Overview
ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organisations. With our patients at the centre of all that we do, we help to accelerate the development of drugs and devices that save lives and improve quality of life. Our people are our greatest strength, are at the core of our culture, and the driving force behind our success. ICON people have a mission to succeed and a passion that ensures what we do, we do well.
Responsibilities
What will you be doing?
As a Country Lead Monitor, you are accountable and responsible for overall country clinical trial activities in assigned studies. The CLM oversees the CRAs and overall study progress for assigned studies within his/her country from country feasibility assessment through to study archive. The CLM manages the Country Feasibility process, involving local Monitoring and Site Management (MSM) personnel and local Medical teams. The CLM leads the country cross-functional Investigator Site Selection Team; prepares Core Country Study Documents to initiate the trial; manages Country Study Budget including estimates and payments; develops the Country Enrollment Plan; tracks country site initiation; enrollment and data cleaning activities to ensure they remain in line with country commitments.
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