Clinical Research Associate I

Precision for Medicine, Oncology and Rare Disease is not your typical CRO. We are hiring a proactive Clinical Research Associate I to join our team in Poland. As a CRA, you will focus on an average of one to two studies setting you up to be a protocol expert and your voice will be heard. You will monitor and own the progress of clinical studies at investigative sites and ensure that clinical studies are conducted, recorded, and reported per protocol, SOPs, ICH-GCP, and all applicable regulations and standards. You will coordinate all necessary activities required to set up and monitor a study (i.e., identify investigators; helping prepare regulatory submissions, conducting pre-study and initiation visits, etc.).