We are seeking an Associate Project Delivery Manager to join IQVIA Laboratories at Marietta, GA.

Job Summary:

What You'll Be Doing:

• Lead study setup activities, including protocol and budget reviews, kickoff meetings, project plans, milestones, and risk, issue, and action logs
• Partner with study setup teams to ensure high-quality database configuration and preparation of protocol-specific documentation and meeting materials
• Monitor project management plans, timelines, deliverables, study documentation, eTMF filing, study reporting, and closeout activities
• Manage study scope changes, budgets, service-related issues, and quality concerns, implementing corrective actions and sharing lessons learned
• Build and maintain strong customer relationships while coordinating communication across operational teams, sites, CRAs, and other stakeholders
• Serve as an escalation point for study-level issues and coordinate the triage and resolution of study-specific risks and challenges
• Represent IQVIA Laboratories at investigator meetings, customer meetings, audits, inspections, bid defense meetings, and other internal or external forums
• Deliver study-specific training to sites, CRAs, customers, and less experienced team members, and contribute to continuous improvement initiatives
   

What We Are Looking For:

• Bachelor's Degree Life Sciences and/or related field
• 2+ years of clinical or research industry experience, including 1 year project management / project set up experience
• Working knowledge of project management processes and central laboratory operations, including kits and supplies, logistics, laboratory operations, specimen storage, data reporting and transfers, and site alerts
• Demonstrated computer proficiency with Microsoft Office and company systems, or equivalent experience with similar centralized laboratory systems
• Other equivalent combination of education, training, and experience may be accepted in lieu of degree
   

The Knowledge, Skills and Abilities Needed for This Role:

• Strong interpersonal and customer management skills, with the ability to establish effective working relationships with coworkers, managers, sites, and customers
• Working understanding of medical and clinical research terminology, with experience supporting Phase I–IV clinical trials preferred
• Strong organizational and time-management skills, with the ability to meet deadlines in a fast-paced environment
• Strong written and verbal communication skills, including a good command of the English language
• Ability to lead cross-functional communication, manage escalations, and coordinate the resolution of project-level issues
   

What We Offer You: