Clinical Site Activation Specialist
ICON plc is seeking a Site Activation Partner to support study site activation and regulatory submissions. You will coordinate IRB and regulatory documents and liaise with SRPs and Study Start Up teams. The role requires strong organizational and communication skills, with at least two years in clinical site management.
You will work across English documentation and French where applicable. This position offers exposure to global trials in a fast-paced environment with focus on timely
This posting is for the Clinical Site Activation Specialist role at ICON Strategic Solutions, based in Canada.
The following opening is for a Clinical Site Activation Specialist with ICON Strategic Solutions.
Our group is growing, and we are hiring a Clinical Site Activation Specialist in Canada.
This opening is for the Clinical Site Activation Specialist role at ICON Strategic Solutions.
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