Clinical Research Associate II/Senior CRA

Clinical Research Associate II/Senior CRA

ICON

Prague, Czech Republic

We are currently seeking a Clinical Research Associate II to join our diverse and dynamic team. As a Clinical Research Associate II at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies.

What you will be doing

• Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials;
• Ensuring protocol compliance, data integrity, and patient safety throughout the trial process;
• Collaborating with investigators and site staff to facilitate smooth study conduct;
• Performing data review and resolution of queries to maintain high-quality clinical data;
• Contributing to the preparation and review of study documentation, including protocols and clinical study reports.

Your profile

• Bachelor's degree in a scientific or healthcare-related field;
• Minimum of 2 years of experience as a Clinical Research Associate;
• 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;
• Ability to travel at least 60% of the time (international and domestic - fly and drive) and should possess a valid driver’s license.