Clinical Trial Liaison

As a Clinical Trial Liaison you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.

For our sponsor, a pharmaceutical company specializing in oncology, we are seeking experienced candidates who are eager to help shape the future alongside us! This presents a unique opportunity for Clinical Research Associates ready to advance their careers, as well as for those with relevant experience, as you will be part of an exciting and innovative program!

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.

• Understand the scientific basis of assigned clinical trials
• Serve as main point of contract for the sites (across different studies)
• Support site assessment and selection
• Oncology experience preferred, especially CAR-T
• Create educational materials to effectively communicate the science behind the clinical trial
• Be able to communicate the scientific basis of the trials to other team members, investigators and site staff
• Identify effective prescreening strategies for each trial and recommend improvements
• Provide detailed reports of interactions with investigators and site staff and support TMF maintenance

Your skillset includes:

• Exposure to the clinical research environment as a Clinical Trial Liaison / Site Engagement Liaison, Medical Science Liaison, study coordinator, Senior CRA or experience in a CRO
• Read, write and speak fluent English; Dutch, Frenc
• BA/BS required
• Candidates must be willing to travel up to 50%.

What ICON can offer you:

Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent.

In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.

Our benefits examples include:

• Various annual leave entitlements
• A range of health insurance offerings to suit you and your family’s needs
• Competitive retirement planning offerings to maximise savings and plan with confidence for the years ahead
• Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family’s well-being
• Life assurance
• Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others

Visit our careers website to read more about the benefits of working at ICON: https://careers.iconplc.com/benefits

At ICON, diversity, inclusion & belonging are fundamental to our culture and values. Our rich diversity makes us more innovative which helps us better serve our people, patients, customers, and our communities. We're proud of our diverse workforce and the work we’ve done to become a more inclusive organisation. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know through the form below.

https://careers.iconplc.com/reasonable-accommodations

Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles.

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