Found Description
You will be joining a program takes an extensive co-monitoring approach that enables a supportive and collaborative work environment. Frequent, consistent communication, both internally and with our client, positions our program to be closely aligned on our shared goals.
**What you will be doing**:
- Act as an expert advisor on ICH GCP, ICON SOPs/WPs and all stages of study set-up, monitoring and study close-out for less experienced colleagues. Provide a benchmark of monitoring competence to inexperienced/less experienced colleagues
- Become involved, when required, in other areas of study management and staff training and contribute to the review of ICON systems and procedures as appropriate
- Identify, select, initiate, and close-out appropriate investigational sites for clinical studies. Monitor those sites in order to ensure that studies are carried out according to the study protocol, ICON SOPs/WPs, applicable regulations and the principles of ICH-GCP
**You are**:
**What you will be doing**:
- Act as an expert advisor on ICH GCP, ICON SOPs/WPs and all stages of study set-up, monitoring and study close-out for less experienced colleagues. Provide a benchmark of monitoring competence to inexperienced/less experienced colleagues
- Become involved, when required, in other areas of study management and staff training and contribute to the review of ICON systems and procedures as appropriate
- Identify, select, initiate, and close-out appropriate investigational sites for clinical studies. Monitor those sites in order to ensure that studies are carried out according to the study protocol, ICON SOPs/WPs, applicable regulations and the principles of ICH-GCP
**You are**: