Research Associate Location: Manchester, UK Work Setting: Site-based / UK travel Employment Type: Full-time Industry: Clinical Research / Life Sciences Function: Clinical Operations / Research Visa Sponsorship: Not available About the Role An international clinical research organisation is seeking a Research Associate to support Oncology clinical trials across UK sites. The role involves independent site monitoring and close collaboration with investigators and study teams throughout the trial lifecycle. Key Responsibilities

  • Conduct site selection, initiation, monitoring and close-out visits in line with GCP.
  • Support site recruitment plans and study delivery.
  • Provide protocol and study training to assigned sites.
  • Monitor site quality, data integrity and regulatory compliance.
  • Track regulatory submissions, recruitment, CRF completion and data queries.
  • Maintain TMF/ISF documentation in accordance with GCP requirements.
  • Document monitoring findings, action plans and follow-up activities.
  • Collaborate with study teams and sites to resolve issues and maintain project progress. Requirements
  • Experience conducting independent on-site monitoring in Oncology, preferably on unblinded studies.
  • Strong knowledge of GCP and ICH guidelines.
  • Life science degree or equivalent clinical research industry experience.
  • Willingness and flexibility to travel to UK sites. Note: This position is not eligible for visa sponsorship.

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