Stand by, we'll show you...
Once you understand the requirements outlined in the advert, please ensure your application clearly reflects where you match them including any examples you would like to highlight.
The post holder will play a key role in the development and delivery of research projects at the Trust, enabling the Trust to grow its research business. You will join a team involved in the provision and maintenance of systems, Standard Operating Procedures (SOPs) and advice to ensure high quality research performance and compliance with relevant regulations. You will be involved in reviewing and advising on project design, ethical and Health Research Authority (HRA) application/approval processes, contract arrangements, essential documents, clinical trial planning, safety reporting, GCP monitoring and audit as well as providing relevant training and advice related to clinical research throughout the organisation. You will support the set-up and initiation of research projects within the Trust, ensuring sound contractual and financial arrangements; and in accordance with the relevant national and local regulatory frameworks and national research timelines and performance targets. The role encompasses all aspects of non-commercial and commercial research which is mainly multi-centred National Institute of Health Research (NIHR) portfolio.
For further information, please see the attached trust job description and person specification for a full list of duties and responsibilities.
Once you understand the requirements outlined in the advert, please ensure your application clearly reflects where you match them including any examples you would like to highlight.
The post holder will play a key role in the development and delivery of research projects at the Trust, enabling the Trust to grow its research business. You will join a team involved in the provision and maintenance of systems, Standard Operating Procedures (SOPs) and advice to ensure high quality research performance and compliance with relevant regulations. You will be involved in reviewing and advising on project design, ethical and Health Research Authority (HRA) application/approval processes, contract arrangements, essential documents, clinical trial planning, safety reporting, GCP monitoring and audit as well as providing relevant training and advice related to clinical research throughout the organisation. You will support the set-up and initiation of research projects within the Trust, ensuring sound contractual and financial arrangements; and in accordance with the relevant national and local regulatory frameworks and national research timelines and performance targets. The role encompasses all aspects of non-commercial and commercial research which is mainly multi-centred National Institute of Health Research (NIHR) portfolio.
For further information, please see the attached trust job description and person specification for a full list of duties and responsibilities.
Please wait...this will take a moment...
