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Director, Project Management (Peri-Approval & Observational Research)

US-North Carolina-Raleigh, ICR; US-Pennsylvania-North Wales; Spain-Barcelona
Permanent
Reference: 045789
Description
Are you a seasoned clinical research Portfolio Director with experience leading global programs and teams in Peri-Approval & Observational Research studies?
 
Location: Any US ICON Office or Home-Based
 
Director, Project Management (Peri-Approval & Observational Research) role at ICON:
This Director, PM falls within ICON’s Commercialization & Outcomes division and will be part of our observational research department. Provide leadership to effectively coordinate and manage the activities of a large cross functional multinational portfolio of studies and project teams in a manner that ensures all timeframes and targets are met and that costs are kept under control.
 
Develop late phase project plans for a portfolio of studies including Interventional, EAP, Post Marketing Surveillance, Post-Authorization Safety Studies, Registries, Chart Review, Real World Evidence and Pragmatic Studies. Will subsequently lead cross functional study teams in accordance with contractual timelines, client specifications and Good Clinical Practices (GCPs).
 
Effectively manage study budgets to ensure financial targets are met through regular review of indirect costs and project resources. Provide coaching and mentoring to Project Managers (PMs) and Clinical Trial Managers (CTM’s) and contribute to department training initiatives, as appropriate. Coordinate and manage the activities of individuals, studies and staff in a manner that ensures all timeframes and targets are met and that costs are kept under control.
 
Benefits of Working in ICON:
ICON provides 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. A minimum of ten (10) years of full service project management (US only) or nine (9) years of single service project management. Therapeutic experience in across a wide array of complex late phase services including peri- approval & observational research. Track record of successfully managing large/complex global cross functional projects; strong domestic and international project management experience. 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 - Minorities/Females/Disabled/Veterans and committed to providing a workplace free of any discrimination or harassment.
 
*LI-ZS1
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