Clinical Project, Feasibility Analytics Manager

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. The Clinical Project Manager/Feasibility role is responsible for leading feasibility activities in clinical trial planning and delivery, ensuring high-quality outputs that inform study planning and accelerate trial start-up.

Responsibilities:

• Ensure all services adhere to policies, local regulatory requirements, and ICH-GCP guidelines
• Collaborate with Global Program Leads (GPLs), Global Trial Leads (GTLs), and study teams to execute feasibility-related objectives
• Perform feasibility activities including: Program/protocol feasibility, Country and site selection, Data compilation and analytics development, Creation of presentation-ready slides for study teams
• Develop integrated feasibility plans aligned with study objectives and timelines
• Partner with analytics teams, study team members, and country contacts to deliver feasibility outputs on time and with high quality
• Support survey distribution, follow-up, and response analysis
• Assist with site list development, management, and communication
• Generate content for newsletters and other communications to ensure successful execution of feasibility processes
• Act as a Global Feasibility Lead within a therapeutic area, managing a book of work autonomously
• Lead end-to-end feasibility processes for assigned studies
• Ability to establish and implement data analytics methodologies
• Collaborate with cross-functional teams to identify risks and implement mitigation strategies
• Monitor progress against feasibility timelines and proactively communicate updates to stakeholders
• Contribute to lessons learned and best practices for continuous improvement
• Support staff development and mentor less experienced team members on feasibility processes

Requirements:

• Bachelor's degree required
• Minimum 3+ years of pharmaceutical industry experience in roles such as data procurement, business development, data strategy, or similar
• 3+ years as part of a clinical trial feasibility team at a pharma or CRO
• Advanced experience in statistical analysis and analytics models with an emphasis on enrollment, simulation, and forecasting
• Advanced PowerPoint skills and intermediate Excel proficiency
• Strong organizational skills and ability to manage multiple projects
• Understanding of assigned therapeutic area
• Ability to analyze survey results and compile insights
• Excellent written and verbal communication skills, including compelling slide design
• Proven success working within a matrix organization to deliver high-quality outputs
• Extensive experience in feasibility analytics interpretation
• Effective leadership capability and ability to foster team productivity and cohesiveness
• Direct feasibility experience preferred