Clinical Research Associate

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

📋 Description

• Conduct Site Selection Visits, Site Initiation Visits, Interim Monitoring Visits, and Close-Out Visits.

• Ensure that investigator sites adhere to study protocols, ICH-GCP standards, sponsor requirements, and local regulations.

• Oversee patient safety, data integrity, and study documentation throughout the clinical trial lifecycle.

• Build and maintain relationships with investigators, site personnel, and sponsor stakeholders.

• Assist in site preparedness, subject recruitment, and resolving issues to meet study timelines.

• Identify, document, and escalate potential risks while supporting risk-based monitoring strategies.

• Aid in audit and inspection preparedness activities.

⛳️ Requirements

• A Bachelor's degree in Life Sciences, Nursing, Pharmacy, or a related discipline.

• At least 3 years of independent clinical monitoring experience in the pharmaceutical, biotechnology, or CRO sectors.

• Comprehensive knowledge of ICH-GCP guidelines and relevant regulatory standards.

• Proven experience in managing sites from initiation to close-out.

• Outstanding communication and relationship-building abilities.

• Proficiency in English, both written and spoken.

• Willingness and ability to travel frequently within the assigned country.

• A valid driving license.

🏝️ Benefits

• Opportunities for both personal and professional development.

• A rewarding work environment.

• A collaborative team culture.

• Applicable benefits.

• Opportunity to work with a global pharmaceutical company sponsor.

• A flexible clinical development and strategic resourcing environment.