Research Data Administrator

Job summary

To be responsible for the entry of all allocated trial related electronic data capture systems in compliance with the trial protocol.

To be responsible for the input of clinical and other data necessary for clinical trial purposes Checking all data is accurately populated, ensuring all empty data fields are completed to ensure data quality, completeness, validity, consistency, timeliness and accuracy to ensure the data is appropriate for its specific use within the study

Maintain and update Databases used for all aspects of the patient pathway experience within Portfolio clinical research studies. This includes Microsoft Excel, and on line web databases.

Maintain spread sheets/database on patient recruitment.

Responsible for the inputting data into EDGE 'Intelligent Research Management system' Extract data from information systems and prepare summaries to support regular clinical audit, update reports as requested.

Responsible for forwarding completed data and data queries to trials unit (or sponsor). Maintenance of robust systems to track and monitor patient and financial progress through clinical trials.

Main duties of the job

Maintain and update Databases used for all aspects of the patient pathway experience within Portfolio clinical research studies. This includes Microsoft Excel, and on line web databases.

Maintain spread sheets/database on patient recruitment.

Responsible for the inputting data into EDGE 'Intelligent Research Management system' Extract data from information systems and prepare summaries to support regular clinical audit, update reports as requested.

Responsible for forwarding completed data and data queries to trials unit (or sponsor). Maintenance of robust systems to track and monitor patient and financial progress through clinical trials.

To be responsible for the electronic Case Report Forms (CRFs) in line with the agreed timelines within the Clinical Trial Agreement (CTA) for sponsors.

To be responsible for liaising with Clinical Trials Units (Sponsor) regarding data queries and for checking/resolving data queries.

To be responsible for liaising with research nurses and commercial trial sponsors to ensure complex data issues are resolved.

To have a basic understanding of the activities associated with each trial that is allocated to the post holder eg financial processes & implications of data entry delay or inaccuracy.

To utilise the Trust's IT systems eg: Mosaiq; Maxims; Order Comms; EPRO, etc in order to access relevant information for trial data collection purposes.

Uploading of digital images required by sponsors.

About us

As an organisation, the NHS offers a wide range of benefits including flexible working, fantastic pension contributions, market leading annual leave allowance, career progression and regular conversations, not to mention our Blue Light Card and NHS exclusive discounts.The benefits of working in Somerset include the idyllic countryside, with our areas of outstanding beauty and stunning coastlines. You will get to enjoy these perks whilst still only being a stone's throw away from bustling city centres like Bristol, Bath and Exeter and only two hours away from London.There are excellent educational facilities in the area and, when compared to other regions, house prices are reasonable. You will to experience the best of both in Somerset, the countryside and the cosmopolitan -- there is truly something for everyone!