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
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