CRA II: Remote Clinical Trial Monitoring & Data Integrity
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Benefits offered by this job
Job summary
ICON Strategic Solutions in Melbourne, Australia is seeking a CRA II for a remote role. You will design and analyse clinical trials, interpreting complex data and contributing to the development of innovative treatments that benefit patients worldwide.
This sponsor-dedicated position requires 2+ years of CRA experience, ICH-GCP knowledge, and strong organizational skills. You will travel approximately 60% and collaborate with investigators and site staff to ensure study success.
Qualifications
- Bachelor's degree in a scientific or healthcare-related field.
- Minimum 2 years of experience as a Clinical Research Associate.
- In-depth knowledge of clinical trial processes, regulations, and ICH-GCP.
- Willingness to travel ~60% and strong organizational skills.
Responsibilities
- Conduct site qualification, initiation, monitoring, and close-out visits.
- Ensure protocol compliance, data integrity, and patient safety.
- Collaborate with investigators and site staff to facilitate study conduct.
- Perform data review and resolve queries to maintain data quality.
- Contribute to preparation and review of study documents (protocols, reports).
Skills
Education
Job description
ICON Strategic Solutions in Melbourne, Australia is seeking a CRA II for a remote role. You will design and analyse clinical trials, interpreting complex data and contributing to the development of innovative treatments that benefit patients worldwide.
This sponsor-dedicated position requires 2+ years of CRA experience, ICH-GCP knowledge, and strong organizational skills. You will travel approximately 60% and collaborate with investigators and site staff to ensure study success.
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