Senior Clinical Research Associate

Job Summary

A company is looking for a Senior CRA to manage and monitor clinical trial sites.

Key Responsibilities

• Oversee investigator site management and ensure compliance with clinical trial protocols and regulations
• Serve as the primary contact for assigned sites, facilitating communication and resolving issues
• Conduct monitoring activities, including site initiation, routine monitoring, and close-out, while ensuring timely reporting and documentation

Required Qualifications

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