<ul><li>Oversee and monitor clinical trials to ensure compliance with regulatory guidelines and protocol.</li><li>Coordinate with clinical sites, ensuring proper implementation of research studies and recruitment of participants.</li><li>Review patient data, ensuring accuracy and integrity of clinical trial results.</li><li>Prepare and submit regulatory documents to ethics committees and health authorities.</li><li>Perform site initiation, monitoring, and close-out visits, ensuring proper documentation and reporting.</li><li>Collaborate with cross-functional teams to ensure timely delivery of project milestones.</li><li>Analyze and report on clinical trial progress, identifying and resolving any issues or discrepancies.</li><li>Ensure the safety and well-being of trial participants through ongoing assessments.</li><li>Stay updated on industry trends, guidelines, and best practices related to clinical research.</li></ul>

Clinical Research Associate