Associate Clinical sourcing Manager
13 hours 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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