• Act as secondary Point of Contact for site personnel engaged in IP handling activities as an investigator site.
  • Review reports and provides site specific trackers/dashboards oversight to support IP handling activities.
  • Assist the coordination of IP for predictive patient enrollment to ensure adequate supplies are available.
  • Send shipment notifications and other IP handling reminders to investigator sites.
  • Work closely with the CRP Lead for the assigned protocol(s) and consult with other GCS colleagues to support the clinical supply chain, including IP shipments, temperature excursions, IRT activities, inventory management, IP preparation, administration, and reconciliation.
• Assist in development and provision of IP handling materials.
• Support the evaluation of existing program level. dosing tools for expanded access and grant programs
• Support the CRP leadership on GCS strategic and process improvement initiatives.
• Maintain good working relationships with internal and external partners at Pfizer (e.g., Formulation Scientists, Label Specialists).

• A degree in Pharmacy with at least 2 years of pharmacy practice or equivalent pharmaceutical/biotech industry experience.
• Fluent in written and spoken English.
• Excellent organization, communication, and interpersonal skills.
• Ability to complete multiple projects and meet targeted deliverables and deadlines.

• Hospital pharmacy experience
• Clinical research experience (i.e. CRA/Monitoring)
• Project management experience
• Strong aptitude for learning and utilizing technology and software applications.
• Portuguese or any other foreign language is a plus.
• Knowledge on global regulatory policies.

Work Location Assignment: Hybrid Research and Development #LI-PFE