Location: Sydney or Melbourne, home-based.
At ICON, it’s our people that set us apart. Our diverse teams enable us to become a better partner to our customers and help us to fulfil our mission to advance and improve patients’ lives.
Our ‘Own It’ culture is driven by four key values that bring us together as individuals and set us apart as an organisation: Accountability & Delivery, Collaboration, Partnership and Integrity. We want to be the Clinical Research Organisation that delivers excellence to our clients and to patients at every touch-point. In short, to be the partner of choice in drug development.
That’s our vision. We’re driven by it. And we need talented people who share it.
If you’re as driven as we are, join us. You’ll be working in a dynamic and supportive environment, with some of the brightest and the friendliest people in the sector, and you’ll be helping shape an industry.
The Role:
The Clinical Trial Liaison (CTL) will foster relationships with clinical trial investigators and other professionals at the site level to optimize patient recruitment for clinical trials for which ICON serves as the CRO. The CTL will work in concert with ICON's CRAs to ensure that investigators and site staff have a thorough understanding of the investigational agents being used in the study, the trial’s eligibility criteria, and all study procedures.
The CTL will function as part of the study team and will interact frequently with sponsor companies and their field personnel.
Further responsibilities:
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.
Deliver relevant scientific and protocol training to site.
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.
Serve as a therapeutic expert for internal ICON staff.
What You Will Need:
• PhD in biological science or related field, PharmD or MD (essential).
• Exposure to the clinical research industry as a Clinical Trial Liasion (CTL), Medical Science Liaison (MSL), study coordinator, research pharmacist or administrator.
• Fluency in English.
• Ability to travel up to 50%.
Benefits of Working at ICON
Our success depends on the quality of our people. That’s why we’ve made it a priority to build a culture that rewards high performance and nurtures talent.
We offer very competitive salary packages. And to keep them competitive, we regularly benchmark them against our competitors. Our annual bonuses reflect delivery of performance goals – both ours and yours.
We also provide a range of health-related benefits to employees and their families and offer competitive retirement plans – and related benefits such as life assurance – so you can save and plan with confidence for the years ahead.
But beyond the competitive salaries and comprehensive benefits, you’ll benefit from an environment where you are encouraged to fulfil your sense of purpose and drive lasting change.
ICON is an equal opportunity and inclusive employer and 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.
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