As a Clinical Trial Liaison you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.
What you will be doing:
The Clinical Trial Liaison (CTL) will develop relationships with clinical trial investigators and research site staff, playing a critical role in ensuring the successful execution of the trial at the site level. The CTL will work in concert with clinical research associates (CRAs) to ensure that investigators and site staff have a thorough understanding of the protocol and logistics of the study, including and all study procedures, to facilitate a white glove experience for the patient journey. The CTL must also understand how the trial fits into the site’s pattern of treatment for the condition and how any competing clinical trials or upcoming drug approvals may affect the progress of recruitment. Repeated interactions will be needed over the course of the trial to ensure that the trial remains “top of mind” with investigators and staff. The CTL will function as part of the study team and will interact frequently with sponsor companies and their field personnel. Furthermore, the CTL will serve as liaison with key investigators to help ensure that they receive prompt assistance with any queries and that any concerns they have are promptly transmitted to the trial’s sponsor.
Provide detailed reports of interactions with investigators and site staff and support TMF maintenance
You are:
What ICON can offer you:
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