Contributor to routine, consolidated Study Monitoring updates
Perform all aspects of CRA duties from site selection, site initiation, through to site routine monitoring visits through to close-out visits and database lock.
You will be embedded in our client's study team and have a dedicated ICON line manager to support you
Oversees all aspects of study site management to ensure high quality data resulting in consistently low query levels and in good Quality Assurance reports
Qualifications
Degree in Pharmacy or any related course
2+ years prior monitoring experience with global trials at CRO/ pharmaceutical or Biotechnology company, preferrrably within oncology monitoring experience
Excellent Thai & English communication skills
Passion to contribute to developing Cancer treatment
Excellent knowledge of international guidelines ICH-GCP, good knowledge of local regulations
