Global Trial Delivery Lead

IQVIA Inc; Reading; Hybrid; GBP 85,000 - 120,000; Full time

Job summary

IQVIA is seeking a Global Trial Delivery Manager to lead the Study Management Team and coordinate global clinical trial activities from planning through close-out. You will ensure inspection readiness and drive timely, compliant delivery across regions, liaising with country staff, CROs and vendors.

The role requires strong leadership, advanced therapeutic area knowledge, and experience managing virtual global teams, with a focus on risk mitigation and process improvements.

Qualifications

• BS degree or equivalent in Life Sciences.
• 6-8 years clinical trial management experience in the pharmaceutical industry or CRO.
• Strong working knowledge of ICH-GCP, local laws and regulations.
• Proven leadership to proactively drive the Study Management Team.
• Experience coordinating global or regional teams in a virtual environment (2–3 years).
• Strong project planning/management and budgeting abilities.
• Proficiency with standard Microsoft applications and trial management systems.

Responsibilities

• Lead the Study Management Team and provide updates on deliverable status.
• Ensure availability of reports to support real-time trial status tracking.
• Manage documentation and communications of trial progress.
• Maintain inspection readiness and ensure SOP compliance across regions.
• Coordinate with global trial leads to plan start-up, execution and close-out.
• Monitor budgets and vendor spend; review invoices and variances.
• Contribute to cross-functional documents and data collection for site feasibility.

Skills

Leadership

GCP

Study Management

Budgets

Communication

Education

BS Life Sciences

Tools

Trial Master File

CTMS systems

Job description

IQVIA is seeking a Global Trial Delivery Manager to lead the Study Management Team and coordinate global clinical trial activities from planning through close-out. You will ensure inspection readiness and drive timely, compliant delivery across regions, liaising with country staff, CROs and vendors.

The role requires strong leadership, advanced therapeutic area knowledge, and experience managing virtual global teams, with a focus on risk mitigation and process improvements.