This is a fully remote position, open to applicants in Australia.

📋 Description

• Perform site qualification, initiation, monitoring, and close-out visits for clinical trials.

• Ensure adherence to protocols, data integrity, and patient safety throughout the trial lifecycle.

• Work in partnership with investigators and site personnel to ensure efficient study execution.

• Conduct data reviews and address queries to uphold high standards of clinical data quality.

• Assist in the preparation and evaluation of study documentation, including protocols and clinical study reports.

⛳️ Requirements

• A Bachelor's degree in a scientific or healthcare-related discipline.

• At least 2 years of experience as a Clinical Research Associate.

• Comprehensive understanding of clinical trial processes, regulations, and ICH-GCP guidelines.

• Excellent organizational and communication abilities, with a keen attention to detail.

• Capability to work both independently and collaboratively in a dynamic environment.

• Willingness to travel a minimum of 60% of the time (both international and domestic - by air and road).

• A valid driver's license.

• Legal authorization to work in Australia.

🏝️ Benefits

• Competitive base salary along with performance-based incentives.

• Health and wellness programs, including medical, dental, and vision coverage where applicable.

• Retirement and pension schemes.

• Life insurance and disability coverage.

• Employee assistance programs and wellness resources.

• Opportunities for learning and development through structured training and career advancement pathways.