Lead and manage matrix teams responsible for the end-to-end oversight of supply chain activities required for the provision of investigational product on phase I-IV protocols for both Small Molecule and Biologics programs.
Provide consultation on all aspects of investigational product strategies and a key decision maker for the development of investigational product supply and sourcing strategies.
Responsible for designing strategies that align with program, protocol, and regulatory requirements, identifying and managing supply chain risk, managing multi-million clinical supply budgets, and providing guidance and leadership to the Clinical Supply Team (CST).
Oversee the end-to-end activities and identify potential risks and develop supply strategies that balance cost, timelines, and risks to support the development of candidates in the Pfizer Research & Development teams across the multiple business units within Pfizer.
Accountable for Pfizer clinical supplies delivery and oversight of end-to-end process from API to finished product delivery to clinical sites.
Key Global Clinical Supply (GCS) point of contact for clinical study teams, Co-Development Teams (CDTs), asset teams, and Clinical Research Organizations (CROs) and represents GCS and MedSci functional lines at the core study team.

BA/BS with 8+ years of demonstrated and relevant experience in pharma/biotech project management and cross functional team leadership.
Demonstrated knowledge and experience working in a Good Manufacturing Practices (GMP) (cGMP) and Good Clinical Practices (GCP) (GxP) environment.
Demonstrated understanding of pharma quality and regulatory framework.
Demonstrated experience leading and delivering in a matrix team environment.
Demonstrated electronic, written and verbal communication skills.
Demonstrated breath of diverse leadership experiences and capabilities, including the ability to influence and collaborate with peers, develop and coach others, oversee and guide the work of colleagues to achieve meaningful outcomes and create business impact.
Demonstrated understanding of late-stage clinical drug development processes.
Demonstrated ability to inspire teams to deliver in a dynamic business environment through effective change management and leadership.

Supply Chain Lead – Secondment 12-18 Months

Key skills