Matthew Trivett

Background

About Matthew Trivett

Motivated and hardworking Regulatory Affairs Professional specialising in Medical Devices with 4 years experience in the clinical trials arena holding positions in Regulatory Affairs, Clinical Trial co-ordination, Clinical Trial Pharmacy and R&D.Currently working in the CRO setting with experience in: Medical Device Clinical Trial Application across several countries within the EU, assisting with Regulatory strategy and ensuring studies adhere to relevant Directives and Legislation, co-ordination of multiple site studies, assisting CRAs with monitoring and site management. Meticulous and able to work under pressure accurately to tight deadlines. Uses own initiative to address and resolve problems. Excellent organisational and time management skills with ability to forward plan and prioritise own workload in order to ensure key tasks are completed to set deadlines across several projects. Strong team work and communication skills successfully contributing towards various aspects of the clinical trial process. Effectively worked with academics and healthcare professionals to co-ordinate a range of clinical research projects and complete Regulatory submissions.Scientific background gaining MEng qualification in Biochemical Engineering from University College London.Hardworking with a strong can do attitude towards new challenges.Therapeutic areas: Medical Device, Cardiac - Stent, Gastroenterology - IBSContact Details: email: Matthew.trivett1@gmail.com, phone: 07765197494