Associate Clinical sourcing Manager
1 week ago
Job Description Summary
The Associate Clinical Sourcing Manager supports Novartis clinical trials by managing sourcing activities for Contract Research Organisations (CROs). Ensure compliant, timely, and cost-effective external service delivery to enable the Novartis drug development pipeline.Job Description
Key Responsibilities- Prepare and release RFI, RFP, and RFQs; negotiate with suppliers for new requests and scope changes.
- Act as primary contact for vendors on scope of work, assumptions, pricing, and payment schedules.
- Negotiate, develop, and execute contract frameworks (MSAs, SLAs) with key suppliers and ensure implementation.
- Collaborate with legal, finance, and QA to ensure agreements minimise risk and deliver commercial advantage.
- Drive supplier selection based on category strategy, value-added services, and cost optimisation.
- Monitor compliance, reduce maverick spend, and deliver annual productivity improvements.
- Manage complete contract packages for clinical ESP activities, ensuring SOX and company compliance.
- Support vendor audits and corrective action plans.
- Track supplier performance against expectations and contracts.
- Identify and implement innovative sourcing solutions to create value.
- Plan and manage projects considering priorities, resources, budgets, and constraints.
- Build sustainable stakeholder relationships across business structures and networks.
- Bachelor's degree in Life Sciences, Chemistry, Biochemistry, or Pharmaceutical Sciences.
- Minimum 5 years' experience in Clinical Development, Pharma R&D, or Procurement.
- Minimum 5 years' experience in outsourcing within Pharma or CRO industry.
- Fluent in English and French (spoken and written).
- Master's degree or MBA in business administration or scientific field.
Skills Desired
Internal And External Customer Needs Analysis & Satisfaction Studies, Negotiating, Root Cause Analysis And Problem-Solving, Vendor Management-
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