Clinical Research Associate

📋 Description

• Build trusted and effective partnerships with investigators and site staff by aligning them with
• Conduct site qualification, site initiation, routine on-site and remote monitoring, and study
• Train site personnel on the protocol, study procedures, safety reporting requirements, and relevant
• Oversee site activities, proactively identify risks and compliance issues, and support the
• Ensure the quality and timely submission of data from investigative sites, including appropriate
• Support patient recruitment and retention activities by applying an understanding of the patient

🎯 Requirements

• Bachelor’s degree or equivalent qualification in a health-related or scientific discipline
• Minimum of one year in clinical research monitoring.
• Strong planning, organizational, communication, and interpersonal skills, with the ability to
• Good analytical and problem-solving skills, with the ability to identify site issues, exercise
• Self-motivated and collaborative, with a strong commitment to quality, compliance, patient safety