IQVIA is seeking a Clinical Research Associate to support Oncology studies across the UK. You will perform on-site monitoring visits, ensure protocol training, and maintain open lines of communication with sites to manage expectations and issues.
Responsibilities include tracking regulatory submissions, recruitment progress, CRF completion, and TMF/ISF filing while upholding GCP and ICH standards. Travel to sites will be required as needed.
#J-18808-Ljbffr
Oncology CRA – UK Site Monitoring & Impact in Manchester 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.
