Senior CRA

TFS HealthScience is seeking a Freelance Senior Clinical Research Associate (0.4 FTE) to support ophthalmology studies from home in Italy.L'esperienza richiesta ai candidati, così come le competenze e le qualifiche aggiuntive necessarie per questo lavoro, sono elencate di seguito.The role involves on-site or remote monitoring, protocol compliance, and...

Syneos Health, Inc.Possiede le competenze per ricoprire questo ruolo? Legga i dettagli completi qui sotto e invii la sua candidatura oggi stesso.is seeking a Sponsor Dedicated CRA II/Sr CRA I/II for a home-based role in Italy.The candidate will perform site qualification, initiation, monitoring and close-out visits (on-site or remotely) while ensuring...

Trial Form Support is seeking a remote Clinical Trial Monitor specializing in oncology to oversee site monitoring, data integrity, and regulatory compliance across global sites.Prima di candidarsi per questo ruolo, la preghiamo di leggere le seguenti informazioni su questa opportunità, riportate di seguito.You will ensure patient safety, validate informed...

TFS HealthScience seeks a Clinical Research Associate (CRA) to join our team as a home-based professional in Italy.Qualifiche, competenze e l'esperienza necessaria per questo ruolo sono disponibili nella descrizione completa riportata di seguito.You will monitor sites, ensure subject safety and data integrity, and ensure compliance with GCP/ICH guidelines....

TFS HealthScience is seeking a Freelance Senior Clinical Research Associate (0.4 FTE) home based in Italy to support ophthalmology studies. You will monitor sites on-site and remotely, ensure GCP/ICH compliance, and maintain data integrity.The role requires a Bachelor’s degree, >5 years on-site monitoring, and ophthalmology experience; fluency in English...

Syneos Health, Inc. is seeking a Sponsor Dedicated CRA II/Sr CRA I/II for a home-based role in Italy. The candidate will perform site qualification, initiation, monitoring and close-out visits (on-site or remotely) while ensuring regulatory and GCP compliance and robust data integrity. Applicants should have at least 2.5 years as a certified CRA, oncology...

Trial Form Support seeks a capable Clinical Trial Monitor to oversee oncology trials across sites, ensuring patient safety, data integrity, and regulatory compliance from a home-based setting.Verifichi che le sue competenze e la sua esperienza corrispondano ai requisiti di questo ruolo, quindi si candidi con il suo CV qui sotto.You will coordinate monitoring...

Translational Research in Oncology (TRIO) in Italy is seeking a Senior Clinical Research Associate to join our Monitoring Resources team. The role is home-based in Italy and reports to a CRA Line Manager. You will conduct site visits, ensure regulatory compliance, and mentor junior CRAs. Fluency in English and a science-related Bachelor's degree are...

WhatYou'llDo: Serve as main CTI contact for assigned study sites Conduct site visits (pre-study [PSV], site initiation [SIV], interim monitoring [IMV], and close-out [COV]) and complete site visit deliverables with quality and within given timelines in Monitoring Plan while adhering to all applicable regulatory requirements, SOPs and ICH GCP Assist with or...