clinical research associate Wigan, England
Job description
To be responsible for the management of clinical studies in accordance with the required standards, namely: Medicines for Human Use (Clinical Trials) Regulations; Human Tissue Act; UK General Data Protection Regulations (UK GDPR) and the Data Protection Act, other relevant laws, local Trust policies and procedures. To assist with programmes for recruitment, enrolment, screening and retention of research participants in accordance with the UK Policy for Health and Social care Research; ICH Good Clinical Practice (ICH GCP) guidelines and protocols. To attend MDT meetings, and appropriate clinics, to promote CRN study participation and to screen and recruit new participants, and to act as a resource to the members of the MDT To work with the network Clinical Trials Co-ordinator to facilitate the speedy set up and approval of CRN studies. Complete extensive feasibility assessments of all studies ensuring the Trust has both the capacity and capability to run the research study To ensure all necessary approvals and other agreements are in place prior to commencing the study For further details / informal visits contact: Name Tracey Taylor/Cheryl Finch Job title Senior Research Nurse Managers Email address [email protected] [email protected] Telephone number 01257-256593 01942-822014 Additional contact information In Tracey and Cheryl's absence, please email Alison Robinson, Head of Research [email protected], providing your telephone number to return a call to you.
