Clinical Research Associate for Regulatory Compliant Trials

Elevate your clinical research career as a Clinical Research Associate! Manage and monitor studies in phases II and III while ensuring compliance and integrity throughout the study lifecycle. In this pivotal role, you'll focus on overseeing clinical studies, maintaining adherence to GCP, and building robust relationships with investigators.

Your responsibilities will include the qualification and initiation of study sites, alongside supervising the study conduct to ensure regulatory compliance.

Your role is vital to the success of clinical research initiatives. Key Responsibilities:

• Oversee monitoring of clinical studies in phases II-III
• Ensure compliance with Good Clinical Practices
• Identify and initiate investigators and their sites
• Supervise study conduct in line with regulations
• Manage adherence to study procedures and integrity Requirements:
• Bachelor's degree in life sciences
• Minimum 1 year of CRA experience in relevant settings
• Experienced in site initiation and close-out processes
• Clinical study experience in phases II-III
• Excellent English communication proficiency Bring your expertise in monitoring and compliance to advance clinical research and support innovative treatments.