Senior Clinical Research Practitioner

As a Research Practitioner, you will be expected to use an in depth knowledge of trial protocols and their application in practice, alongside a working knowledge and compliance with the local, national and international research regulations. Delivery of recruitment targets in line with the contractual agreements and agreed time lines. In conjunction with the line manager, be responsible for maintaining a balanced portfolio. Open and manage allocated projects, set timescales and resolve problems. This includes management of the set up process. Take responsibility for all areas of practice relating to the conduct of clinical trials and research studies. Maintain accurate records of portfolio activities. Resolve issues, any breaches and protocol deviations. Report Adverse Events (AEs) using appropriate procedures, including the expedited reporting of Serious Adverse Events (SAEs) and Suspected Unexpected Serious Adverse Reactions (SUSARs).