Clinical Research Associate

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

📋 Description

• Conduct site qualifications, initiation, monitoring, and close-out visits for clinical trials.

• Ensure compliance with protocols, maintain data integrity, and prioritize patient safety throughout the trial process.

• Collaborate with investigators and site personnel to ensure the smooth execution of studies.

• Perform data reviews and resolve queries to uphold high-quality clinical data.

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

• Take charge of clinical trial monitoring deliverables and work in a cooperative manner.

⛳️ Requirements

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

• A minimum of 1 year of experience as a Clinical Research Associate.

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

• Excellent organizational and communication skills, with a keen eye for detail.

• Capability to work both independently and as part of a team in a fast-paced setting.

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

• Legal authorization to work in Australia.

🏝️ Benefits

• Competitive base salary along with performance-related incentives.

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

• Retirement and pension plans.

• Life assurance and disability coverage.

• Employee assistance programs and wellness resources.

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