Job Description
As a Senior Clinical Scientist you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. Senior Clinical Scientist will support late phase development in oncology area, this role is dedicated to a global biotech company. Responsibilities include contributing to the development and creation of clinical trial protocols following high scientific and clinical standards and applicable regulations. Also contribute to the identification, formulation and implementation of amendments to the clinical protocol, in close collaboration with clinical lead. The candidate will contribute to the creation of study-level documents, including preparation of clinical sections of key regulatory documents, such as Investigator’s Brochures, briefing books, safety updates and submission dossiers. Support regulatory activities, like preparation of meetings with regulatory agencies. Perform high quality clinical data review and identify clinical data insights through ongoing patient level review and trends analysis, thereby supporting Interim Analysis, Database and Post Lock activities and resolution of scientific & medical issues throughout the study lifecycle.
About ICON
ICON is the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.