Medical Doctor with a decade of clinical experience, adept in clinical research methodologies and protocols. Seeking to leverage expertise in data management, informed consent procedures, and comprehensive understanding of Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) regulations into a rewarding role in clinical research. Proven ability in clinical monitoring and a track record of ensuring adherence to regulatory standards. Adept at analyzing complex data sets and identifying opportunities to enhance the quality of clinical research initiatives.
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