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Senior Trial Vendor Manager
NovartisTrial 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.
Core Competencies
Role fitCore 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
Tailor your resumeApplicant 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