Stand by, we'll show you...
The Cancer Clinical Trials Unit at UCLH is looking to recruit a Data Manager to support a portfolio of Phase II-III clinical trials in the Leukaemia and Non-Malignant Haematology clinical trials team. You may be required to cover other disease areas on a short-term or longer term basis.
The post-holder will be required to deliver and verify trial-specific information to sponsors, support the team with the set-up of new clinical trials and assist as needed with the processing of biological samples, amongst other tasks. You will be part of supportive and dynamic team, working closely with clinical research staff. Whilst the position is administrative, the role is vital in supporting clinical research staff deliver excellent care to patients with cancer.
We are currently supporting hybrid remote working, allowing a combination of working from home and office-based working. Flexibility around on-site working is essential and you may be required to attend the office at relatively short notice to ensure that the service is covered.
We ideally want someone with experience of clinical research, knowledge of cancer, good verbal and written communication skills and some experience of working in a healthcare setting. However, if you have some of these criteria and clear enthusiasm for the role, we welcome your application.
This advert will now close on 03/11/2024 at midnight.
The post holder will:- Have a portfolio of trials for which they are responsible- Complete data entry into case report forms for assigned trials as per protocols- Ensure case report forms are completed are of high quality, accurate and sent in a timely manner- Resolve issues with source data and anomalous data at the time of reporting, reviewing against previously reported data as well as local and national normal ranges.- Prioritises workload to manage time effectively- Process updated information and documents for the successful running of the study- Create and maintain both paper and electronic trial site files- Maintain list/database of up-coming, current and recently closed clinical trials- Maintain electronic and paper list of accrual to trials- Organise and prepare documentation for audits and monitoring visits.- Process biological samples in the trials lab- Liaise with the MDT, Principal and Sub Investigators, Sponsors, and support departments professionally and appropriately- Obtain tumour block samples- Upload scans as required by trial protocol- Escalate issues to senior team members
About us
For the full Person Specification and more information regarding the main responsibilities of this role, please refer to the attached Job Description.
The portfolio is very diverse, with a wide range of studies, to reflect the varied nature of the disease areas, with multiple trials for different subtypes of acute and chronic leukaemias, sickle cell disease and thalassemia. The successful applicant should be organised, pro-active, with strong attention to detail and able to work autonomously, while also collaborating and communicating with the rest of the trials team and the doctor. Full duties are explained in the attached job description.
Come and be a part of the best NHS trust in England to work for, according to our staff*
UCLH top trust to work at in England for the second year running! : University College London Hospitals NHS Foundation Trust
*In the most recent NHS staff survey UCLH had the highest percentage of staff who said they would recommend us as a place to work, out of all general acute or acute/community NHS trusts in England for the second year in a row.
UCLH top trust to work at in England for the second year running! University College London Hospitals NHS Foundation Trust.
Once again, UCLH has received the highest score of all general acute and acute/community NHS trusts in England for staff that would recommend us as a place to work.
The Cancer Clinical Trials Unit at UCLH is looking to recruit a Data Manager to support a portfolio of Phase II-III clinical trials in the Leukaemia and Non-Malignant Haematology clinical trials team. You may be required to cover other disease areas on a short-term or longer term basis.
The post-holder will be required to deliver and verify trial-specific information to sponsors, support the team with the set-up of new clinical trials and assist as needed with the processing of biological samples, amongst other tasks. You will be part of supportive and dynamic team, working closely with clinical research staff. Whilst the position is administrative, the role is vital in supporting clinical research staff deliver excellent care to patients with cancer.
We are currently supporting hybrid remote working, allowing a combination of working from home and office-based working. Flexibility around on-site working is essential and you may be required to attend the office at relatively short notice to ensure that the service is covered.
We ideally want someone with experience of clinical research, knowledge of cancer, good verbal and written communication skills and some experience of working in a healthcare setting. However, if you have some of these criteria and clear enthusiasm for the role, we welcome your application.
This advert will now close on 03/11/2024 at midnight.
The post holder will:- Have a portfolio of trials for which they are responsible- Complete data entry into case report forms for assigned trials as per protocols- Ensure case report forms are completed are of high quality, accurate and sent in a timely manner- Resolve issues with source data and anomalous data at the time of reporting, reviewing against previously reported data as well as local and national normal ranges.- Prioritises workload to manage time effectively- Process updated information and documents for the successful running of the study- Create and maintain both paper and electronic trial site files- Maintain list/database of up-coming, current and recently closed clinical trials- Maintain electronic and paper list of accrual to trials- Organise and prepare documentation for audits and monitoring visits.- Process biological samples in the trials lab- Liaise with the MDT, Principal and Sub Investigators, Sponsors, and support departments professionally and appropriately- Obtain tumour block samples- Upload scans as required by trial protocol- Escalate issues to senior team members
About us
For the full Person Specification and more information regarding the main responsibilities of this role, please refer to the attached Job Description.
The portfolio is very diverse, with a wide range of studies, to reflect the varied nature of the disease areas, with multiple trials for different subtypes of acute and chronic leukaemias, sickle cell disease and thalassemia. The successful applicant should be organised, pro-active, with strong attention to detail and able to work autonomously, while also collaborating and communicating with the rest of the trials team and the doctor. Full duties are explained in the attached job description.
Come and be a part of the best NHS trust in England to work for, according to our staff*
UCLH top trust to work at in England for the second year running! : University College London Hospitals NHS Foundation Trust
*In the most recent NHS staff survey UCLH had the highest percentage of staff who said they would recommend us as a place to work, out of all general acute or acute/community NHS trusts in England for the second year in a row.
UCLH top trust to work at in England for the second year running! University College London Hospitals NHS Foundation Trust.
Once again, UCLH has received the highest score of all general acute and acute/community NHS trusts in England for staff that would recommend us as a place to work.
Please wait...this will take a moment...
