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Senior CRA Oncology

Chiltern

Milan, Italy

Duties & Responsibilities

  • Perform all types of site visits (qualification visits, initiation visits, monitoring visits, motivational visits, audit support visits, and close-out visits);
  • Identify potential sites in collaboration with the Project Team, and conduct feasibility assessment of sites as required;
  • Ensure that all study related communication is tracked, printed and filed as required;
  • Follow-up and track patient recruitment by contacting investigators and escalate potential risks and opportunities with the Project Manager and/or LCRA;
  • To assemble files and ensure documents for the trial master file accurately reflect the progress of the study.

Requirements

  • Graduate or Post-graduate Scientific educational background;
  • Previous CRA experience within clinical research, preferably in CRO or Pharma companies of approximately 3 years minimum, expertise in oncology required;
  • Good clinical knowledge and good understanding of medical terminology;
  • Good ICH GCP knowledge and good understanding of regulatory requirements;
  • Experience as a CRA on multicenter trials;
  • Good oral and written communication, organizational skills and personal presentation;
  • The ability to communicate effectively in Dutch and English;
  • Good computer literacy with working knowledge of PCs, Windows and Microsoft Office applications.

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