Clinical Research Associate II

3 weeks ago


Kirkland, Quebec, Canada IQVIA Full time
Job Summary:

IQVIA Biotech is seeking a Clinical Research Associate II with expertise in oncology monitoring to join our team in Eastern Canada.

Responsibilities:
  • Participate in the preparation and execution of Phase I-IV clinical trials.
  • Oversee the progress of clinical investigations by conducting site evaluation, initiation, and interim close-out visits to sites.
  • Monitor clinical trials in accordance with Good Clinical Practices and procedures set forth by IQVIA Biotech and sponsors.
  • Collaborate with the Clinical Trial Manager (CTM) and/or Lead CRA to ensure all monitoring activities are conducted according to study requirements.
Requirements:
  • BS/BA/BSc (or equivalent) in one of the life sciences or health care background (RPh, RN, etc.) and a minimum of two (2) years of monitoring/site management experience.
  • Must possess 2+ years of oncology and/or medical device experience.
  • Experience in monitoring and/or coordinating clinical trials required.
  • Must be able to travel domestically approximately 65%-85%.
  • Valid driver's license.
What We Offer:

IQVIA is a leading global provider of advanced analytics, technology solutions, and clinical research services to the life sciences industry. We believe in pushing the boundaries of human science and data science to make the biggest impact possible – to help our customers create a healthier world.



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