Clinical Study Manager
... world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. What you will be doing: Has the overall responsibility for the study commitments within the country and ...
... world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. What you will be doing: Has the overall responsibility for the study commitments within the country and ...
... Clinical Trial Site Relationship Coordinator to join our vibrant Clinical ... excels in delivering innovative research and development of cutting edge ... and or therapeutic areas, and study start-up; Proactively research and understand specified site landscape ...
... as coordination and tracking of study materials and equipment Ø Assist in ... for the duration of the study Ø Set-up and maintenance of ... the eTMF “Inspection Readiness” and study documents are ready for final ...
... a leader of the Study Start-up team you will ... in other facets of Study Start-up are welcome. Responsibilities ... operating procedures and study protocols; Provide input on new ... full-service clinical contract research organization (CRO). We provide Phase ...
... are currently seeking a Feasibility Coordinator, who will be a member ... therapeutic and operational experience Create study-specific feasibility questionnaires, cover letters, ... a full-service clinical contract research organization (CRO). We provide Phase ...
... career in the research and development of cutting-edge ... and collaborate on global study activities; working closely with the project coordinator and clinical trial manager Ensure ... -service clinical contract research organization (CRO). We provide Phase ...
... career in the research and development of cutting-edge ... and collaborate on global study activities; working closely with the project coordinator and clinical trial manager Ensure ... -service clinical contract research organization (CRO). We provide Phase ...
... development. As a Clinical Research Associate II at ICON, you’ll ... queries Taking responsibility for study cost efficiency Preparation and review of study documentation and feasibility studies for ... medium-sized studies, including study start-up and close-out ...
... world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. ... assigned region during the study start up period Building relationships ... Leading the preparation of study level essential document templates Aiding ...
... documentation, including protocols and clinical study reports Your Profile: Bachelors degree in a scientific or healthcare-related field. Minimum of 2 years of experience as a Clinical Research Associate. In-depth knowledge of ...