Clinical Trial Coordinator

2 days ago


Sutton Coldfield, Birmingham, United Kingdom The Royal Marsden Full time
Job Overview

We are seeking a highly organized and detail-oriented Clinical Trial Administrator to join our Sutton-based Haemato-Oncology department.

Main Responsibilities

The successful candidate will be responsible for:

  • Supporting clinical research teams with study administration, ensuring the efficient and successful delivery of clinical trials and other studies according to Good Clinical Practice (GCP), standard operating procedures (SOPs), Trust policies, and all applicable regulations and governance.
  • Ensuring timely and accurate entry of data and relevant information into appropriate database systems for trials across both our research locations (Chelsea and Sutton).
  • Assisting the Research Nurses with the prompt resolution of data queries.
  • Providing support to the clinical research team in the daily trials activity and assisting in workload management.
Key Skills and Qualifications

The ideal candidate will possess:

  • A good understanding of medical terminology.
  • Experience in working with databases.
  • Excellent communication, administrative, and IT skills.
  • A flexible approach to duties and the ability to work both as part of a team and independently.
Person Specification

The successful candidate will have:

  • Education to at least GCSE/A level.
  • Knowledge of ICH/GCP guidelines (desirable).
  • Previous experience of working in the NHS or for an oncology trials unit (desirable).
About The Royal Marsden

The Royal Marsden is a world-leading cancer centre, committed to delivering exceptional patient care and pioneering new treatments. We value diversity and are committed to the recruitment and retention of underrepresented minority groups.



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