Clinical Research Associate Specialist

2 days ago


Oslo, Oslo County, Norway IQVIA LLC Full time

As a Clinical Research Associate at IQVIA LLC, you will play a vital role in ensuring the success of clinical trials by performing monitoring and site management tasks.

Key Responsibilities:

  • Conduct site monitoring visits to ensure compliance with study protocols and regulatory requirements.
  • Work closely with sites to adapt and drive subject recruitment plans to meet project needs.
  • Evaluate the quality and integrity of study site practices related to protocol adherence and regulatory compliance.
  • Manage study progress by tracking regulatory submissions, recruitment and enrollment, CRF completion, and data query resolution.

Requirements:

  • Bachelor's degree in a scientific discipline or healthcare preferred.
  • At least 2 years of on-site monitoring experience.
  • Good knowledge of clinical research regulatory requirements, including GCP and ICH guidelines.
  • Strong therapeutic and protocol knowledge, as well as computer skills and communication skills.


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