Quick facts

    • France


  • Technology


  • Clinical Research Associate

Apply by: 2023-06-13

In-House Clinical Research Associate (In-House CRA) - Home-based - Japanese-speaking

Published 2023-04-14

What you will do

  • Ensure quality of data submitted from study sites and assure timely submission of data, including appropriate reporting and follow-up for all safety events by site personnel
  • Ensure completeness and compile regulatory documents and ethical submission documentation as appropriate and required (e.g. IRB approval, informed consent, lab certification etc.)
  • Provide applicable updates for site related documentation for filing in the Trial Master File (TMF)
  • Perform feasibility studies/site identification activities for potential sites, as requested
  • What you will bring to the role

  • Excellent interpersonal, oral, and written communication skills in English and local language
  • Ability to contribute to a team remotely
  • Strong customer focus, ability to interact professionally with a sponsor contact
  • Proficiency in Microsoft Office, CTMS, and EDC Systems
  • Your background

  • Four-year college curriculum with a major concentration in life science preferred but not required, OR
  • Two-year college curriculum or equivalent education/training and one year experience with clinical research (e.g. study coordinator, CTA, etc.) or other experience deemed relevant