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Clinical Research Coordinator

2 months ago

Beijing, Beijing, China IQVIA Full time
Job Overview

As a key member of our clinical research team, you will play a vital role in ensuring the successful delivery of clinical trials. Your primary responsibility will be to provide administrative support to our Clinical Research Associates and Regulatory and Start-Up teams, ensuring that all clinical documents and systems are accurately updated and maintained.

Key Responsibilities
  • Assist in the preparation, handling, and distribution of clinical documentation and reports, ensuring compliance with standard operating procedures.
  • Collaborate with the clinical team to track and manage Case Report Forms (CRFs), queries, and clinical data flow.
  • Act as a central point of contact for clinical team communications, correspondence, and associated documentation.
  • Support the preparation and handling of Clinical Trial Supplies, maintaining accurate tracking information.
  • Assist with the review of study files for completeness and accuracy.
Requirements
  • High School Diploma or equivalent required.
  • 3 years of administrative support experience.
  • Excellent computer skills, including Microsoft Office Suite.
  • Strong written and verbal communication skills, with a good command of the English language.
  • Effective time management and organizational skills.
  • Ability to establish and maintain effective working relationships with colleagues, managers, and clients.
  • Awareness of applicable clinical research regulatory requirements, including Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.

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 a meaningful impact – to help our customers create a healthier world.