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CRA II, home based
ICON Public Limited Corporation
As a global provider of drug development solutions, our work is serious business. But that doesn't mean you can't have fun while you do it...
As a global provider of drug development solutions, our work is serious business. But that doesn't mean you can't have fun while you do it. With our vision to be the partner of choice in drug development, we hire only the best and brightest in the industry. Are you one of them?
As a Clinical Research Associate at ICON, you'll work within a large-scale, fast-paced environment alongside a close-knit team of highly qualified CRAs to identify, select, initiate and close-out investigational sites for clinical studies in phases II - IV, ensuring adherence to applicable regulations and principles of ICH-GCP. We pride ourselves on our amazing company culture, where we work as one team to achieve industry-leading results.
The roleIndependent, proactive work to set up and monitor studies, complete reports and maintain documentationSubmitting protocol, consent documents for ethics/IRB approval, as well as preparing regulatory submissionsManaging sponsor generated queriesTaking responsibility for study cost effectivenessPreparation and review of study documentation and feasibility studies for new proposalsPotential to assist in training and mentoring fellow CRAs
What you needUniversity degree in medicine, science, or equivalentPrevious monitoring experience in medium sized studies, including study start-up and close-outKnowledge of ICH-GCP guidelines and ability to review and evaluate medical dataExcellent written and verbal communication in Portugese and EnglishAbility to work to tight deadlinesAvailability to travel at least 60% of the time
Job posted: 2020-11-27
