We are looking for a highly motivated Project Administrator to join our research team. The successful candidate will work alongside our research, statistical and database teams on the International Severe Asthma Registry (ISAR). ISAR is the largest global research database on severe asthma patients, with data being provided from over 25 countries. The successful candidate will have a high attention to detail, a proactive approach and strong organisational and time management skills. Experience of working directly with health research data (clinical trials and/or registries) would be an advantage.  This is a fantastic opportunity to gain experience within an internationally recognised research organisation involved in the development and delivery of large-scale observational studies and pragmatic randomised controlled trials, including quality improvement. The successful candidate will become an integral part of our wider international team of researchers, clinicians, statisticians, and database technologists. This role will be based at our Cambridge office. Please send your application to [email protected] Primary responsibilities: Develop and review documentation including agreements, information sheets, training materials, presentations, and other resources Manage and respond to project related email, liaising with both internal and external project stakeholders Provide extensive administrative support to the Project Team Assist in the preparation of scheduled reports for external and internal stakeholders Arrange project and staff meetings, ensuring timely dissemination of minutes and actions Responsible for complex diary management which requires interaction with senior personnel both internally and externally Opportunity to attend international congresses across Europe and the United States

Does supporting world class research and improving lives of patients excite you? Our dynamic and internationally recognised research company Optimum Patient Care (OPC) is looking for a highly motivated Service Coordinator to join our Delivery Team normally based in Oakington, Cambridge. Please send your application to [email protected] Primary Responsibilities Facilitate the recruitment of General Practices into the OPC Quality Improvement programme and, where applicable, support practices’ enrolment onto other research studies Where required, support General Practices with patient recruitment in accordance with NHS information governance and UK Data Protection legislation. Update and maintain project delivery records, and produce monthly reports and other documentation. Support with data extractions for Quality Improvement programme and research projects Support with the delivery of OPC services as directed Managing company correspondence including phone enquiries. Represent the organisation at meetings, exhibitions, conference, education workshops and healthcare shows. Work as part of the OPC service team to maximise communication and build strong working relationships with practices

The successful candidate will work with a small team of experts to deliver a large pragmatic cluster randomised trial that incorporates quality improvement within UK primary care. Information about the study may be found here: https://opri.org.uk/magnify/ The successful candidate will have experience working in health research, have a high attention to detail and strong time management skills. This is a fantastic opportunity to gain experience within an internationally recognised research organisation involved in the development and delivery of large-scale observational studies and pragmatic randomised controlled trials, including quality improvement. The successful candidate will become an integral part of our wider international team of researchers, clinicians, statisticians, and database technologists. This role will be based at our Cambridge office. Please send your application to [email protected] Primary responsibilities: Develop and review project documentation including trial agreements, protocols, practice and patient information sheets, training materials, presentations, and other resources Recruit and coordinate GP sites ensuring professional relationships and regular communication with all participating sites Contribute to the development, review and implementation of patient and clinician resources including questionnaires, clinical decision support, feedback and promotional material. Code and verify data in accordance with specified research protocol and coding procedures, and enter data into a computer database and/or spreadsheet application for subsequent analysis. Create presentation slides and posters to help researchers recruit new GP practices. Occasional travel to GP sites to collect and record data as appropriate to the specific objectives of the study. Manage and respond to project related email, liaise with project stakeholders, and ensure timely dissemination of minutes and actions.