Clinical Research Coordinator

4 weeks ago


Shanghai, Shanghai, China IQVIA Full time
Responsibilities

As a Clinical Trial Coordinator at IQVIA, you will be responsible for:

  • Tracking and reporting essential documents
  • Ensuring collation and distribution of study tools and documents
  • Preparing documents and correspondence
  • Collating, distributing/shipping, and archiving clinical documents
  • Assisting with eTMF reconciliation and executing the eTMF Quality Control Plan
  • Collaborating with other country roles to provide and collect forms/lists for site evaluation/validation, site start-up, and submissions
  • Obtaining, tracking, and updating study insurance certificates
  • Developing, controlling, updating, and closing-out country and site budgets
  • Negotiating, approving, and maintaining contracts
  • Tracking and reporting contract negotiations
  • Calculating and executing payments to investigators, vendors, and grants
  • Maintaining tracking tools and ensuring adherence to financial and compliance procedures
About IQVIA

IQVIA is a leading global provider of advanced analytics, technology solutions, and clinical research services to the life sciences industry. We believe in pushing the boundaries of human science and data science to make the biggest impact possible – to help our customers create a healthier world.



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