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Novartis

Senior Trial Vendor Manager

Novartis

Trial Vendor Senior Manager at Novartis managing vendor relationships and ensuring compliance in clinical trials. Collaborating with teams to achieve timely and high-quality study outcomes.

Posted 7/21/2026full-timeLondon • 🇬🇧 United KingdomSenior💰 £49,140 - £91,260 per yearWebsite

Core Competencies

Role fit
Core Competencies

Use this summary to align your resume positioning with the role.

Demonstrates expertise in managing vendor-related operational deliverables for global clinical trials, ensuring compliance with GxP and ICH regulations while optimizing study start-up processes. Proficient in vendor management, contracting, and collaboration with clinical trial sites.

Highest-signal resume keywords
Vendor ManagementClinical OperationsGxP RegulationsICH RegulationsContracting

ATS Keywords

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Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills
Clinical Trial DesignVendor-Related Risk ManagementOperational ProceduresPerformance StandardsBudget Management
Soft Skills
CollaborationProactive Problem SolvingCommunication
Industry Keywords
Clinical TrialsVendor Start-Up ManagementSupplier Service SpecificationsStudy Start-Up Processes

About the role

Key responsibilities & impact
  • Accountable for all vendor related operational trial deliverables, according to timelines, budget, operational procedures, quality/compliance and performance standards
  • Collaborate with the Vendor Start-up Manager for the VSM’s specific responsibilities
  • Manage all vendor-related aspects of global clinical trial(s) to deliver study outcomes within schedule, budget, quality/compliance and performance standards
  • Proactively manage vendor-related risks and potential issues and implement global vendor strategy
  • Optimize study start-up processes and manage central vendor-related activities

Requirements

What you’ll need
  • Bachelor’s degree or equivalent; advanced degree preferred
  • Fluent in English (oral and written)
  • Minimum of 3 years’ experience in clinical operations and vendor management processes
  • Strong knowledge of GxP and ICH regulations, clinical trial design, and supplier service specifications
  • Proficiency in vendor management, contracting, and site-related collaborations

Benefits

Comp & perks
  • Commitment to Diversity and Inclusion
  • Opportunities for professional development
  • Work-life balance support
  • Generous paid time off policies
  • Inclusion in an outstanding, inclusive work environment