Precision for Medicine is not your typical CRO. We integrate clinical trial execution with deep scientific knowledge, laboratory expertise, and advanced data sciences to expedite the development of life-changing therapies. Our strong focus on Oncology and Rare Disease sets us apart. We take pride in our exceptional CRA retention rates, fostering a culture where employees thrive and enjoy a balanced work-life. As a Clinical Research Associate II, you will have a manageable number of protocols, allowing you to become a protocol expert while enjoying reasonable travel commitments.

You will be responsible for monitoring and managing the progress of clinical studies at investigative sites, ensuring compliance with protocols, SOPs, ICH-GCP, and applicable regulations. Your tasks will include coordinating all necessary activities for study setup and monitoring, such as identifying investigators and preparing for regulatory submissions.