Senior Lab Project Services Manager

Study Activity Monitoring and Closeout

• Monitor project plans, timelines, deliverables, and study progress throughout the project lifecycle.
• Manage study documentation, including sample receipt, testing progress, reporting, and related study activities.
• Conduct meetings to support study execution and customer requirements.
• Manage study scope changes and budgets.
• Monitor study quality and service-related issues and implement changes as required.
• Develop and share lessons learned, where applicable.

Customer and Stakeholder Management

• Build and maintain customer relationships and facilitate effective communication throughout the study lifecycle.
• Collaborate with operational teams across the organization to support study delivery.
• Serve as an escalation point for study-level issues and coordinate resolution activities.
• Coordinate customer survey follow-up activities and ongoing health checks.
• Lead activities that enhance Customer Delivery Team results and strengthen customer governance.
• Serve as an escalation point for program-level issues.

Meetings, Initiatives and Training

• Represent the company at governance meetings and other internal and external meetings as required.
• Participate in audits and inspections as needed.
• Participate in process improvement projects and department initiatives.
• Provide mentoring, guidance, and training support based on experience.
• Provide feedback to management regarding team performance against contracts, customer expectations, and project plans.

Process Improvement and Special Assignments

• Act as a task owner or Subject Matter Expert, as required.
• Support department-level assignments and special projects.

Qualifications

• Bachelor's Degree in Life Sciences or a related field, or an equivalent combination of education, training, and experience.
• 5+ years of clinical or research industry experience, including at least 3 years of project management and/or project setup experience.
• Excellent interpersonal and customer management skills.
• Thorough understanding of medical and clinical research terminology.
• Thorough knowledge of project management processes, company laboratory processes, or equivalent working knowledge of 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 experience with comparable laboratory systems.
• Experience leading large, global, and complex Phase I-IV clinical trials preferred.
• Demonstrated ability to work in a fast-paced environment with strong organizational skills and the ability to meet deadlines.
• Strong written and verbal communication skills, including a good command of the English language.
• Ability to establish and maintain effective working relationships with coworkers, managers, and customers.

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.