Clinical Research Coordinator

1 week ago


Reading, Reading, United Kingdom Pharmiweb Full time
Job Overview

As a Clinical Trials Assistant, you will play a crucial role in ensuring the smooth execution of clinical trials. Your primary responsibility will be to provide administrative support to the Clinical Research Associates and Regulatory and Start-Up teams.

Key Responsibilities
  • Assist in maintaining clinical documents and systems, including the Trial Master File (TMF), to ensure site compliance and performance.
  • Prepare, handle, distribute, file, and archive clinical documentation and reports according to standard operating procedures.
  • Review study files for completeness and assist in tracking and managing Case Report Forms (CRFs), queries, and clinical data flow.
  • Act as a central contact for the clinical team for designated project communications, correspondence, and associated documentation.
  • May accompany CRAs on site visits to assist with clinical monitoring duties upon completion of required training.
Requirements
  • High School Diploma or equivalent.
  • 3 years of administrative support experience.
  • Equivalent combination of education, training, and experience.
  • Computer skills, including working knowledge of Microsoft Word, Excel, and PowerPoint.
  • 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 coworkers, managers, and clients.
  • Awareness of applicable clinical research regulatory requirements, including Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.
About IQVIA

IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments, improving patient outcomes and population health worldwide.



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