Senior Clinical Trials Coordinator

5 days ago


Reading, Reading, United Kingdom Pharmiweb Full time

We are seeking a Clinical Research Associate to support our client sites across the South West of England. As a member of our team, you will have the opportunity to work with a leading global provider of clinical research services and contribute to the success of our clients.

Key Responsibilities
  • Perform site monitoring visits in accordance with contracted scope of work and regulatory requirements.
  • Work closely with sites to adapt, drive, and track subject recruitment plans to enhance predictability.
  • Administer protocol and related study training to assigned sites, establishing regular lines of communication to manage ongoing project expectations and issues.
  • Evaluate the quality and integrity of study site practices, escalating quality issues as necessary.
  • Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution.
Requirements
  • Experience in independent on-site monitoring.
  • Life science degree or equivalent industry experience.
  • Ideal experience in monitoring oncology therapeutic areas but not essential.
  • Flexibility to travel to sites across the South West of England as required.


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