Senior Project Manager

hace 2 meses


España ICON A tiempo completo

Senior Project Manager, Internal Medicine ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development. At ICON, it’s our people that set us apart. Our diverse teams enable us to become a better partner to our customers and help us to fulfil our mission to advance and improve patients’ lives.Our ‘Own It’ culture is driven by four key values that bring us together as individuals and set us apart as an organisation: Accountability & Delivery, Collaboration, Partnership and Integrity. We want to be the Clinical Research Organisation that delivers excellence to our clients and to patients at every touch-point. In short, to be the partner of choice in drug development.That’s our vision. We’re driven by it. And we need talented people who share it.If you’re as driven as we are, join us. You’ll be working in a dynamic and supportive environment, with some of the brightest and the friendliest people in the sector, and you’ll be helping shape an industry.We are currently seeking a Project Manager to join our diverse and dynamic Internal Medicine team. As a Project Manager, you will be responsible for the overall direction, coordination, implementation, execution, control and completion of global cross-functional or single service projects ensuring consistency with ICON SOPs, study contracts and budgets.What You Will Be Doing:Recognize, exemplify and adhere to ICON's values, which center on our commitment to People, Clients and PerformanceAs a member of staff, the employee is expected to embrace and contribute to our culture of process improvement with a focus on streamlining our processes adding value to our business and meeting client needsTravel (approximately 20-30%) domestic and/or international. Travel to other sites within the network may be required to support increases in workload and/or studies/projects as neededLead the planning and implementation of cross-functional project(s)Facilitate the definition of project scope, goals and deliverablesDefine project tasks and resource requirementsDevelop full-scale cross-functional project plansAssemble and coordinate project staffManage project budgetPlan and schedule project timelinesDevelop and manage risk mitigation strategies for projectsTrack project deliverables using appropriate toolsProvide direction and support to project teamQuality assuranceConstantly monitor and report on progress of the project to all stakeholdersPresent reports defining project progress, problems and solutionsImplement and manage project changes and interventions to achieve project outputsProject evaluations and assessment of resultsOther duties as assignedYour Profile:Bachelor's Degree or 4 year degree equivalentA minimum of 2 years of active Global Full Service Project Management experience with at least 5 years of experience within the pharmaceutical/Clinical industry with experience of managing studies in internal medicine.Thorough knowledge of ICH GCP and relevant regulations for the conduct of clinical trialsBenefits 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.
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