IQVIA Biotech is recruiting for an on-site Clinical Monitor in the United Kingdom. You will conduct site visits from initiation to close-out, ensure compliance with GCP/ICH, and support recruitment planning and regulatory submissions for oncology studies.
Strong communication and organizational skills are essential. Ideal candidates have at least 1 year of on-site monitoring experience, a scientific/healthcare degree, and proficiency with MS Office.
Oncology Clinical Research Associate — Site 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.
