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Thermo Fisher Scientific·3 days ago
3 days ago

CRA (Level I)

Buenos Aires, ArgentinaFull-timeMid · 2-5 years

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About this role

Join us as a Clinical Research Associate (Level I) and play a key role in monitoring clinical trials, ensuring protocol and regulatory compliance. You will manage site processes, conduct site visits, and support data integrity. Ideal for candidates with clinical research experience and strong monitoring skills.

Skills

  • clinical monitoring
  • ich-gcp compliance
  • risk based monitoring
  • sdr
  • sdv
  • crf review
  • site management
  • clinical trial management system
  • root cause analysis
  • problem solving
  • medical terminology
  • regulatory compliance
  • investigational product assessment
  • trial close out
  • investigator site initiation
  • essential document management
  • business writing
  • project reporting
  • process improvement
  • presentation skills
  • team collaboration
H1B sponsor likely
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