Clinical Research Coordinator

4 weeks 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 our 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 Clinical Research Associates and Regulatory and Start-Up teams with updating and maintaining clinical documents and systems, including the Trial Master File.
  • Prepare, handle, distribute, file, and archive clinical documentation and reports according to standard operating procedures.
  • Assist with periodic review of study files for completeness.
  • Assist Clinical Research Associates and Regulatory and Start-Up teams with preparation, handling, and distribution of Clinical Trial Supplies and maintenance of tracking information.
  • Track and manage Case Report Forms, queries, and clinical data flow.
  • Act as a central contact for the clinical team for designated project communications, correspondence, and associated documentation.
  • May accompany Clinical Research Associates on site visits to assist with clinical monitoring duties upon completion of required training.
Requirements
  • High School Diploma or equivalent required.
  • 3 years of administrative support experience.
  • Equivalent combination of education, training, and experience.
  • Computer skills, including working knowledge of Microsoft Word, Excel, and PowerPoint.
  • Written and verbal communication skills, including good command of the English language.
  • Effective time management and organizational skills.
  • Ability to establish and maintain effective working relationships with coworkers, managers, and clients.
  • Awareness of applicable clinical research regulatory requirements, including Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.
  • Knowledge of applicable protocol requirements.
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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