California Licensed Clinical Research Associate

Job Summary

A company is looking for a Sr. Clinical Research Associate (Temporary).

Key Responsibilities

• Support site management activities including identification, qualification, and monitoring
• Conduct site monitoring visits to ensure compliance with study protocols and regulatory requirements
• Track regulatory document submissions and assist in the development of study documents

Required Qualifications

• Bachelor's degree in Life Sciences, Nursing, or a related field
• Minimum of 4-6 years of experience in clinical research, including IVD experience
• Experience with site monitoring and understanding of clinical trial processes
• Proficiency with EDC systems, CTMS, and eTMF
• Ability to work independently and collaboratively in a fast-paced environment