Global Clinical Project Manager - Vendor Management Expert – Single Sponsor (Novartis)

Skills, Experience, Qualifications, If you have the right match for this opportunity, then make sure to apply today.Are you an experienced Vendor Management professional looking to make an impact in global clinical trials?We are seeking a

Global Clinical Project Manager - Vendor Management Expert

to join our

Single Sponsor Department , dedicated exclusively to

Novartis . In this role, you ''ll become an expert in

Vendor Management

for global clinical trials across all phases (Phase I–IV), ensuring seamless execution from study start-up through close-out.What We’re Looking ForTo excel in this role, you should bring:Global Clinical Project Management experienceStrong Vendor Management expertise:

Central lab, eCOA, IRT, ECG, Imaging, Ancillaries and/or Patient Recruitment and Retention with experience in global clinical trials. (must have experience managing at least 2 of these vendors)Deep understanding of clinical operations processes

and vendor service categories.Excellent project management skills

to drive efficiency and collaborationStrong communication and influencing abilities

to partner effectively across functions.Proven ability to manage risk and performance issues

in a fast-paced environmentWhat You’ll DoAs a

Global Clinical Project Manager - Vendor Management Expert , you will be responsible for ensuring vendor deliverables are met with

quality and efficiency

at the trial level. Your key responsibilities include:Vendor Oversight and Coordination

– Manage vendor activities across the study lifecycle, ensuring timely and high-quality deliverables.Study Start-Up Support

– Oversee vendor deliverables during study initiation, ensuring smooth onboarding and activation.Risk and Performance Management

– Track vendor performance, identify risks, and escalate issues as needed.Site Readiness and Activation

– Drive vendor activities to support site activations and ensure study milestones are met.Study Close-Out

– Coordinate vendor deliverables that support Database Lock and study closure.What You’ll DeliverVendor service excellence at the study levelVendor onboarding and performance trackingKPI (Key Performance Indicator) and KQI (Key Quality Indicator) dashboards to monitor vendor effectivenessSite readiness monitoring and documentationRisk mapping with contingency planningVendor cost control and oversightPlease note this role is not eligible for the UK visa sponsorship.This is an exciting opportunity to play a

critical role in global clinical trials , ensuring vendor excellence and operational success. If you’re ready to take on a

high-impact role

with a leading sponsor, we’d love to hear from you!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