ARTI CHIDE

Clinical Research professional with hands-on experience as a Clinical Research Coordinator, skilled in clinical trial management, remote monitoring support, and regulatory compliance. Proficient in Clinion, OctelSoft, and CodeAngilo systems with strong knowledge of GCP, ICMR guidelines, and NDCT rules. Experienced in site coordination, data review, query resolution, and maintaining high-quality trial documentation. Possess foundational preclinical knowledge including animal handling, toxicity studies, OECD guidelines, 3Rs principles, and GLP. Detail-oriented with strong analytical and coordination skills, aiming to contribute effectively in CRA, Centralized Monitoring, and CTA roles. Currently pursuing Masters in Pharmacology and Toxicology.

• Certified in NIDA Clinical Trials Program, strengthening knowledge in clinical research and regulatory practices
• Completed Clinical Trials Training (15 days) with hands-on exposure to study processes and documentation
• Participated in National-Level Pharma Quiz Competition, demonstrating strong subject knowledge
• Presented research at Institute-Level Poster Presentation and participated in Avishkar Competition
• Attended International and National Conferences to enhance knowledge of current trends.
• Completed Diploma in Computer Applications (DCA) and CCC Certification, with proficiency in computer systems and data handling