Quality oriented clinical trials specialist, with 7 years of experience in independent monitoring of clinical trials and 1 year experience as Feasibility Site Liaison Spec. Worked on clinical trials of phase II, III, IV in a variety of indications: Cardiology/Vascular Diseases, Oncology/Haematology, Respiratory Diseases, Neuroscience, Rare Diseases, General Medicine, Pediatric studies. Performed visits: pre-study, initiation, interim monitoring (with 100% or reduced SDV), close-outs. Supported interim analysis and database locks. Audited by sponsors. Demonstrates analytical thinking, ability to effectively communicate with cross-functional teams and problem-solving approach. Holds Ph.D. in Biochemistry.