Centralized Monitoring Lead

hace 4 semanas


Xico, México Iqvia A tiempo completo
Job Overview

As a Centralized Monitoring Lead at IQVIA, you will play a key role in leading our clinical trials monitoring team to achieve project objectives and deliver high-quality results to our clients. This position requires strong leadership and collaboration skills, as well as expertise in clinical trial conduct and regulatory requirements.

Key Responsibilities
  • Project Oversight: Oversee clinical deliverables on assigned projects, manage project resources, and coordinate efforts of cross-functional project teams.
  • Quality Assurance: Ensure subject safety, data integrity, and compliance with relevant regulations and guidelines. Conduct regular quality checks and manage audit initiatives.
  • Communication: Act as a point of contact for assigned deliverables and establish effective project/site level communications.
  • Risk Management: Identify and mitigate risks associated with project deliverables. Monitor site performance and recommend corrective actions.
  • Mentorship: Act as a mentor for junior staff and Technical Solution Specialists.
  • Training: Act as a Subject Matter Expert to support departmental training.
Qualifications
  • Bachelor's degree in life sciences or related field.
  • Minimum of 5 years of relevant experience in clinical trial conduct.
  • Formal or informal leadership experience.
  • Advanced knowledge of clinical trial conduct and applicable clinical research regulatory requirements.
  • Strong written and verbal communication skills.
  • Ability to work on multiple projects and manage competing priorities.
  • Strong organizational, problem-solving, and decision-making skills.
  • Ability to work across cultures and geographies.


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