The CRA will conduct site visits, function as the site manager, and build/maintain relationships with key site personnel to ensure effective communication
Job Summary
The CRA will conduct site visits, function as the site manager, and build/maintain relationships with key site personnel to ensure effective communication.
CRAs are responsible for monitoring data quality and patient safety through monitoring and site education, adhering to ICH-GCP guidelines and SOPs.
This role involves mentoring less experienced CRAs, tracking site performance metrics, and collaborating with the Clinical Study Team to ensure timely delivery of study milestones.
Matching Summary
The CRA will conduct site visits, function as the site manager, and build/maintain relationships with key site personnel to ensure effective communication.
Skills & Requirements
Must-have
ICH-GCP guidelines
site visits (PSSV, SIV, IMV, COV)
data quality and patient safety monitoring
Fluent English required
Hematology, Oncology experience
Nice-to-have
collaborative and motivated professionals
passionate interest in fighting cancer
Spanish is a plus
Entrepreneurial Mindset
Continuous Learning
Key Requirements
BS/BA in relevant scientific discipline
minimum of 3+ years Clinical Operations experience