Global Clinical Trial Delivery Lead

IQVIA LLC; Marietta (GA); On-site; USD 90,000 - 130,000; Full time

Job summary

IQVIA Laboratories in Marietta, GA seeks a Project Delivery Program Lead to manage the operational delivery of complex clinical research studies and global customer programs. You will drive study planning, governance, and continuous improvement while ensuring compliance with SOPs and quality practices.

You will develop project plans, milestones, budgets and deliverables; lead customer meetings and escalate program issues; monitor study activities and eTMF filing; and mentor teams to improve

Qualifications

• Bachelor's degree in Life Sciences preferred.
• 5–7 years of experience in clinical trials, project management or a laboratory environment.
• Knowledge of project management processes and central laboratory operations.
• Proficiency with Microsoft Office and centralized laboratory systems preferred.
• Experience leading large, global Phase I–IV trials preferred.

Responsibilities

• Lead the setup and delivery of complex clinical research studies and global customer programs.
• Develop and maintain project plans, milestones, risk/issue/action logs, budgets, timelines and deliverables.
• Partner with Study Setup teams to support database configuration and protocol documentation.
• Build and manage customer relationships; lead meetings and handle escalation for study issues.
• Monitor study activities, eTMF filing, reporting, scope changes and closeout requirements.
• Prepare and present materials at kickoff and investigator meetings; train sites and customers.
• Lead program processes, drive best practices and mentor department staff.

Skills

Interpersonal skills

Customer management

Project management

Communication skills

Cross-functional teamwork

English proficiency

Time management

Education

Bachelor's degree in Life Sciences

Tools

Microsoft Office

Central laboratory systems

Job description

IQVIA Laboratories in Marietta, GA seeks a Project Delivery Program Lead to manage the operational delivery of complex clinical research studies and global customer programs. You will drive study planning, governance, and continuous improvement while ensuring compliance with SOPs and quality practices.

You will develop project plans, milestones, budgets and deliverables; lead customer meetings and escalate program issues; monitor study activities and eTMF filing; and mentor teams to improve