Start Date
Immediate
Expiry Date
13 Apr, 25
Salary
29114.0
Posted On
14 Jan, 25
Experience
0 year(s) or above
Remote Job
No
Telecommute
No
Sponsor Visa
No
Skills
Good communication skills
Industry
Pharmaceuticals
Ensure that all reports produced are accurate, timely and presented in a user friendly manner. To work closely with the Trust IT department on these issues when needed. To routinely audit data quality on the manual and electronic systems within the department to ensure high standards that comply with Trust and external governing bodies requirements. To monitor performance against the data quality targets taking remedial action where necessary.
To take responsibility for data security and integrity. To establish back up systems for data within the department that will comply with Trust systems. To ensure that the databases and the data collection systems comply with confidentiality, Caldicott and data protection, and all other relevant (Trust and non Trust) policies and procedures. To liaise regularly with counterparts nationally to ensure that there is consistency of approach in data collection to facilitate audit across the centres in the UK.
To represent the unit at relevant data management conferences, in the UK or on a European basis. To keep up to date with developments in data collection for this service on a European basis through such liaison with colleagues. To liaise with the suppliers of data base systems where appropriate regarding maintenance, requests for technical support and advice and database development. To assist in the development of other database /information systems.
To be responsible for the collection of data relating to patients treated within the department, in particular, where the patient is entered onto a clinical trial. Act as a point of contact for regional, national and international data queries. Ensure that Trust policy regarding Data Protection is adhered to. Assist the Trial Coordinator in all aspects of maintaining records of patients on trials and the regulatory issues that govern the management of clinical trials.
Provide administrative support when needed. As a flexible working friendly organisation, we want to be sure that you can work in a way that is best for us and for our patients, and for you. Speak to us about how we might be able to accommodate a flexible working arrangement. If it works for the service, we will do our best to make it work for you
Please refer the Job description for details