in training and mentoring less expert CRA’s and/or lead CRA’s working on international projects What monitoring experience in phase I-III trials as a CRA Knowledge of ICG GCP guidelines and expertise to
Senior CRA Client Dedicated Homebased ICON plc is a world-leading healthcare intelligence and clinical in training and mentoring less expert CRA's and/or lead CRA's working on international projects To be monitoring experience in phase I-III trials as a CRA Knowledge of ICG GCP guidelines and expertise to
in training and mentoring less expert CRA's and/or lead CRA's working on international projectsWhat you monitoring experience in phase I-III trials as a CRA Knowledge of ICG GCP guidelines and expertise to
development. ICON South Africa is seeking an experienced CRA in Gauteng, to join one of our largest embedded sponsor opportunities. As a Clinical Research Associate (CRA) you will coordinate all aspects of the clinical
risks. This role is also accountable for identifying CRA performance issues and is responsible for ensuring Assurance (preferred) Site Management/Monitoring (CRA) experience (preferred) Project management experience
Trial Lead/Manager Prior monitoring experience as a CRA is preferred Ability to travel up to 20% Fluent in
related processes Requirements Knowledge of the NCA, CRA, FAIS, FICA; 3 years experience in a similar role
years´ experience in a functional management position CRA , project management and CRM experience Line management
completion of compliance risk and control assessments (CRA's) Ensure that compliance risk is adequately identified