Senior Project Management Analyst

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. The Senior Project Management Analyst will provide operational support and coordination for global clinical trials, ensuring efficient trial execution from planning through close-out.

Responsibilities:

• Plan, coordinate, and execute clinical trial activities across regions in compliance with ICH-GCP, ensuring timely and high-quality delivery
• Maintain and oversee trial documentation (e.g., ISF, TMF, submissions), ensuring completeness, accuracy, timeliness and audit readiness
• Collaborate with global and regional stakeholders, vendors, and trial teams to ensure seamless trial conduct and communication
• Manage and maintain clinical trial systems, databases, and tracking tools ensuring data accuracy
• Prepare and distribute project plans, status updates, reports, and presentation materials
• Monitor trial progress, budgets, and system data, identifying risks and implementing corrective actions as needed
• Coordinate documentation workflows, regulatory submissions, and communication with authorities and regional teams
• Support reporting, trial close-out activities, and preparation of key deliverables (e.g., CTR appendices)
• Coordinate logistics for trial meetings, materials, and supplies
• Contribute to quality oversight, inspection readiness, and best practices in clinical trial conduct
• Act as a key point of contact for trial-related systems, documentation, and operational queries

Requirements:

• University degree qualified and/or comparable professional education with at least 3+ years' experience in clinical trial operations or project coordination
• Exceptional communication and stakeholder management skills
• Strong knowledge of applicable clinical research regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
• Excellent organizational and problem-solving skills with ability to work independently, prioritize tasks, and manage projects in a complex international environment
• Detail-oriented with strong commitment to quality and compliance
• Proficiency in MS Office and clinical trial systems/tools
• Fluent in written and spoken English