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Clinical Trial Operations Opportunities at Parexel

Clinical Trial Operations

Initiation Clinical Site Manager II

Job ID 55111BR Buenos Aires, Buenos Aires F.D., Argentina
Working from our office location in Buenos Aires, as an Initiation Clinical Site Manager (ICSM) you will review Site Regulatory Package (SRP) and Informed Consent (ICF) in English and possibly French for site locations throughout North America.

You must have clinical trials experience as a CRA, study nurse or site coordinator ideally with a university degree in a health-related discipline. Understanding of GCP and relevant regulations plus knowledge of submissions and ICF customizations is expected. This is a virtual team environment and your strong interpersonal and communication skills will help you to succeed. Fluency in English is required, preference will be given to those with fluency in French.



Qualifications

  • Significant regulatory experience in clinical trials
  • Educated to degree level preferred (biological science, pharmacy or other health-related discipline preferred), nursing or other relevant qualification/experience
  • Sound awareness of all relevant regulations, including GCP
  • Fluency in English is required

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