Home-Based in Ireland, Poland, Spain, United Kingdom, Romania, South Africa

Latvia, Lithuania, Czechia, Hungary, Serbia, Bulgaria, Portugal, Slovakia, Estonia, Slovenia, Finland, Sweden, Norway, Denmark, Israel, Greece and Italy.

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.

Sr Project Manager - RWE Late Phase studies (EU wide)

Are you a Sr Project Manager with experience in late phase studies, passionate about playing a key role within driving the overall management for regional and global clinical research projects?

ICON's Global RWE (real world evidence) late phase project management team is looking for an experienced Project Manager to join their EU based team.

Role overview:

As a Sr Project Manager you will be expected to contribute towards a culture of business excellence with a focus on quality, scope, timelines adding value to the business and exceeding client expectations. You would be involved at the forefront of innovation and drive delivery using your project leadership expertise. Delivering successful working relationships with clients, cross functional project planning, scheduling and implementation, defining project scope, resource requirements and deliverables, risk mitigation strategies, associated action plan and issue resolution and budget management.

• Delivering successful working relationships with clients, cross functional project planning, scheduling and implementation, defining project scope, resource requirements and deliverables, risk mitigation strategies, associated action plan and issue resolution and budget management

• Work in matrix teams on global international projects and be responsible for the overall coordination, implementation and completion of regional/global cross functional projects

• Provide expert project management input into new business proposals and bid defense meetings

Role requirements:

• Bachelor's Degree in medicine, science or equivalent degree are desirable

• Demonstrable Sr Project Management experience within clinical research is essential

• Demonstrable experiencewithinlate phase studies in a CRO environment, needed

• Strong communication, planning, decision-making, negotiation, conflict management and time management skills

• Experience in global/ multi country studies

• Willingness to travel up as needed

Benefits of working in 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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