Beatriz Curiel Rollón Email & Phone Number

Therapeutic Area: Oncology, particularly dedicated in clinical trials related to breast cancer (Metastatic, Neoadjuvant, and Adjuvant Breast Cancer).• Perform visits to support CRAs in clinical trials for Phase II, Phase III trials, and observational studies during start-up, monitoring, and study close-out visits.• Ensuring assigned studies comply with regulatory requirements, protocol, company SOPs, and ICH-GCP guidelines.• Maintaining drug accountability throughout the research process.• Verification and review of Adverse Events (AES), Serious Adverse Events (SAEs), and concomitant medication according to the protocol.• Reviewing the archive of sites following Good Clinical Practices (GCPs) for compliance.• Offering guidance to site staff for timely query resolution.• Completing monitoring reports according to SOPs and Sponsor requirements.

Madrid, Comunidad De Madrid, España

Máster, Monitorización De Ensayos Clínicos

Máster, Forensic Psychology

Grado, Psychology