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support study start up activities, as needed.

Key accountabilities: 
• Executes and delivers the GCO supported clinical studies; guides planning and decision making at study level 
• Acts as the CTT product owner with clear and focused duties and responsibilities per the agile ways of working 
• Active member of a Clinical Operations community within PSP supporting the COPH and SL 
• Promotes operational excellence in the development of global clinical study protocol (s), clinical study report (s), and other study-related documents

Deliverables:
• Patient recruitment, clinical data, study documentation and study reports 
• Proactive, iterative operational planning with effective contingencies and embedded risk management mindset in CTT

Key skills: 
• Leadership skills in a matrix environment, with multidisciplinary and networking teams 
• Excellent negotiation and conflict resolution skills and enterprise mindset 
• Clinical Trial Team (CTT) 
• GCO sub team

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com