Study Monitor

3 days ago

Swansea, City and County of Swansea, United Kingdom Cyden Ltd Full time
Job Title: Study Monitor

We are seeking a highly skilled Study Monitor to join our Clinical and Application Research Team at Cyden Ltd. The successful candidate will be responsible for overseeing the progress of clinical and application research/trials, ensuring 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 required essential documents for study start-up and throughout the conduct of a trial.
  • Conduct on-site training and motivate investigators.
  • Verify patient data and ensure adherence to protocol, GCP, and internal SOPs.
  • Maintain all files pertaining to 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 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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