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Guideline Research Fellow

Partnership Jobs
Job LocationWembley Central
EducationNot Mentioned
SalaryCompetitive salary
IndustryNot Mentioned
Functional AreaNot Mentioned
Job TypePermanent, full-time

Job Description

Guideline Research Fellow British Association of Dermatologists Central London(Full time, 1-year contract in the first instance)£35,000This is an exciting opportunity to join the Clinical Standards Unit of the British Association of Dermatologists (BAD), which produces clinical guidelines for the association. Our guideline development process is certified by NICE Accreditation. The unit also manages the BADs patient information leaflets, clinical audits, and health informatics activities.Our adoption of the more rigorous GRADE methodology for guideline development since 2013 means that an additional member of staff is required to join this small but very busy team, and provide increased support to an anticipated five to six guideline development groups (GDGs).Report to: Director of Clinical StandardsJob SummaryThe Guideline Research Fellow (GRF) will provide systematic review and some information science support to GDGs. For further details please see the full job description below.Potential candidates should get in touch with Dr M. Firouz Mohd Mustapa by an email via the button below to request the person specification, then forward a CV and covering letter clearly addressing how your skills and experience match the job description and person specification.Closing date:14th December 2020.Provisional interview date:January 2021.No agencies.Responsible to the Director of Clinical Standards, Chief Executive Officer, chairpersons of the Therapy & Guidelines sub-committee and relevant GDGs.RESPONSIBILITIES

  • Managing the systematic review element of clinical guideline production:
  • background reading to aid understanding of the clinical areas
  • assisting in the development of searchable clinical questions, e.g. using the PICO method
  • preparation of systematic review protocols
  • evaluating shortlisted articles against inclusion/exclusion criteria
  • data extraction
  • critical appraisal of studies
  • RevMan data syntheses, meta-analyses, forest plots
  • assisting with any network meta-analysis, where applicable
  • preparation of GRADE evidence profiles
  • preparation of summary tables of included comparative and non-comparative studies, lists of excluded studies and PRISMA diagrams
  • presenting summarised evidence at meetings
  • summarising identified evidence in narrative format in the Linking Evidence To Recommendations (LETR) section
  • ensuring methodological rigour of guideline development; monitoring adherence to NICE Accreditation
  • documenting all review processes and maintaining clear audit trails to assist reproducibility
  • leading/assisting with the preparation of offshoot systematic review publications, where applicable
  • Providing information science support to BAD GDGs:
  • assisting the BAD Information Scientist with the development and refinement of literature search strategies, in consultation with lead/senior GDG member(s)
  • assisting the BAD Information Scientist with shortlisting of abstracts (2nd round selection) or arbitration of disagreements
  • drafting relevant sections of the guideline
  • collating draft sections for the manuscript and supporting information document, and formatting according to house style
  • editing and proofreading manuscripts and supporting information documents
  • performing EndNote citations and creating bibliographies for guideline manuscripts and supporting information document
    • Providing administrative support to the chairpersons of GDGs:
  • planning for and arranging GDG meetings, including the preparation of agendas and minutes
  • coordination of communications, feedbacks and any official responses
  • keeping to scheduled/agreed timelines for each stage of the guideline development
  • summitting the guideline for publication to the BJD
    • Assisting with the maintenance of relevant pages of the BAD website (training will be given):
  • clinical standards
  • clinical guidelines
    • Liaising with the BAD Journal Office and publishers Attending the BAD Annual Conference:
  • assistance with all aspects of conference registration and organisation
  • servicing relevant GDGs
  • attending presentations and reading posters of relevance to guideline projects
    • Any other ad-hoc work

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