Senior Oncology CRA - Frontline Clinical Trial Monitoring
IQVIA Biotech is seeking an experienced Clinical Research Associate to perform on-site monitoring for oncology studies. You will ensure GCP/ICH compliance, manage regulatory submissions, and support site coordination to drive patient recruitment and data integrity.
The role requires 3–4 years of monitoring experience, strong English communication, and proficiency with MS Office. A bachelor’s degree in a scientific field is preferred; visa sponsorship is not offered.
Join us at IQVIA LLC as our next Senior Oncology CRA
- Frontline Clinical Trial Monitoring in England, United Kingdom.
Join IQVIA LLC and contribute to our ongoing work.
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This posting is for the Senior Oncology CRA
- Frontline Clinical Trial Monitoring role at IQVIA LLC, based in England, United Kingdom.
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