Sarthak Bhardwaj

 I am a dedicated Clinical Research Coordinator and Data Manager with over two years of experience supporting the successful delivery of multi-phase clinical trials across oncology, academic, and multidisciplinary healthcare settings. With a strong foundation in Good Clinical Practice (GCP), regulatory compliance, and clinical governance, I specialize in coordinating trial logistics, managing case report forms (CRFs), and ensuring the accuracy and integrity of clinical data.

My expertise includes patient recruitment, ethics submissions, adverse event reporting, and cross-functional collaboration with investigators, Clinical Trials Units (CTUs), and sponsor monitors. I am adept at using clinical databases and trial management systems to streamline documentation, support audit readiness, and maintain high standards of data quality throughout the research lifecycle.

Currently pursuing the CAPM certification by PMI, I combine research acumen with emerging project management capabilities, aiming to bridge the gap between clinical operations and strategic execution. Passionate about innovation in healthcare, I am committed to contributing to evidence-based practice through ethical, efficient, and patient-centered research.