Senior Clinical Research Associate 100%

<p><strong>Key Responsibilities</strong></p> <ul> <li>Support the planning, coordination, and execution of clinical trials throughout all phases of the study lifecycle</li> <li>Contribute to feasibility assessments, site identification, and start-up activities including regulatory and ethics submissions</li> <li>Conduct on-site monitoring visits such as site initiation, routine monitoring, and close-out visits</li> <li>Ensure that clinical trials are conducted in compliance with study protocols, ICH-GCP guidelines, and applicable regulations</li> <li>Review and verify clinical data, source documents, and study records to ensure accuracy and completeness</li> <li>Prepare and maintain essential clinical documentation including monitoring reports and study-related correspondence</li> <li>Build and maintain strong relationships with investigational sites and external stakeholders</li> <li>Identify, track, and follow up on study-related issues, deviations, and corrective actions</li> <li>Coordinate site activities and support operational aspects of site management, including contracts and timelines</li> <li>Act as a key liaison between study sites, sponsors, and internal teams</li> <li>Support the preparation and submission of regulatory documentation and study updates where required</li> <li>Contribute to process improvements and ensure efficient study execution</li> </ul>