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CRA II

Warsaw
Permanent
Reference: JR071884
Description

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 Role

  • Working independently and actively to coordinate activities to set up and monitor a study, completing accurate study status reports and maintaining study documentation
  • Submission of protocol, consent documents for ethics/IRB approval and assist in preparing regulatory submissions as requested
  • Participate in preparing and reviewing study documentation and feasibility studies for new proposals as required
  • Balancing sponsor generated queries efficiently and responsible for study cost-effectiveness
  • Dependent 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

  • +2 years of monitoring experience as a CRA
  • Knowledge of ICG GCP guidelines and expertise to review and evaluate medical data
  • You will possess excellent written and verbal communication in English and Polish
  • Ability to produce accurate work to tight deadlines within a pressurized environment
  • You will be asked to travel at least 60% of the time (international and domestic -fly and drive) and should possess a valid driving license
 

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