Job Description - California Licensed Clinical Research Associate
A company is looking for a Sr. Clinical Research Associate.
Key Responsibilities
Support site management activities including identification, qualification, and monitoring of clinical sites
Conduct site monitoring visits to ensure compliance with study protocols and regulatory requirements
Track regulatory document submissions and ensure audit-readiness of essential documents
Required Qualifications
Bachelor?s degree in Life Sciences, Nursing, or a related field
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 dynamic environment
