Agile Diabetes and Endocrine Clinical Research Nurse

Duties and Responsibilities Clinical and Communication Responsibilities • Manage a caseload of participants acting as a professional in ensuring a duty of care to the participant and their families. • Work within relevant regulations and ICH GCP (International Conference on Harmonisation and Good Clinical Practice), Trusts policies, research governance, Medicines for Human Use (Clinical Trials Regulations) Regulations, Data Protection Act and Human Tissue Act. • ensuring that the clinical trial protocol is adhered to at all times. • Devise, implement and evaluate strategies for identifying eligible participants for research studies, including by attending clinics, departments, screening notes/consultant referral and Multidisciplinary Team (MDT) meetings. • Participate in the informed consent process acting as a resource and support to participants and their families. For appropriate studies take informed consent and ensure on-going consent in accordance with the necessary Trust research governance arrangements and necessary competent regulatory authority Regulations and International Conference on Harmonisation of Good Clinical Practice (ICH GCP) Job description Job responsibilities Duties and Responsibilities Clinical and Communication Responsibilities • Manage a caseload of participants acting as a professional in ensuring a duty of care to the participant and their families. • Work within relevant regulations and ICH GCP (International Conference on Harmonisation and Good Clinical Practice), Trusts policies, research governance, Medicines for Human Use (Clinical Trials Regulations) Regulations, Data Protection Act and Human Tissue Act. • ensuring that the clinical trial protocol is adhered to at all times. • Devise, implement and evaluate strategies for identifying eligible participants for research studies, including by attending clinics, departments, screening notes/consultant referral and Multidisciplinary Team (MDT) meetings. • Participate in the informed consent process acting as a resource and support to participants and their families. For appropriate studies take informed consent and ensure on-going consent in accordance with the necessary Trust research governance arrangements and necessary competent regulatory authority Regulations and International Conference on Harmonisation of Good Clinical Practice (ICH GCP)