Clinical Trials Coordinator

The main purpose of the role is to provide comprehensive data management and administrative support to the Lung Clinical Trials Team according to Good Clinical Practice (GCP), standard operating procedures (SOPs) and Trust policies., The post holder will:

• Manage and maintain the clinical trials database.
• Assist with the efficient and timely set up of clinical trials.
• Assist with the tracking and raising of invoices.
• Provide support with maintenance and quality assurance of all trial related documentation in accordance with relevant legislation and guidelines.
• Assist with preparation for audit and inspections within assigned teams.
• General trial-related communication in accordance with the Data Protection Act.
• Assist with maintenance of clinical trial documentation.
• Manage own workload for daily trial activity including case report form completion and amendment processing to meet internal and external deadlines
  
  The successful post holder will have experience working within clinical trial delivery within an NHS site and preferably an understanding of oncology research.
  
  The Christie Lung Cancer Research Team vision is to build upon our reputation as a local and national leader in clinical trial delivery. Pursuing exemplary care and prioritising the safety and experience of our clinical research participants, carried out by a highly trained and passionate clinical research team.
By becoming a member of the Lung Research Team, you will be joining a dynamic and supportive team who are constantly striving to improve ourselves by work collaboratively across the nursing, medical and administrative teams. We are a team that strives to develop our staff to the best of their potential and are keen for all members of our team to continue to learn and share knowledge. I would strongly encourage interested applicants to contact the team to further discuss the roles and how you can become a key member of this exemplary team.