• Responsible for leading the development and execution of investigational and commercial material global supply strategies for early and late-stage development programs intended for regulatory approvals of new products, new indications, or line extensions of currently approved products.
• Participate as a key member of the Pharmaceutical Sciences Project Team (PSPTI and Co-Development Team (CDT) to proactively recognize and address logistical and regulatory issues associated with the requirements of the clinical development program and project team objectives.
• Participate as a core study team member to provide operational knowledge relating to lnvestigational Product (IP) and lead strategy discussions.
• Proactively anticipate changes based on operational factors (countries, sites, enrollment), randomization configuration and protocol requirements.
• In partnership with the CST, develop clinical supply solutions, including packaging, blinding, and distribution strategies, that meet the needs of clinical studies as well as ensure patient compliance and safety.
• Proactively identify risks and develop strategies to mitigate these risks and create contingency plans that minimize the impact of unanticipated events.
• Manage clinical trial drug supply budget and communicate forecasts and changes effectively and in a timely fashion to study teams and GCS partner lines.
• Maintain project information in GCS project tracking systems and in Pharm Sci project management systems.
• Ensure site and patient focus, along with quality compliance, throughout Pharm Sci and GCS processes.
• Act as a point of contact for clinical supply required input during audits and regulatory inspections as well as participate in inspection readiness activities.
• Participate on Limited Duration Teams and Continuous Improvement projects.

• Bachelor's Degree with 7 years of demonstrated and relevant experience in pharma/biotech project management and cross functional team leadership; clinical supply project management experience.
• Demonstrated ability to manage large and complex clinical development programs.
• Demonstrated capability to lead business development activities and acquisitions as they relate to clinical programs.
• Demonstrated knowledge and experience working in a Good Manufacturing Practices (GMP) (c GMP) and Good Clinical Practices (GCP) (Gx P) environment.
• Demonstrated understanding of pharma quality and regulatory framework.
• Demonstrated in-depth experience managing multiple clinical studies in parallel.
• Demonstrated experience leading and delivering in a matrix team environment.
• Working knowledge of MS office applications including MS Project and Office Timeline-Pro.
• Demonstrated excellent computer, 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.
• Demonstrated ability to develop and maintain clinical supply demand forecast and budgets.

• Relevant pharmaceutical experience.
• Relevant operational experience across diverse business portfolio. {e.g. Biopharmaceuticals, Consumer Products, other industries}
• Past oral presentations at conferences and other large audiences.
• Candidate demonstrates a breadth 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 other colleagues to achieve meaningful outcomes and create business impact.

• Last Date to Apply for Job: October 25, 2024
• Eligible for Employee Referral Bonus
• Work Location Assignment: Must be able to work from assigned Pfizer office 2-3 days per week, or as needed by the business.

The annual base salary for this position ranges from $117,300.00 to $195,500.00. In addition, this position is eligible for participation in Pfizer’s Global Performance Plan with a bonus target of 17.5% of the base salary and eligibility to participate in our share based long term incentive program. We offer comprehensive and generous benefits and programs to help our colleagues lead healthy lives and to support each of life’s moments. Benefits offered include a 401(k) plan with Pfizer Matching Contributions and an additional Pfizer Retirement Savings Contribution, paid vacation, holiday and personal days, paid caregiver/parental and medical leave, and health benefits to include medical, prescription drug, dental and vision coverage. Learn more at Pfizer Candidate Site – U.S. Benefits | (uscandidates.mypfizerbenefits.com). Pfizer compensation structures and benefit packages are aligned based on the location of hire. The United States salary range provided does not apply to Tampa, FL or any location outside of the United States. Logistics & Supply Chain Mgmt #LI-PFE