Local Trial Manager

It is a very exciting time at ICON – we’re a world-leading healthcare intelligence and clinical research organisation. 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.

FY 2024 is starting very positively – a number of new projects in our client’s portfolio means that we are augmenting our Clinical Project Management team in Ireland. If you have experience with clinical project management in Ireland we would love to hear from you.

This is a home-based position for staff based (and the requisite right-to-work) in Ireland.

If you are seeking a career where you can truly make a difference in the lives of others, working closely together with the top minds in the pharmaceutical Industry, then here is your chance to join our team of clinical trial managers.

As a sponsor-dedicated clinical trial manager, you will work on an exciting range of clinical trials. You will demonstrate a solid clinical study management track record across Ireland. You can work fully homebased in Ireland

Your will be the primary point of contact to lead, manage and co-ordinate the conduct of clinical trials from study start-up to close out at a country level

You will partner with global, local country teams and study team to provide high level country strategy, drive study progress and country level study delivery.

What is required

• BA/BS/BSc or RN
• Previous experience of project managing clinical studies within the clinical research industry, i.e. within pharma, CRO or biotech working environments.
• Previous clinical study management/project management as a Clinical Study Manager gained in Ireland
• Experience in overseeing external clinical research vendors (CROs, central labs, imaging vendors, etc.) highly preferred
• Ability to use scientific and clinical knowledge to conceptualize study designs
• Full and valid working eligibility

You will be rewarded with a permanent and full-time contract of employment seconded to the client. We will offer you a competitive salary with excellent company benefits

#PMjob

Local knowledge / expertise of regulatory environment, study start up process and associated timelines

Educated to degree level or equivalent. 

Must be based in Ireland and have experience working within that country, preferably with strong management experience.