As the Practice Guideline Development Lead this role is responsible for collaborating with ASRM Practice Committee and task force members of medical experts to update and develop evidence-based clinical practice guidelines and practice committee opinions that answer and address clinical questions in reproductive medicine.
Essential Responsibilities: • Responsible for administration and oversight of ASRM Practice Committee. • Implements a defined process for recruiting, vetting, and appointing volunteers for document task forces. • Supports document development panels and methodology teams to follow defined processes, procedures, and plans according to timelines. • Ensure that ASRM adheres to a systematic process for guideline development, following criteria recommended by the National Academy of Medicine. • Supports a defined process by which ASRM solicits, reviews, prioritizes, and approves topics for new document development. • Design and conduct systematic literature searches in PubMed and other databases. • Assist with building evidence tables, extracting data, and creating summaries of evidence and conclusion statements. • Document process and archive all required materials for guideline inclusion in a national database. • Integrate written sections drafted by multiple authors into a single document. Prepare manuscripts for publication. • Implements a defined process to support decision-making to revise or retire published ASRM documents. • Oversee the development and dissemination of derivative materials in collaboration with others as needed. • Serve, as needed, as an ASRM staff representative for international educational collaborative initiatives. • Serve as ASRM staff representative to the Council of Medical Specialty Society Clinical Practice Guidelines Development Group.