Highly motivated biochemistry graduate with a post-grad diploma in clinical research, pharmacovigilance, and regulatory affairs seeking a challenging role as a Clinical Research Associate (CRA). Passionate about making a positive impact through research and eager to contribute to the advancement of clinical trials. SUMMARY OF QUALIFICATIONS Demonstrated Adapted strategies to optimize work during the pandemic with minimal supervision Skilled in analyzing complex information, drawing logical conclusions, and offering creative alternatives. Training in International Conference on Harmonization – Good Clinical Practice Guidelines (ICH-GCP) and Health Canada Division 5. Knowledgeable in clinical monitoring practices, including site management, protocol compliance, and data quality assurance. Acquired strong academic foundation in medical records through coursework in health information management, data privacy, and electronic health records.