Associate Director leading clinical procurement and contracting operations for global clinical trials at Biogen. Focusing on operational excellence, compliance, and financial discipline.
Responsibilities
Lead end-to-end Demand planning and Clinical Contract Delivery operations supporting global clinical trials (Phase I–IV), ensuring timely, compliant execution of sourcing and contracting activities.
Design and optimize a scalable CPSC operating model aligned to portfolio growth.
Establish a technology-enabled Demand planning and Clinical contract delivery environment.
Implement predictive contracting capabilities using historical study data and demand trends.
Define and monitor KPIs (cycle time, quality, compliance, stakeholder satisfaction) and deliver performance transparency to senior leadership.
Lead continuous improvement initiatives across SOPs, templates, legal support models, training, and systems.
Establish and oversee an integrated Vendor Demand Management Model ensuring consistent program-level outsourcing strategies are implemented effectively at study level.
Translate program and portfolio forecasts into structured resource capacity planning and prioritization frameworks.
Ensure clear handoffs of study specifications and contracting requirements into CPSC execution teams.
Serve as escalation point for contracting risks, timeline conflicts, and cross-functional barriers impacting study start-ups.
Drive financial transparency and discipline across contracting activities, including Fair Market Value (FMV) governance, milestone-payment alignment, and value reporting.
Develop and report Commercial Framework Contractual Compliance Metrics, tracking adherence to approved rate cards, templates, commercial protections, and negotiated terms.
Ensure audit readiness, regulatory compliance, and strong documentation practices.
Monitor contractual control effectiveness, identifying systemic gaps and leading corrective process enhancements.
Implement an integrated supplier risk and performance management framework.
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