Senior Project Manager

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

Fantastic opportunity for a Senior Global Clinical Trial Manager/ Clinical Project Manager, permanent and fully home-based sponsor dedicated to a top global Pharma on FSP.

Countries we can ONLY consider: Italy, Spain, Turkey, Czech, Poland, Bulgaria and Hungary.

**Please note your application will be rejected if you are not already located in these countries.**

What you will be doing:

• The Senior Clinical Project Manager is responsible for study and regional/country level activities from study startup through conduct and study close. The Senior PM will be assigned one or more studies and will be tasked with taking on several responsibilities in support of the larger Study Management deliverables.
• The Senior PM partners with the Global Study Manager, Study Start Up Project Manager, Site Intelligence Lead, Country Trial Manager, Site Excellence Partners, Site Relationship Partners, Site Care Partners, Contracts Lead, Regulatory Affairs, pCRO and others as required to ensure a coordinated approach to study start up, execution and close out.
• The Senior PM has exceptional knowledge in managing and coordinating specific tasks and responsibilities as part of the larger Study Management team.
• The Senior PM provides leadership and strategic planning and organization skills to ensure the operational delivery of tasks within one or more studies, in accordance with the appropriate quality standards including ICH/GCP standards, SOPs, local operating guidelines and local regulatory requirements, as applicable.

You are:

• Extensive operational clinical trial experience
• A scientific or technical degree is required along with extensive knowledge of clinical trial methodology - BS/BSc/MS/MSc
• BA/BS 7+ years of relevant experience as a Global Clinical Trial Management or Clinical Project Management experience within a CRO or Pharma
• MBA/MS/ 6+ years of relevant experience as a Global Clinical Trial Management or Clinical Project Management experience within a CRO or Pharma
• Expertise in the use of study/site dashboard and reporting tools
• Detail oriented & possesses technical expertise
• Ability to manage complex processes
• Ability to manage in a matrix environment
• Risk Identification & Mitigation
• Strategic Planning, Analytical and Problem-Solving Skills
• Critical Path Analysis
• Excellent communication skills, both written and verbal

Why 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.

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.

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, colour, 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.

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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