Clinical Project Manager - Global Study Lead

IQVIA LLC; Reading; On-site; GBP 65,000 - 95,000; Full time

Job summary

IQVIA is seeking a SSO Clinical Project Manager (CPM) to lead day-to-day planning, execution, and reporting of assigned studies from site initiation to close-out in the UK. You will be the single point of contact for country/cluster/hub studies, coordinating with Trial Leads, CRAs, and local QA to ensure compliance and on-time delivery.

The role requires strong leadership, communication, and risk-management skills, with experience in clinical operations and GCP.

Qualifications

• Bachelor's Degree in Life sciences or related field
• Strong written and verbal communication in English
• Proven project management experience in clinical operations

Responsibilities

• Supports study startup and planning activities with timelines
• Identifies risks and mitigations for assigned studies
• Maintains study protocols knowledge to answer operational questions
• Leads study team meetings and coordinates with CRAs and managers
• Monitors study progress, budgets, and data quality
• Ensures site readiness and adherence to GCP and SOPs
• Coordinates training and documentation for monitoring activities

Skills

Project coordination

Communication

Leadership

Problem solving

Organization

Education

Bachelor's Degree Life sciences or related field

Tools

MS Office

Job description

IQVIA is seeking a SSO Clinical Project Manager (CPM) to lead day-to-day planning, execution, and reporting of assigned studies from site initiation to close-out in the UK. You will be the single point of contact for country/cluster/hub studies, coordinating with Trial Leads, CRAs, and local QA to ensure compliance and on-time delivery.

The role requires strong leadership, communication, and risk-management skills, with experience in clinical operations and GCP.