Clinical Research Associate

Position:  Clinical Research Associate
Department: Accord Research (SOTIO/PPF Group)
Location: Prague, Czech Republic
Employment Type: Full time employment

 

Position Summary

Responsible for recruitment of potential investigators, involvement in CA and EC submissions and notifications to regulatory authorities, translation of study-related documentation, organization of meetings and other tasks as instructed by supervisor. Responsible for monitoring of clinical sites, maintenance of study files, conduct of pre-study and initiation visits, liaison with vendors and other duties. Functions as the primary contact for sites regarding regulatory compliance and protocol questions and communicates with clinical sites on an ongoing basis to address and resolve issues. May be required to train, coach and supervise junior staff. 

We require

  • Excellent knowledge of the clinical trial process and ICH/GCP guidelines;
  • Ability to coach and mentor other clinical staff;
  • Excellent organizational and time management skills to handle multiple priorities;
  • Excellent written and oral communication skills;
  • Fluent in written and verbal English;
  • Computer competency;
  • At least 2 years of experience in monitoring and organization of clinical trials;
  • University or college degree; life sciences preferable or certification in a related allied health profession (e.g. nursing certification, medical or laboratory technology).

Contact us

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