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Clinical Protocol Support Specialist

2 months ago

Bethesda, Gwynedd, United Kingdom PriceSenz Full time

Job Summary

We are seeking a highly organized and detail-oriented Clinical Protocol Support Specialist to join our team at PriceSenz. The successful candidate will provide administrative support to our research team, ensuring the smooth operation of clinical trials.

Key Responsibilities

  • Assist researchers in the development, assembly, and review of clinical trial documents.
  • Develop and maintain trial-related documents and operational procedures.
  • Maintain study databases and conduct basic analysis.
  • Assist researchers in collecting, distributing, and filing regulatory documents.
  • Provide technical support to researchers and the clinic.

Requirements

  • Masters degree in a relevant field.
  • Previous experience in clinical trial work, electronic medical records, and protocol review and revision.
  • Excellent communication and organizational skills.

Field of Study

  • Neuroscience.

Why Join Us

At PriceSenz, we offer a dynamic and supportive work environment, with opportunities for professional growth and development. If you are a motivated and detail-oriented individual with a passion for clinical research, we encourage you to apply for this exciting opportunity.