Highly skilled Medical Reviewer with 2+ years of experience reviewing and editing clinical documents for the pharmaceutical and clinical product industry. Published writer with proven expertise in reviewing and editing various medical and scientific documents, including clinical study reports,manuscripts, and regulatory submissions. Proficient in regulatory guidelines, ICH GCP, and clinical development processes. Proficient in consistently delivering meticulously reviewed documents within specified timeframes. Adept at enhancing efficiency within document delivery department. Skilled at developing reports, analyzing data, and identifying solutions. Can handle responsibility individually and work well in a team. Willing to relocate and available to join immediately.