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.
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Senior Oncology CRA - Frontline Clinical Trial Monitoring employer: IQVIA LLC
At IQVIA, we pride ourselves on being an exceptional employer, particularly for those in the field of Pharmaceutical Development. Our Cambridge location fosters a collaborative and innovative work culture, where you will have the opportunity to influence scientific direction, mentor junior scientists, and engage directly with clients. With a strong focus on employee growth and the integration of cutting-edge AI-enabled approaches, we are committed to supporting your professional development while making a meaningful impact in the pharmaceutical industry.
