Travel‑Ready CRA II — Clinical Trials & Data Monitor

ICON Clinical Research; Sydney; Sur place; AUD 90 000 - 120 000; Plein temps

Résumé du poste

ICON Strategic Solutions in Sydney is seeking a CRA II to design and analyse clinical trials, interpret complex medical data, and contribute to treatments that benefit patients worldwide.

You will conduct site qualification, initiation, monitoring, and close-out visits, ensuring protocol adherence and patient safety, while collaborating with investigators and site staff to ensure smooth study conduct. Travel (~60%) is required.

Qualifications

• 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.
• Willingness to travel as required (approximately 60%).

Responsabilités

• 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

Connaissances

Organizational skills

Communication skills

Attention to detail

Independence

Team collaboration

Willingness to travel

Formation

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

Description du poste

ICON Strategic Solutions in Sydney is seeking a CRA II to design and analyse clinical trials, interpret complex medical data, and contribute to treatments that benefit patients worldwide.

You will conduct site qualification, initiation, monitoring, and close-out visits, ensuring protocol adherence and patient safety, while collaborating with investigators and site staff to ensure smooth study conduct. Travel (~60%) is required.