Sandra Yebes del Pino
Resumen profesional
During the last 4 years, I have been focusing on my career in the field of ONCOLOGY CLINICAL TRIALS in PHASE I as a study coordinator at START CIOCC MADRID and PHASE II and III as a CLINICAL RESEARCH ASSOCIATE at AbbVie. After more than a decade working as an operating room nurse, being part of different surgical teams, and serving as a supervisor for the operating room and surgical sub-areas, leading teams of 40-50 people, I decided to further my education and immerse myself in the fascinating world of clinical trials . I am searching new opportunities of work in the industry to continue developing my knowledge and in addition of that continue helping people.
Datos destacados
3
3
years of professional experience
Experiencia
Clinical Research Associate
AbbVie
Madrid, Madrid
01.2024 - Actual
- Monitoring Clinical Trials: Ensure that clinical trials in oncohematology are conducted in compliance with regulatory requirements and protocols.
- Site Visits: Conduct regular site visits to oversee the progress of studies, addressing any issues that arise.
- Data Integrity: Verify the accuracy and completeness of clinical data and ensure its secure documentation.
- Collaboration: Work closely with site staff, including investigators and clinical teams, to support study conduct and address any challenges.
- Participant Management: Assist with the recruitment, enrollment, and follow-up of study participants, ensuring their safety and well-being.
- Regulatory Compliance: Ensure that all aspects of the clinical trial adhere to ethical standards and regulatory guidelines.
- Training and Support: Provide training and ongoing support to site personnel to ensure effective study execution.
- Communication: Facilitate clear and ongoing communication between study sites and the sponsor or clinical trial management team.
Study Coordinator, Research Nurse
START CIOCC MADRID
05.2021 - 01.2024
- Coordination and Supervision: Coordinate and supervise clinical or research studies, specifically Clinical Oncology Trials Phase I at CIOCC Madrid.
- Documentation Management: Organize and maintain study-related documentation and records.
- Collaboration: Collaborate with the research team for planning and executing study protocols.
- Protocol Compliance: Ensure adherence to applicable protocols and regulations.
- Participant Screening: Coordinate screening and eligibility activities of study participants.
- Data Management: Conduct real-time data tracking, collection, and sample management, including collection and shipment.
- Communication: Manage communication and follow-up with study participants, and coordinate visits and schedules.
- Reporting: Prepare reports and present results clearly and accurately.
- Confidentiality: Maintain confidentiality and safeguard the privacy of participants.
- Query Resolution: Address and resolve queries from monitors and other stakeholders.
- Stakeholder Communication: Communicate with monitors from various CROs and sponsors, providing patient updates and participating in teleconferences.
Formación
DEGREE ONCOLOGIST NURSE - ONCOLOGIST NURSE
EUROPEAN SCHOOL OF HEALTH
MONITORING CLINICAL TRIAL MASTER - CLINICAL TRIALS
UNIR
DEGREE - NURSING
Universidad San Pablo CEU
Enfatiza tus habilidades clave
- Ability to communicate and organaize
- Write reports
- Knowledge of medical records and medical terminology
- Teamwork and training
- Administrative management
- Skills for building and managing teams
- High ability to make decisions in difficult situations to manage
- MICROSOFT OFFICE
Idiomas
Español
Idioma nativo
Inglés
Avanzado
C1
Francés
Básico
A2
Personalizado
2,A2,4,B2
Cronología
Clinical Research Associate
AbbVie
01.2024 - Actual
Study Coordinator, Research Nurse
START CIOCC MADRID
05.2021 - 01.2024
DEGREE ONCOLOGIST NURSE - ONCOLOGIST NURSE
EUROPEAN SCHOOL OF HEALTH
MONITORING CLINICAL TRIAL MASTER - CLINICAL TRIALS
UNIR
DEGREE - NURSING
Universidad San Pablo CEU
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