Senior Clinical Research Associate

Job Summary

A company is looking for a Senior CRA.

Key Responsibilities

• Manage investigator site activities and ensure compliance with clinical trial protocols and regulations
• Serve as the primary contact for assigned sites, facilitating communication and addressing operational issues
• Conduct monitoring visits, submit required documentation, and resolve site-related issues in a timely manner

Required Qualifications

• Bachelor's degree in life sciences or equivalent professional degree
• Minimum of 3 years of experience in clinical research site monitoring
• Extensive knowledge of clinical trial methodologies and regulations (ICH/GCP, FDA)
• Preferred therapeutic experience in Vaccines, Internal Medicine, or Infectious Diseases
• Fluency in English and the native language of the country of work