Clinical Trials Associate

Remote
Clinical – Regulatory /
Full Time /
Remote

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Regulatory

  • How many years of experience creating and maintaining regulatory binders and all other essential documents do you have?
  • How many years of experience facilitating the submission and training of clinical trial protocols, amendments, and informed consent documents do you have?
  • Have you worked as a Clinical Research Coordinator?
  • How many years of study start up experience do you have?
  • What Ereg , QMS, and Clinical Trial Management Systems are you proficient in?
  • Where are you located?
  • What is your desired compensation?