Provide comprehensive outsourcing support including but not limited to:  RFP review, CRO Q&A consolidation, proposal distribution and analysis, CRO bid defense meeting coordination and follow up, proposal scorecard development and score compilation, drive internal decision making timelines and vendor selection, and lead all contract and budget negotiations through execution.

A pharmaceutical outsourcing professional with 20+ years of cross-functional experience in the Pharmaceuticals and Medical Device industries.  I have a proven track record of developing and implementing successful sourcing strategies across various R&D and Consulting supply categories in major corporations and Biotechs; have streamlined processes to enhance contracting efficiencies and improve quality of sourced services via program level sourcing; developed strategic client-vendor (CRO, Central Labs, Imaging and Core Labs) relationships and Supplier Relationship…

The role of Clinical Supply Chain Consultant will provide leadership in all aspects of clinical trial

supply management and execution for Alladapt’s Phase I/II study. The focus of this role will be to help coordinate

clinical labeling and packaging, participate in IXRS vendor selection if necessary, IXRS set up and management for

supply, and all inventory and order operations for…

• Currently work on integration of Clinical Trial Operations, Protocol Builder, Patient Recruitment, Informed Consent, Trials Monitoring = Decentralization of Trials with Identity Management and Decentral Ledger Techhnologies, IoT Architecture 

I work for Linux Foundation Hyperledger Patient Data and IEEE Committee for IoT Interoperability for Medical Devices, PhUse FHIR Implementation Framework for Clinical Trials Operations 

• Dynamic and highly motivated, results-oriented global leader, with over 20 years’ experience in Senior Program and Project management roles across industries, managed Strategy Alignment…

CPO duties