Clinical Trial Specialist

2 days ago


Oslo, Oslo County, Norway IQVIA Argentina Full time
Job Description

The Clinical Research Associate will be accountable for managing the progress of assigned studies, including tracking regulatory submissions, recruitment, and data query generation. They will also be responsible for maintaining documentation regarding site management and monitoring visit findings.

Qualifications
  • Bachelor's degree in a scientific discipline or health care preferred.
  • At least 2 years of on-site monitoring experience.
  • Good knowledge of clinical research regulatory requirements and therapeutic knowledge.


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