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.
Independent, proactive work to set up and monitor studies, complete reports and maintain documentation
Submitting protocol, consent documents for ethics / IRB approval, as well as preparing regulatory submissions
Managing sponsor generated queries
Taking responsibility for study cost effectiveness
Preparation and review of study documentation and feasibility studies for new proposals
Potential to assist in training and mentoring fellow CRAs
What you need
University degree in medicine, science, or equivalent
Previous monitoring experience in medium sized studies, including study start-up and close-out
Knowledge of ICH-GCP guidelines and ability to review and evaluate medical data
Excellent written and verbal communication in German and English
Ability to work to tight deadlines
Availability to travel at least 60% of the time