We are seeking an experienced **Clinical Research Associate** , fully sponsor-dedicated, with a strong background in **oncology trials** . This is an excellent opportunity to advance your career within a **leading global CRO** , where you’ll work in a **stable, supportive, and international environment** that values quality and professional growth.
**Your responsibilities will include:**
+ Performing site selection, initiation, monitoring and close-out visits + Supporting the development of a subject recruitment plan + Evaluating the quality and integrity of site practices in accordance with regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines + Managing progress by tracking regulatory submissions, recruitment, case report form (CRF) completion, and data query resolution + Collaborating with experts at study sites and with client representatives