CRA I

As a Clinical Research Associate I 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 RoleWorking independently and actively to coordinate activities to set up and monitor a study, completing accurate study status reports and maintaining study documentationSubmission of protocol, consent documents for ethics/IRB approval and assist in preparing regulatory submissions as requestedParticipate in preparing and reviewing study documentation and feasibility studies for new proposals as requiredBalancing sponsor generated queries efficiently and responsible for study cost-effectivenessDependent on level of experience you may assist in training and mentoring less expert CRA's and/or lead CRA's working on international projects

What you need+1 years of monitoring experience as a CRAKnowledge of ICG GCP guidelines and expertise to review and evaluate medical dataYou will possess excellent written and verbal communication in EnglishAbility to produce accurate work to tight deadlines within a pressurized environmentYou will be asked to travel at least 60% of the time (international and domestic -fly and drive) and should possess a valid driving license