Clinical Trial Operations Specialist

hace 18 horas


Madrid, Madrid, España Iqvia Argentina A tiempo completo
Job Description

In this role, you will oversee the local management of clinical trials in Iqvia Argentina. As a key member of our team, you will be responsible for ensuring the successful execution of trial protocols, managing local trial teams, and delivering high-quality data and trial documents.

Key Responsibilities:
  • Operational oversight of assigned protocol(s) at the country level from start-up through to database lock and closeout activities.
  • Ensure local trial teams deliver quality data and trial documents compliant with clinical trial protocol, company SOPs, ICH-GCP, and regulatory requirements.
  • Collaborate with central study team and local stakeholders to select sites for participation in trials.
  • Provide input to study-level documents and lead/co-coordinate local team activities in compliance with SOPs and regulations.
  • Develop local trial-specific procedures and tools, recruitment planning, contingency and risk management, and budget forecasting.
  • Maintain and update trial management systems, using study tools and management reports available to analyze trial progress.
Requirements:
  • Bachelor's degree in a life science or related field.
  • Prior experience in clinical trial management or a related field.
  • Strong knowledge of clinical trial regulations, SOPs, and GCP guidelines.
  • Excellent communication and project management skills.
  • Ability to work effectively in a team environment.
Salary and Benefits:

We offer an attractive salary of $75,000 - 90,000 USD per annum, depending on experience. Our benefits package includes comprehensive health insurance, paid time off, and opportunities for professional growth and development.



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