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Medicine & Social Care

Clinical Research Associate

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Description of job position

  • Conducting monitoring visits to clinical trial sites to ensure compliance with study protocols, regulatory requirements, and Good Clinical Practice (GCP).
  • Reviewing and verifying study documentation including informed consent forms, source documents, and case report forms.
  • Collaborating with site staff to facilitate the smooth execution of clinical trials.
  • Providing training and support to site personnel on study protocols and procedures.
  • Identifying and resolving issues related to study conduct and data integrity.
  • Collecting and reporting adverse events and serious adverse events in accordance with regulatory guidelines.
  • Maintaining accurate and timely records of monitoring activities and findings.
  • Assisting in the preparation of study-related materials, including monitoring plans and reports.
  • Ensuring proper storage and handling of investigational products.
  • Participating in project team meetings and contributing to study progress discussions.

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