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Clinical Monitoring lead

Excelya · Paris, Île-De-France, FR

At Excelya, we embody Audacity, Care, and Energy in all that we do. We offer a dynamic and inclusive environment where innovation and collaboration drive suc...

Job description

About the Job At Excelya, we embody Audacity, Care, and Energy in all that we do. We offer a dynamic and inclusive environment where innovation and collaboration drive success. The Clinical Monitoring Lead will oversee and coordinate clinical monitoring activities to ensure the successful and compliant execution of clinical trials. This role involves leading CRA teams, ensuring quality standards are met, and maintaining effective communication with stakeholders to implement best clinical practices. Main Responsibilities: - Oversee and coordinate CRO clinical and site management activities throughout study start‑up, conduct, and close‑out phases. - Ensure efficient and high‑quality study start‑up by reviewing feasibility assessments, supporting site selection, and verifying the timely collection of essential regulatory and ethics documents prior to site initiation. - Support and ensure completion of sponsor‑specific clinical tasks within EDC, CTMS, and other study systems according to defined timelines. - Support CRO teams in CRA training on study‑specific operational activities and participate in the preparation and organization of investigator and monitor meetings. - Support Globa...