Clinical Trial Liaison

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.

Clinical Trial Liaison - POLAND - Homebased

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 Liaison (CTL), Medical Science Liaison (MSL), study coordinator, research pharmacist or administrator.• Fluency in English.• Ability to travel up to 50%.

Benefits of Working in ICON:Our success depends on the knowledge, capabilities and quality of our people. That’s why we are committed to developing our employees in a continuous learning culture – one where we challenge you with engaging work and where every experience adds to your professional development.At ICON, our focus is to provide you with a comprehensive and competitive total reward package that comprises, not only an excellent level of base pay, but also a wide range of variable pay and recognition programs. In addition, our best in class employee benefits, supportive policies and wellbeing initiatives are tailored to support you and your family at all stages of your career - both now, and into the future.ICON, including subsidiaries, 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.