visits and study-related activities.
  • Coordinated with investigators, sub-investigators and specialized healthcare professionals according to study requirements.
  • Followed up on sub-investigator tasks and documentation within patient medical records.
  • Managed clinical research documentation and followed study protocols and requirements.

Educación

Technical Degree in Hemotherapy and Immunohematology

Habilidades

Clinical ResearchClinical OperationsSite Coordination

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