A company is looking for a Clinical Research Associate II - Temporary.
Key Responsibilities
Conduct site initiation, routine monitoring, and closeout visits to ensure adherence to protocols and regulatory requirements
Perform source data verification, data collection, and query resolution to ensure accurate study data
Maintain and manage study documentation, including regulatory documents and trial master files
Required Qualifications
Bachelor's Degree
A minimum of 1-2 years of experience as a CRA or in a similar role
Strong understanding of clinical trial processes, regulations, and guidelines
CRA certification is a plus
Clinical Research Associate • Boca Raton, Florida, United States