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The Project Leaderrole requires you to manage cross functional teams and liaise directly between IQVIA functions and the customer, acting as that accountable point for delivery and quality whilst maintaining financial control. You will be supported by domain experts in every function, enabled by best in class technology and data analytics. 

Key collaborators are the Clinical Lead for site management, the Project Vendor Manager, the Project Management Analyst for project coordination, tracking and financial analysis, and the Site Activation Manager as an expert in start-up. 

This is an important and high-profile role within our Research & Development Operation and IQVIA’s size and global footprint will present you with the breadth of opportunities necessary to develop your career.

Typically assigned to one or two projects, or a program, responsibilities might include:

• Leading global cross-functional project team delivery, accountable for achievement of milestones and quality of contracted scope

• Serving as the primary contact with the customer for progress and governance

• Developing study management plans and ensuring consistent use of study tools, training materials and compliance with standard processes, policies and procedures

• Anticipating risk and implementing mitigation strategies

• Managing study team assignments, accountability and resource requirements 

• Ensuring the study budget is managed proactively including scope changes and financial systems are accurate

REQUIRED KNOWLEDGE, SKILLS AND ABILITIES

• Bachelor's degree in life sciences or related field and 5-7 years’ clinical research experience 

• Global project management experience within the drug development industry, with previous CRO experience is ideal. Minimum 4 years prior project management experienceand experience in clinical operations; or equivalent combination of education, training and experience

• In depth therapeutic knowledge in Immunology, CVRM, or Oncology.