ROLE REQUIREMENTS 2+yrs home based clinical monitoring experience (CRO or Sponsor) Familiarity with appropriate EU Pharmaceutical legislation e.g. ...
Successfully developing e-trading solutions that meet sponsor/stakeholder needs
while demonstrating high levels of quality and productivity. ...
ROLE To conduct pre-study, initiation,
monitoring and closeout visits for sponsored clinical studies in compliance with QCTR /Sponsor ICH GCP ...
Unique opportunity for an experienced CRA to move into role for one of the worlds foremost CROs globally they are one of the top 5 providers of ...
Facilitates the appointment of project managers to the
project delivery teams -Reporting progress of the programme at regular intervals to the ...