Experience includes FIH Phase I gene therapy trials, CTIMPS, device studies, commercial and non-commercial and late phase RWE studies. My duties include but are not limited to:-Initiation and management of day to day running of over 30 trials in accordance with Trust Standard Operating Procedures, Good Clinical Practice, Clinical and Research Governance, Data Protection legislation and EU Clinical Trials Directives. -Primary contact with sponsors/CROs in all aspects of budget and contract negotiations. -Liaising with vendors, external subcontractors, private commercial trial units when required-Providing support across a number of research projects and maintaining strong, effective working relationships and communication pathways with clinical and non-clinical teams.-Provide in depth knowledge and administrative support to Investigators and sponsors in regulatory processes for gaining Ethics, MHRA and Trust approvals in line with the National Institute for Health Research (NIHR) Coordinated System for gaining NHS permission to ensure effective and efficient study set up using the Integrated Research Application System.- Responsible for maintaining close links with peripheral hospitals and universities to support the daily management of trials requiring shared care/collaboration.-Development and maintenance of the trial specific drive, ensuring correct versions of protocols, case report forms and patient related materials are available and disseminated to study staff. Keep investigator files, patient source notes/files, spreadsheets, databases and case report forms up to date and audit ready.-Development and implementation of study specific SOPs, training of study team on any processes involved and dissemination of all new relevant research information to staff.- Active lead and participant at team meetings, investigator meetings, ensuring relevant information is disseminated across the wider research team.