Senior CRA

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...

Worldwide Clinical Trials is seeking a Clinical Research Associate for a home‐based role supporting sites across Italy.Massimizzi le sue possibilità di successo assicurandosi che il suo CV e le sue competenze corrispondano ai requisiti di questa posizione.You will monitor trials, ensure quality and regulatory compliance, and partner with investigative...

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...

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...

Worldwide Clinical Trials is seeking a Clinical Research Associate for a home‑based role supporting sites across Italy. You will monitor trials, ensure quality and regulatory compliance, and partner with investigative sites and sponsors to drive data integrity.Ideal candidates have 3+ years of CRA experience, strong knowledge of GCP/ICH, and fluency in...

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. You will ensure patient safety, validate informed consent, and manage trial documentation in line with GCP/ICH standards.In this home-based role, you will coordinate monitoring...

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. You will ensure patient safety, validate informed consent, and manage trial documentation in line with GCP/ICH standards.In this home-based role, you will coordinate monitoring...

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. You will coordinate monitoring activities, manage documentation, and support audits to enable successful study execution.The role requires at least 3 years in...