Clinical Research Associate

Overview

In this role, you contribute to the design and analysis of clinical trials within ICON’s sponsor-dedicated model. You will monitor sites, ensure protocol adherence, data integrity, and patient safety, and collaborate with investigators to ensure smooth study conduct. You’ll review data, resolve queries, and help prepare study documents to support trial quality. This is a role that combines hands-on monitoring with cross-functional teamwork to advance treatments for patients globally.

Retribuzione / Benefits

Competitive base salary

Health and wellbeing programmes including medical, dental, and vision coverage where applicable

Retirement and pension plans

Life assurance and disability coverage

Employee assistance programmes and wellbeing resources

Learning and development opportunities through structured training and career pathways

Responsabilità

Conduct site qualification, initiation, monitoring, and close-out visits for clinical trials

Ensure protocol compliance, data integrity, and patient safety throughout the trial process

Collaborate with investigators and site staff to facilitate smooth study conduct

Perform data review and resolution of queries to maintain high-quality clinical data

Contribute to the preparation and review of study documentation, including protocols and clinical study reports

Requisiti fondamentali

Bachelor's degree in a scientific or healthcare-related field

Minimum of 2 years of experience as a Clinical Research Associate after being certified as per Italian Decree

In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines

Strong organizational and communication skills, with attention to detail

Ability to work independently and collaboratively in a fast-paced environment

Employment eligibility to work in the role's country

strong communication

attention to detail

team collaboration

clinical trial monitoring

data review and query resolution

ICH-GCP knowledge