Global Clinical Project Manager - Vendor Management Expert - Novartis Dedicated (home-based in Europ
IQVIA - Reading, England
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Global Clinical Project Manager - Vendor Management Expert – Single Sponsor (Novartis)Are you an experienced Vendor Management professional looking to make an impact in global clinical trials? We are seeking aGlobal Clinical Project Manager - Vendor Management Expertto join ourSingle Sponsor Department , dedicated exclusively toNovartis . In this role, you 'll become an expert inVendor Managementfor global clinical trials across all phases (Phase I–IV), ensuring seamless execution from study start-up through close-out.What We’re Looking For To excel in this role, you should bring: Global Clinical Project Management experience Strong Vendor Management expertise:Central lab, eCOA, IRT, ECG, Imaging, Ancillaries and/or Patient Recruitment & Retention with experience in global clinical trials. (must have experience managing at least 2 of these vendors) Deep understanding of clinical operations processesand vendor service categories. Excellent project management skillsto drive efficiency and collaboration Strong communication and influencing abilitiesto partner effectively across functions. Proven ability to manage risk and performance issuesin a fast-paced environmentWhat You’ll Do As aGlobal Clinical Project Manager - Vendor Management Expert , you will be responsible for ensuring vendor deliverables are met withquality and efficiencyat the trial level. Your key responsibilities include: Vendor Oversight & 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 & Performance Management– Track vendor performance, identify risks, and escalate issues as needed. Site Readiness & 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 Deliver Vendor service excellence at the study level Vendor onboarding and performance tracking KPI (Key Performance Indicator) and KQI (Key Quality Indicator) dashboards to monitor vendor effectiveness Site readiness monitoring and documentation Risk mapping with contingency planning Vendor cost control and oversightPlease note this role is not eligible for the UK visa sponsorship.This is an exciting opportunity to play acritical role in global clinical trials , ensuring vendor excellence and operational success. If you’re ready to take on ahigh-impact rolewith 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 athttps:
Created: 2025-09-10