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Régió: Budapest

HAYS Hungary Kft.
Hozzáadva: 2016.01.14.
Jelentkezési határidő: 2016.01.27.
Hirdetés azonosító: 1001121


Our small-sized CRO partner is urgently looking for a CRA to join their young and talented monitoring team in Budapest. They are open for both permanent employee/contractor status and you can be either office/home-based.

Your responsibilities will be:

  • Identify, select, initiate and close-out investigational sites for clinical studies in phases II – IV ensuring that applicable regulations and principles of ICG-GCP are adhered to
  • Coordinate all necessary activities required 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
  • Preparing and reviewing study documentation and feasibility studies for new proposals as required
  • Managing sponsor generated queries efficiently and responsible for study cost effectiveness
  • You may assist in mentoring junior CRA’s 
  • You will be involved in study design/medical writing projects as well

Your background should include:

  • Medical, pharmacist or other life-science degree
  • 1 to 3 years' monitoring experience preferably in a complex study
  • Knowledge of ICG GCP guidelines and expertise to review and evaluate medical data
  • Fluency in English
  • Excellent communication and interpersonal skills
  • Computer literate with Microsoft Office

Should you be interested do not hesitate to submit your application via our website.

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