Kavitha Vittal

Background

About Kavitha Vittal

Clinical scientist/Medical monitor on oncology trials experienced in protocol design and implementation, trends and outlier review, aggregate medical data review, imaging, protocol deviation, regulatory document review and medical monitoring. Skilled in the review of clinical trial data pertaining to drugs, devices and vaccines. Good knowledge of good clinical practices (GCP), regulatory guidelines and health Canada FDA and EMA standards and guidelines. Reliable and a team-player and deliver work accurately and on time. As a Medical Data Reviewer (MDR), conducted in-stream data trend analysis in support of data quality and integrity for several therapeutic areas. Reviewed inclusion and exclusion criteria, clinical trial information and coding reports for accuracy and consistency, summary reports, medical monitoring plans and other relevant study-related documents. Proficient in Database tools such as Medidata rave/iMedidata and Inform. As a dentist and academician, I’ve examined, diagnosed and treated my patients with compassion. Children's stories, editorials and scientific writing are my other passions Any work allocated to me is delivered with precision and creativity.