/ http://www.slideshare.net/images/logo.gif / 際際滷Share feed for 際際滷shows by User: drshrikantdesai https://cdn.slidesharecdn.com/profile-photo-drshrikantdesai-48x48.jpg?cb=1713596190 * Complete understanding of scientific rudiments and principles of Controlled Clinical Trials methodology and process * Practical hands on experience in phase III Oncology, Nephrology, General Medicine and General Surgery trials. * Good clinical knowledge and exposure to medical terminology, medications, and pharmacology. * Practical knowledge on ICH / GCP guidelines; Schedule Y; Ethical principles; US FDA and European Union regulatory requirements. * Experience in designing and developing contracts, agreements, SOPs, site files, trial master files, CRFs, study-specific logs, guidelines, manuals and reports. * Capacity to plan and carry out pre-study, initiation, routine monitoring and c...