M.Pharm Pharmacology graduate with hands-on research experience in study execution, data handling, and scientific documentation, seeking to build a career in Clinical Research, Clinical Data Management, and Pharmacovigilance. Trained in Good Clinical Practice (GCP) and ICH Guidelines, with a working understanding of clinical trial fundamentals, protocol and SOP adherence, regulatory compliance, and drug safety principles. Skilled in data review, data interpretation, and clinical and research documentation, with a consistent focus on accuracy and quality within structured research environments. Effective in cross-functional settings, with strong attention to detail and a collaborative approach to research operations.
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