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CRA II at Precision for Medicine

CRA II role in Belgium with oncology experience.
Remote
Belgium
Undisclosed salary
Precision for Medicine is seeking a CRA II to monitor clinical studies at investigative sites in Belgium. The CRA II will ensure studies are conducted, recorded, and reported per protocol, SOPs, ICH-GCP, and all applicable regulations and standards. This role involves coordinating activities to set up and monitor studies, including identifying investigators, preparing regulatory submissions, and conducting pre-study and initiation visits.
  • Monitoring clinical studies at investigative sites
  • Ensuring studies are conducted, recorded, and reported per protocol
  • Coordinating activities to set up and monitor a study
  • Identifying investigators
  • Preparing regulatory submissions
  • Conducting pre-study and initiation visits
Requirements:
  • College degree or equivalent experience
  • At least 2 years independent on-site monitoring experience within the CRO or Pharmaceutical industry
  • Oncology experience is essential
  • Availability for domestic travel, up to approximately 50-60% travel commitment.
  • Fluency in English and the local language of Belgium
Precision for Medicine offers:
  • A lower than average number of protocols
  • Reasonable travel
  • The chance to have influence and impact
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Precision for Medicine

Precision for Medicine is dedicated to enhancing clinical research and development. They achieve this by providing specialized services that integrate scientific understanding with advanced analytical platforms. They help optimize clinical trials, accelerate drug development, and enable a deeper understanding of disease mechanisms, ultimately aiming to improve patient outcomes through precision medicine approaches and tailored therapeutics.