Highly motivated and experienced Clinical Research Associate with robust background in conducting in-depth research and analysis and about 7 years of experience in clinical trial management, wet/dry laboratory work, site management and monitoring. Proven track record of successfully conducting site visits, managing investigator sites, and ensuring compliance with ICH-GCP regulations. Successfully contributed to multiple high-impact projects, delivering valuable insights and innovative solutions. Skilled in data collection/analysis/interpretation, statistical analysis, report writing, advanced methodologies, trial tools (CTMS, eTMF), EDC system and showcasing strong problem-solving/critical-thinking skills.
To secure an exciting Clinical Research Associate role, utilizing my skills and experience to ensure successful clinical trial management.
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