Clinical Research Coordinator

1 day ago


Swansea, City and County of Swansea, United Kingdom Cyden Ltd Full time
{"title": "Study Monitor", "description": "Job Summary

Cyden Ltd is seeking a highly skilled Study Monitor to oversee the progress of clinical and application research/trials. The successful candidate will ensure all research is conducted, recorded, and reported in accordance with Protocols, SOPs, ICH-GCP and applicable regulatory requirements.

Key Responsibilities

  • Provide a global evaluation of all investigations commissioned and executed.
  • Ensure collection of the required essential documents for study start-up and throughout the conduct of a trial.
  • Conduct on-site training and motivate the investigators.
  • Verify patient data and ensure adherence to protocol, GCP and internal SOPs.
  • Maintain all files pertaining to the clinical trials, track study progress and ensure timely quality updates are provided.
  • Perform routine site visits and assessments.

Requirements

  • Strong interest in clinical trial and application research.
  • Experience of working in a similar role.
  • Excellent organisational, planning, and interpersonal skills.
  • Ability to work under pressure and demonstrate initiative and problem-solving skills.
  • Knowledge of clinical trials regulations, ICH-GCP and excellent literacy, numeracy, and IT skills.

What We Offer

Cyden Ltd is a dynamic and innovative company that offers a challenging and rewarding work environment. The successful candidate will have the opportunity to work with a talented team of professionals and contribute to the success of our clinical and application research team.

"}

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