Clinical Research Coordinator

1 month ago


Shanghai, Shanghai, China IQVIA Full time
Job Summary

We are seeking a highly organized and detail-oriented Clinical Trial Coordinator to join our team at IQVIA. As a Clinical Trial Coordinator, you will be responsible for ensuring the smooth execution of clinical trials, from trial and site administration to document management and regulatory compliance.

Key Responsibilities
  • Manage trial and site administration, including tracking and reporting, collation and distribution of study tools and documents, and updating clinical trial databases.
  • Coordinate clinical supply and non-clinical supply management, in collaboration with other country roles.
  • Prepare and manage documents and correspondence, including preparing documents for investigator meetings and ensuring compliance with regulatory requirements.
  • Support regulatory and site start-up responsibilities, including providing and collecting forms and lists for site evaluation and validation, and obtaining and tracking study insurance certificates.
  • Collaborate with finance and budgeting representatives to develop country and site budgets, track and report negotiations, and ensure compliance with financial procedures.
  • Organize meetings and support local investigator meetings, including preparing materials and selecting venues.
Requirements
  • Bachelor's degree in Life Science or equivalent healthcare experience.
  • Minimum 1-2 years of experience in clinical research or relevant healthcare experience.

We offer a dynamic and supportive work environment, with opportunities for professional growth and development. If you are a motivated and detail-oriented individual with a passion for clinical research, we encourage you to apply for this exciting opportunity.



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