circa £38,600 pa depending on experience
Flexible working and benefits. Full time 35 hours per week. 2-year fixed term contract.
Based in our office in London or home based (with regular travel to office)
The UK Cystic Fibrosis Registry is a database of consenting people with cystic fibrosis across the UK collecting demographic, clinical care, and health outcomes data from clinical teams in specialist centres. The Registry is a world-leading resource, the data from which is used to facilitate research, clinical trials, pharmacovigilance studies and quality improvement projects for the benefit of people with cystic fibrosis. You will be involved in the management and analysis of UK CF Registry data to support these work programmes.
We are looking for someone with a passion for working with healthcare data and the use of data to improve health outcomes. You will have experience in data management, analysis, and interpretation of healthcare data. With excellent communication skills, you will be able to communicate your work clearly and appropriately for a wide range of audiences. You will join a dynamic, collaborative team and work with colleagues and stakeholders both nationally and internationally. You will be passionate about supporting the Cystic Fibrosis Trust in its aim fighting for a life unlimited for everyone affected by cystic fibrosis.
You can find out more about what we do on our website.
The Cystic Fibrosis Trust welcomes applications from candidates from all backgrounds and particularly from people with Cystic Fibrosis, disabled people, and Black, Asian, and Minority Ethnic (BAME) and LGBTQI candidates.
Please note: if you decide to apply for this role, you will need to have the right to work in the UK before starting work for us and we will need to check this.
Closing date for completed application will be 07 November 2021
Interviews are expected to be held on w/c 15 November 2021
The client requests no contact from agencies or media sales.