Clinical Research Associate

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

📋 Description

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

• Ensure adherence to protocols, maintain data integrity, and prioritize patient safety throughout the study lifecycle.

• Collaborate with investigators and site personnel to ensure effective study execution.

• Conduct data reviews and resolve queries to uphold the quality of clinical data.

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

• Operate within a sponsor-dedicated framework supported by ICON’s global expertise.

⛳️ 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 eye for detail.

• Capability to work both independently and as part of a team in a dynamic environment.

• Willingness to travel a minimum of 60% of the time (both internationally and domestically - via flight and driving).

• Valid driver's license.

• 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 insurance and disability coverage.

• Employee assistance programs and wellness resources.

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