Role and Responsibilities

• ** Keep the commercial success of the site forefront in mind without compromising patient care.**
• Manage nursing activities relating to clinical trials, from startup to close out, adhering to ICH/GCP guidelines.
• Drive quality assurance measures and implement appropriate policies to enhance clinical research activity and ensure successful business delivery.
• Exercise meticulous attention to detail when collecting, recording, safety reporting, and verifying study data.
• Monitor trends and share best practice within the team.
• Promote a professional, welcoming, and pleasant environment for staff and participants to ensure effective team collaboration.
• Provide professional leadership to foster a positive working culture.
• Facilitate communication by participating in regular:
  • Clinical team meetings
  • Multidisciplinary meetings
  • Project strategy meetings
  • Feasibility assessments
  • Core study meetings
• Review research protocols and coordinate training and education requirements for clinical staff.
• Attend:
  • Pre-study site selection visits
  • Site initiation visits for new studies
  • Updates on changes in study protocols
• Conduct patient interest visits (chats) effectively, demonstrating knowledge and understanding of the study protocol.
• Optimise patient retention by keeping participants engaged throughout the study.
• Ensure the clinical team regularly checks the emergency trolley and takes the lead on initiating emergency procedures, including:
  • Cardiac arrest management
  • Anaphylaxis response
  • Fire incidents
  • Critical incident response
• Oversee laboratory activities and have the capability to conduct laboratory duties as required per study terms.