The CRA will conduct site visits (i.e., PSSV, SIV, IMV, COV) and function as the site manager, building and maintaining relationships with key site personnel
Job Summary
The CRA will conduct site visits (i.e., PSSV, SIV, IMV, COV) and function as the site manager, building and maintaining relationships with key site personnel.
CRAs are responsible for monitoring data quality and patient safety through monitoring and site education, ensuring compliance with ICH-GCP guidelines, local regulations, and SOPs.
This role involves mentoring less experienced CRAs, providing audit/inspection preparation support, and collaborating with the Clinical Study Team to ensure timely delivery of study milestones.
Matching Summary
The CRA will conduct site visits (i.e., PSSV, SIV, IMV, COV) and function as the site manager, building and maintaining relationships with key site personnel.
Skills & Requirements
Must-have
ICH-GCP guidelines
site visits
data quality monitoring
patient safety monitoring
Fluent English required
Nice-to-have
collaborative spirit
fighting cancer
Spanish is a plus
Hematology
Oncology
Key Requirements
BS/BA in a relevant scientific discipline
minimum of 3+ years of Clinical Operations experience