Senior Oncology Clinical Research Associate - 164596

Responsibilities: for the Senior Contract Oncology Clinical Research Associate: Conduct site and study visits and perform all site monitoring activities across multiple study Responsible for both remote and on-site monitoring and study activation Participate in the development of study tools, protocols, and clinical trial documentation Some travel required once travel bands are lifted Qualifications: for the Senior Contract Oncology Clinical Research Associate: 6+ years of Oncology on-site Monitoring and hands on experience with EDC Systems Experience with on-site Oncology monitoring is non-negotiable Organization to perform monitoring duties across multiple sites is a must.