We are partnered with a growing company that is seeking a Senior Clinical Research Associate. The Senior Clinical Research Associate is responsible for the overall management and oversight of assigned clinical trial sites, including site identification, feasibility assessments, pre-study evaluations, study start-up, site initiation, patient recruitment, site monitoring, close-out activities, inspection readiness, and local regulatory and IRB/EC submissions. This role ensures clinical studies are conducted in accordance with study protocols, Standard Operating Procedures (SOPs), ICH-GCP guidelines, and all applicable regulatory requirements while supporting the successful execution of clinical programs. Responsibilities: Oversee the successful start-up, monitoring, and execution of Phase I–IV clinical studies at assigned investigative sites. Conduct clinical site management and monitoring activities in compliance with ICH-GCP guidelines, Standard Operating Procedures (SOPs), study proto...