
ICON Clinical Research
As a worldwide supplier of drug improvement options, our work is severe enterprise. But that does not imply you may’t have enjoyable when you do it. With our imaginative and prescient to be the accomplice of selection in drug improvement, we rent solely the very best and brightest within the {industry}. Are you one in every of them?Please make an utility promptly if you’re a very good match for this position attributable to excessive ranges of curiosity.As a Clinical Research Associate at ICON, you will work inside a large-scale, fast-paced surroundings alongside a close-knit workforce of extremely certified CRAs to establish, choose, provoke and close-out investigational websites for medical research in phases II – IV, making certain adherence to relevant rules and rules of ICH-GCP. We delight ourselves on our wonderful firm tradition, the place we work as one workforce to attain industry-leading outcomes.*The position** Independent, proactive work to arrange and monitor research, full reviews and keep documentation* Submitting protocol, consent paperwork for ethics/IRB approval, in addition to getting ready regulatory submissions* Managing sponsor generated queries* Taking duty for research value effectiveness* Preparation and assessment of research documentation and feasibility research for brand spanking new proposals* Potential to help in coaching and mentoring fellow CRAs*What you want** University diploma in drugs, science, or equal* Previous monitoring expertise in medium sized research, together with research start-up and close-out* Knowledge of ICH-GCP pointers and talent to assessment and consider medical knowledge* Excellent written and verbal communication in Dutch and English* Ability to work to tight deadlines* Availability to journey at the very least 60% of the time
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