IQVIA Biotech is seeking an experienced Clinical Research Associate to perform site monitoring visits, drive patient recruitment plans and ensure regulatory compliance for oncology studies. The role involves authoring visit reports, coordinating with sites and internal teams, and maintaining TMF/ISF documentation.
Strong English communication and timely issue escalation are essential. Minimum 3–4 years of on-site monitoring experience and a Bachelor’s degree in a scientific field or healthcare
Senior Oncology CRA - Site Monitoring & Study Leadership in Sefton 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.
