
As a detail-oriented healthcare professional with training in Good Clinical Practice (GCP) and clinical research processes, I am eager to contribute to your organization in an administrative or clinical research capacity. With a strong foundation in compliance, documentation, patient coordination, and data management, I am committed to building on my skills while helping the organization achieve its goals. I am particularly interested in an entry-level role such as Clinical Research Assistant, Clinical Trial Assistant, or Regulatory Coordinator, where I can continue to develop my expertise in clinical studies and make a positive impact. Through my work, I aim to support the success of your team and fulfill my passion for helping others."