Clinical Research Associate I/ Clinical Research Associate II

📋 Description

• • As a Clinical Research Associate I/II at Precision Medicine Group, you will play a critical role in advancing oncology and rare disease clinical trials by ensuring studies are conducted in full compliance with protocols, SOPs, ICH-GCP, and regulatory standards.
• • Your day-to-day responsibilities include monitoring clinical study progress at investigative sites, coordinating site setup activities (such as identifying investigators and preparing regulatory submissions), conducting pre-study and initiation visits, and ensuring accurate data collection and reporting.
• • You will join a mission-driven, employee-focused CRO known for exceptionally high CRA retention, where your voice is valued, work-life balance is supported through reasonable travel, and you receive direct mentorship from engaged leadership.
• • This role offers the opportunity to become a protocol expert on one to two studies, develop deep expertise in oncology monitoring, and grow professionally in a collaborative environment that values initiative, problem-solving, and ownership of quality outcomes.