Anna Attwood

WORK HISTORY

EDUCATION

ABOUT ANNA ATTWOOD

My role in the CTM team at Perspectum provided me with a great base for a future in clinical research. I have up-to-date GCP training and have been trained to work with patient identifiable information.I have been involved in various stages of REC approved, sponsored studies including; preparing documents for ethics submission (protocols/patient facing documentation), relationship building with collaborators, submitting study ethics, study set up, management (budgeting, recruitment tracking, monitoring) and close out. I have also worked with collaborators where Perspectum\'s MRI technology has been utilised in external research. This project management-style role saw me maintain key relationships, manage contracting and budgets, set up sites for scanning and follow internal processes to allow smooth flow of data from collaborators to our analysis team and back.While at Perspectum, and aside from my work in the CTM team, I was also heavily involved in the set up of our laboratory space (including an application for a HTA licence), as well as the initiation of the x-ray service for the Oxford CDC working alongside Oxford University Hospitals Medical Physics Team, creating all new processes and documentation to ensure compliance to IR(ME)R and IRR regulations.I have previous experience as a Senior Scientist with a demonstrated history of working on both immuno-oncolocy and autoimmune based projects where I was proficient in the design, execution, analysis and reporting of complex, and often novel, immuno-assays. I have practical experience in the range of laboratory techniques including cell culture, flow cytometry, cell separation and isolation, Luminex, ELISA, IncuCyte, TR-FRET and various other immuno-assays.I held the position of Radiation Protection Supervisor in a laboratory setting and now with further experience in the initiation of an x-ray service, I am familiar with both IRR and IRMER regulations.