Site Activation Lead

4 semanas atrás


São Paulo, São Paulo, Brasil IQVIA Argentina Tempo inteiro

Job Overview

As a seasoned professional, you will oversee the delivery of site activation, maintenance, and regulatory activities for selected studies or multi-protocol programs. This includes pre-award activities, oversight of the scope of work, budget, and resources. You will lead strategic initiatives and work with senior management to develop implementation plans.

Key Responsibilities

  • Oversee the execution of feasibility, site ID, site activation, and maintenance for assigned projects.
  • Develop and implement management plans according to the scope of work and project plan.
  • Ensure collaboration across feasibility, site ID, regulatory, and site activation teams.
  • Provide specialist functional and technical scientific support to facilitate business development and study initiation.
  • Provide overall guidance and oversight of multi-regional and multi-protocol programs.

Requirements

  • Bachelor's degree in a life science-related discipline.
  • 7 years' relevant experience in a scientific or clinical environment.
  • Experience with site relationship, site identification, and clinical protocol.
  • Thorough understanding of regulated clinical trial environment and knowledge of drug development process.

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