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Senior Project Manager, ICO (Peri-Approval & Observational Research)

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About the role

This vacancy has now expired. Please click here to view live vacancies.
Are you an experienced Project Manager with experience in late phase studies? Are you passionate about playing a key role in the overall leadership of large, complex clinical research projects?
 
Apply now to learn why ICON was rated by Forbes as a 2017 Top Employer in America! 
 
Senior Project Management role within ICON Commercialization & Outcomes at ICON:
As a Senior Project Manager within our Peri-Approval & Observational Research team, you will have an opportunity to contribute towards a culture of business excellence with a focus on streamlining processes, adding value to the business and exceeding client needs. You will be the primary point of contact for designated projects, responsible for: delivering successful working relationships with clients, cross functional project planning, scheduling and implementation, defining project scope, resource requirements and deliverables, risk migration strategies, associated action plan and issue resolution. 
 
Manage a cross functional project team ensuring all necessary project training is provided and developing a succession plan for the core team members.  Manage projects in accordance with the contract including: study budget, study invoicing procedures, monitoring and reporting on progress of projects to stakeholders and implementing QC activities as necessary. Collaborate with business development to ensure proactive commercial aptitude while partnering with internal and external stakeholders to identify new avenues for growth.
 
Benefits of Working in ICON:
We provide Project Manager’s with the innovative resources to be successful in delivering results, inspiring others and becoming a trusted partner. We offer an exceptional benefits package that includes a comprehensive health plan, retirement plans, highly competitive pay, corporate bonus plan, time away from work, and many other incentives amongst an opportunity to grow your career within our PMO.
 
Role Requirements:
Bachelor’s Degree in medicine, science or equivalent degree and a qualification in Project Management or equivalent (PMI certification) is desirable. At least 5 years experience within clinical research operations is required with about 3 years hands on project management experience is preferred. Comprehensive knowledge of ICH-GCP and late phase research services is essential along with excellent communication, planning, decision-making, negotiation, conflict management and time management skills. Willingness to travel up to 25% as needed.
 
What’s Next?
Following your application you will be contacted by one of our dedicated recruiters and if successful we will be able to provide you with more details about this opportunity.
 
ICON is an equal opportunity employer -  M/F/D/V and committed to providing a workplace free of any discrimination or harassment.
 
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