Senior Director Clinical Site Operations Lead

hace 1 mes


Madrid, Madrid, España Pfizer A tiempo completo
Job Summary

Pfizer is seeking a Senior Director Clinical Site Operations to join our team. As a key member of our operations team, you will be responsible for delivering strategic vision and representing Pfizer operations at the country or cluster level.

Key Responsibilities
  • Represent Pfizer at the country or cluster level, establishing and cultivating relationships with key opinion leaders, strategic sites/networks, health authorities/governments, and industry clinical research associations.
  • Support and cultivate a collaborative partnership with Medical Affairs, creating a framework for an end-to-end continuum linking investigator relationships to future prescribers within the country.
  • Influence leadership decisions that impact business, building and leveraging constructive internal relationships within Pfizer and PRD to drive strategic initiatives/success.
  • Demonstrate knowledge and understanding of the local marketplace and industry trends, providing insights and enabling teams to successfully position and deliver oncology clinical trials.
  • Lead the GSSO organization within their country/cluster to deliver the Pfizer oncology portfolio, driving a meaningful increase in patient recruitment while meeting and exceeding speed and quality deliverables and best-in-class cycle times to bring medicines to patients faster.
Requirements
  • Ensure appropriate Site Care Partner and Site Monitor resources are in place to deliver on country and site-level end-to-end activities in line with study milestones in the designated countries/clusters.
  • Provide line management and oversee the Site Care Partner and Site Monitor ensuring compliance with training requirements.
  • Accountable for overall monitoring, operational site partnership, management, and oversight activities within a designated country/cluster and supervise the monitoring and oversight activities of sites to ensure patient safety and quality of study execution in accordance with applicable laws, Good Clinical Practice, and Pfizer standards.
  • Overall accountability for the growth and development of the Site Operations organization (Managers and Individual Contributors) and to ensure compliance with training requirements.


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