Summary
Core member of the Clinical Trial Team (CTT), independently managing all vendor-related
aspects of global clinical trial(s) to deliver study outcomes within schedule, budget,
quality/compliance and performance standards.
Proactively manages vendor-related risks and potential issues. Implements global
vendor strategy and if required, escalates vendor issue
About The Role
Major accountabilities:
- Close interaction and collaboration with study team lead and study team members during study lifetime.
- Review of vendor related protocol sections during protocol development
- Collaborate with Vendor startup manager to the development of Study Specification Worksheet (SSW) to facilitate bid process. If no VSM is assigned to the category, drive the SSW completion.
- Manages interface with vendors in cooperation with vendor partner functions
- Quote/proposal review in collaboration with procurement, support contract negotiations, Contributes to the development of vendor contract amendments. Accountable for vendor cost control, budget review, invoice reconciliation and PO close-out
- Creates and maintains vendor-related risk maps with contingency plan for documentation.
Key Performance Indicators
- Timely, efficient and quality execution of trials & trial related activities within assigned clinical program(s) within budget, and in compliance with quality standards.
- Adherence to Novartis policy and guidelines and external regulations.
Work Experience
- Clinical Trial Managment
- Clinical Trial Vendor Management
- Critical Negotiations.
- Collaborating across boundaries.
Skills
- Trial vendor management.
- Clinical Trials.
- Negotiation Skills.
- Project Management.
- Project Planning.
- Vendor Management.
Languages
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