- 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
- 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
Core Competencies
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 Management
- Clinical Operations
- GxP Regulations
- ICH Regulations
- Contracting
ATS Optimization Keywords
Hard Skills
- Clinical Trial Design
- Vendor-Related Risk Management
- Operational Procedures
- Performance Standards
- Budget Management
Soft Skills
- Collaboration
- Proactive Problem Solving
- Communication
Industry Keywords
- Clinical Trials
- Vendor Start-Up Management
- Supplier Service Specifications
- Study Start-Up Processes
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