
This full-time Clinical Research Associate 2 role supports the Medical Device & Diagnostics team within a US-based organization. The position requires French language proficiency and involves leading site monitoring activities, including pre-study visits, routine oversight, and close-out procedures to ensure protocol adherence and data integrity. Key responsibilities also include managing serious adverse event reporting, coordinating with vendors, and assisting with the training of new staff. The role is appealing for its opportunity to work in a fast-paced, technology-driven environment that values teamwork and adaptability. While the position is designated as remote, it requires significant travel, estimated at 60-70% of the time, with frequent domestic and occasional international trips to clinical sites. The company offers a comprehensive benefits package and a culture focused on employee recognition and resource groups.





















