Clinical Research Coordinator

1 month ago

London, Greater London, United Kingdom Cyden Ltd Full time
Clinical Trial Assistant Job Description

About the Role

CyDen Ltd is seeking a highly organized and detail-oriented Clinical Trial Assistant to join our dynamic research team in London. As a Clinical Trial Assistant, you will play a crucial role in supporting the planning, coordination, and administration of clinical trials, ensuring they are conducted accurately, efficiently, and in compliance with regulatory and ethical standards.

Key Responsibilities

  • Trial Preparation: Prepare and review all study-related documents before study commencement.
  • Participant Recruitment: Recruit and maintain contact with trial participants throughout the study.
  • Scheduling: Maintain an accurate and up-to-date appointment schedule.
  • Informed Consent: Conduct the informed consent process with all participants.
  • Protocol Adherence: Execute clinical activities according to study protocols, including device treatments, photography, and skin measurements.
  • Data Management: Ensure complete and accurate Case Report Form (CRF) entries during trials and transcription of raw data.
  • Patient Monitoring: Monitor and report patient status, safety, adverse events, and device effects.
  • Inventory Management: Monitor clinical suite supplies and replenish as needed.
  • SOP Development: Assist in creating and updating Standard Operating Procedures.
  • Quality Control: Promptly address and report concerns arising during studies and maintain utmost confidentiality.

Requirements

  • Education: Bachelor's degree in life sciences, healthcare, or related field; clinical research certification is a plus.
  • Skills:
    • Strong attention to detail and organizational abilities.
    • Excellent written and verbal communication skills.
    • Proficiency with Microsoft Office Suite and clinical trial management systems (CTMS).
    • Ability to work independently and collaboratively in a fast-paced environment.
  • Ideal Experience:
    • Experience: 1-3 years in clinical research or a related field; previous experience with clinical trial documentation or administration preferred.
    • Familiarity with GCP guidelines, ICH regulations, and regulatory submission processes.

What We Offer

CyDen Ltd offers a dynamic, fast-paced environment with a supportive and welcoming team culture. We provide extensive resources and training to ensure your success in this role. If you are a detail-oriented and organized individual with a passion for clinical research, we encourage you to apply for this exciting opportunity.

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