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IQVIA Biotech is seeking a Clinical Research Associate (CRA) with experience in oncology solid tumor monitoring. The role requires at least 1 year of on-site monitoring experience, focusing on ensuring compliance with study protocols and regulatory standards to support successful clinical trials.
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Job Summary
IQVIA Biotech is a full-service CRO purpose-built to serve biotech sponsors with over 25 years of experience.
The role involves conducting all types of site visits including selection, initiation, monitoring, and close-out in alignment with GCP and ICH guidelines.
Candidates must have specific experience monitoring in oncology solid tumors to ensure the integrity and quality of clinical research data.
Matching Summary
Match Score: 75
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IQVIA Biotech is seeking a Clinical Research Associate (CRA) with experience in oncology solid tumor monitoring. The role requires at least 1 year of on-site monitoring experience, focusing on ensuring compliance with study protocols and regulatory standards to support successful clinical trials.
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Salary
Base: $71,900.00 - $169,300.00; Bonus/Equity: Incentive plans and bonuses may be offered; Benefits: Range of health and welfare benefits included
Skills & Requirements
Must-have
On-site monitoring experience
Oncology solid tumor monitoring
GCP and ICH guidelines knowledge
Nice-to-have
Agile therapeutically aligned solutions
Cross-functional project team collaboration
Strong communication skills
Key Requirements
Bachelor's degree in life sciences or health-related field
Minimum 1 year on-site monitoring experience for CRA 2
Minimum 6 months on-site monitoring experience for CRA 1 candidates