Are you a seasoned clinical research project management leader with Clinical Supplies experience and knowledge of Importer of Record processes?
Program Manager (PMO – Importer of Record) role at ICON:
As a Program Manager within our PMO team, you will provide leadership to effectively coordinate and manage the activities within the PMO regarding Importer of Record and provide oversight to the Clinical Supplies Management group in a manner that ensures all timeframes and targets are met and that costs are kept under control.
Develop full service project plans for clinical trials or a program of studies and subsequently lead cross-functional study teams in accordance with contractual timelines, client specifications and Good Clinical Practices (GCP’s). Effectively manage study budgets to ensure financial targets are met through regular review of indirect costs and project resources. Provide coaching/mentoring to Project Managers (PM’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 our Program Managers 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 base salary, corporate bonus plan, 5+ weeks paid time away from work, and other incentives along with working from home and an opportunity to grow your career within our PM department
Bachelor’s Degree in science or equivalent degree and a qualification in Project Management or equivalent (PMI certification) is desirable. A minimum of 6 years of full service project management or 8 years of single service project management. Proven track record of successfully managing large & complex, global cross-functional projects with strong domestic and international project management and Clinical Supply experience, as well as knowledge of Importer of Record processes and GMP experiencepreferred. Willingness to travel up to 25% as needed.