09 ott - Monza
Iqvia
OverviewIn this role you will lead delivery of clinical studies, ensuring fast, quality and compliant execution within contracted scope.
You work within the core project team to optimize speed, cost, and outcomes, collaborating with cross-functional groups to overcome obstacles.
You will manage relationships with customers and vendors, forecast opportunities, and drive continuous improvement through lessons learned.
This position offers leadership across studies and a chance to shape operational excellence using IQVIA solutions.
ResponsabilitàDevelop integrated study management plans with the core project team
Execute clinical studies per contract while optimizing speed, quality and cost
Set objectives for the core project team and assess performance
Collaborate with other functional groups to support milestones and manage study issues
Monitor progress and proactively present project status to stakeholders
Identify and manage risks and contingencies, leading problem solving
Ensure project quality by addressing risks and implementing CAPA
May act as primary or backup customer contact and manage key customer relationships
Build and lead cross-functional project teams for on-time delivery and issue resolution
Ensure financial success of the project, forecast opportunities to accelerate revenue
Identify scope changes and manage change control processes
Capture lessons learned and implement best practices
May lead vendor management activities as primary contact
Support staff development and mentor junior team members
Adopt corporate initiatives and communicate change to the team
Provide input on team members' performance relative to project tasks
Collaborate across geographies with awareness of cultural differences
Maintain awareness of project financials and contractual obligations
Demonstrate IQVIA Core Competencies across client focus, collaboration, communication, innovation, and ownership
Requisiti fondamentaliBachelor's Degree Life sciences or related field
3 years of relevant experience including >1 year of project management experience or equivalent
Advanced knowledge of the job area and broad knowledge of related areas
Knowledge of clinical trials and regulatory requirements (ICH GCP, local laws)
Strong written and verbal communication skills in English, with solid presentation abilities
Problem solving skills and results-oriented mindset
Leadership capability to guide cross-functional teams and manage performance
Excellent organization, prioritization, and time management
Quality focus with attention to detail and continuous learning
Proficiency with MS Office (Word, Excel, PowerPoint)
Ability to collaborate with customers and cross-functional teams across geographies
Understanding of project financials and contractual obligations
IQVIA core competencies: Client Focus, Collaboration, Communication, Innovation, Ownership
communication
problem solving
leadership
MS Office (Word, Excel, PowerPoint)
clinical trial conduct knowledge
ICH GCP and regulatory compliance
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