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
• Conduct monitoring visits and provide training and support to site personnel
• Resolve site issues and ensure timely submission of required documentation and reports

Required Qualifications

• Bachelor's degree in life sciences or a related professional field
• Minimum of 3 years of experience in clinical research site monitoring
• Extensive knowledge of clinical trial methodologies and regulatory requirements
• Preferred experience in Vaccines, Internal Medicine, or Infectious Diseases
• Fluency in English and the native language(s) of the country of work