Clinical Trial Manager, Single-Sponsor

hace 4 semanas


Xico, México Icon A tiempo completo

Job Summary

The Clinical Trial Manager (CTM) is a critical role within ICON, responsible for the delivery of all clinical aspects of a study. This includes overseeing the clinical portion of the budget, developing monitoring plans and tools, training Clinical Research Associates (CRAs), driving enrollment and study start-up activities, reviewing trip reports, implementing corrective and preventative action plans, and liaising with the Sponsor, vendors, and cross-functional teams.

Key Responsibilities

  • Develop and implement clinical strategies to ensure study deliverables are met
  • Oversee the clinical portion of the study budget and ensure timely and within-budget delivery
  • Develop and maintain monitoring plans and tools to ensure high-quality data collection
  • Train and manage CRAs to ensure they have the necessary skills and knowledge to perform their roles effectively
  • Drive enrollment and study start-up activities to ensure timely and efficient study initiation
  • Review trip reports and implement corrective and preventative action plans as needed
  • Liaise with the Sponsor, vendors, and cross-functional teams to ensure seamless communication and collaboration
  • Identify and mitigate risks that may impact clinical delivery
  • Provide regular reporting and metrics on all clinical activities

Requirements

  • 4-year degree or equivalent combination of education and experience
  • Demonstrated ability to drive clinical deliverables of a study
  • Subject matter expertise in the designated therapeutic area
  • Prior monitoring experience is preferred
  • Ability to travel up to 20%
  • Fluent in local language - both written and verbal

Benefits of Working at ICON

ICON is committed to providing a workplace that is inclusive and free of discrimination and harassment. We offer a competitive salary package and a range of health-related benefits to employees and their families.



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