Research Fellow - FGM Sister Study

We are seeking to appoint an autonomous and talented qualitative researcher to undertake research as part of a National Institute for Health Research Health Technology Assessment funded study (16/78/04). The ‘FGM Sister Study' aims to explore and understand female genital mutilation/cutting (FGM/C) survivors', male partners', and healthcare professionals' preferences for the timing of deinfibulation and their views on how FMG/C-related NHS services can best be delivered. This qualitative research study involves two work packages. The first aims to qualitatively explore the timing preferences for deinfibulation and how NHS FGM/C services can be improved for type 3 FGM/C-survivors (WP1a), male partners (WP1b), and healthcare professionals (HCPs) (WP1c). The second aims to use established techniques to validate the qualitative findings, inform best practice and policy recommendations around the timing of deinfibulation and FGM/C care provision, and identify future actions. 

The post-holder will be based in the Institute of Applied Health Research at the University of Birmingham. The post offers an exciting opportunity to work within the world leading women's health research community at the University, as well, with a range of NHS, Charity and Third Sector Organisations. It is anticipated that the successful candidate will have relevant experience of undertaking high quality women's health research and of working with vulnerable women and their families. 

Person Specification

• First degree in area of specialism and normally, a higher degree relevant to research area or equivalent qualifications 
• Evidence of successful and timely completion of qualitative or mixed-methods research 
• Self-motivated, pro-active, and able to use initiative where appropriate 
• Knowledge and understanding of FGM/C research and related issues
• Ability to communicate complex information clearly both orally and in written form 
• Good knowledge and understanding of ethical and research governance in health related research 
• Experience of participant recruitment and taking informed consent 
• Experience of using qualitative data collection methods (e.g. interviews/focus groups) 
• Experience of working with vulnerable women and their families 
• Evidence of peer-reviewed publications 
• Computer literate; experience of qualitative (e.g. NVivo) software 
• Experience of working in multi-disciplinary research teams 
• High level analytical capability 
• Understanding of and ability to contribute to broader management/administration processes 
• Ability to assess resource requirements and use resources effectively