Join as a Clinical Research Associate for Advanced Studies

Join a leading role in advancing clinical research as a Clinical Research Associate! Conduct critical monitoring of studies in phases II and III while ensuring compliance with industry standards.

This position focuses on overseeing clinical trials, where you will assure adherence to Good Clinical Practices and foster relationships with investigators. Your monitoring experience is essential to ensure all regulatory requirements are met. You’ll work closely with clinical teams to manage the study lifecycle from initiation to closeout.

Key Responsibilities:

• Monitor phases II-III clinical research studies
• Assure compliance with Good Clinical Practices
• Initiate and qualify investigator sites
• Supervise study conduct under regulatory guidelines
• Ensure integrity of study procedures and data

Requirements

• Bachelor's degree in life sciences required
• At least 1 year monitoring experience as CRA
• Familiarity with clinical studies and site management
• Strong English communication skills
• Clean driver's license required

Maximize your impact in clinical research by ensuring thorough oversight and compliance at every stage of the study.

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