Evidence Synthesis Associate Consultant
hace 1 día
Join our team as an Evidence Synthesis Associate Consultant supporting rigorous analyses and critical appraisals of published medical evidence across a wide range of diagnostic, prognostic, therapeutic, and other clinical interventions, as well as drafting reports. This professional will also provide technical expertise on evidence synthesis methods, including meta-analyses and network meta-analyses.
The essential functions you would be in charge of are:
- Serves as research assistant on complex projects, including developing research protocol, conducting qualitative and quantitative synthesis, preparing reports, and highlighting implications of findings for patients, payers, industry, and other stakeholders.
- Support the conduction of evidence summaries, systematic reviews, meta-analyses, and other analyses to answer high-impact clinical questions
- Critically evaluate the research methods and statistical findings of health outcome studies retrieved from the medical literature; and use established frameworks and tools to evaluate, grade and summarize the quality of the evidence.
- Disseminate the findings of evidence reviews through slide decks and written reports
- Draft clinical effectiveness section of HTA and other evidence synthesis reports
- Assist with generation of evidence-based recommendations and policies related to the use of new and existing medical technologies (e.g., procedures, equipment, devices, diagnostics, and selected pharmacologic agents) as well as clinical interventions for medical conditions affecting large populations.
To fulfill the previous functions, we are looking for professionals who:
- Have a graduate degree or equivalent professional experience in life sciences. Master's degree in clinical epidemiology required (preferably near completion or completed).
- 1-2 years of experience in conducting health assessments, academic systematic reviews of the medical literature, or similar work requiring critical evaluation of medical evidence.
- At least one year of experience in consulting for clients in the pharmaceutical industry.
- Experience working in statistical programs like Stata or R.
- Experience conducting meta-analysis and network meta-analysis is desirable but not mandatory
- Experience in the critical evaluation of evidence, including the ability to critique the research methods and statistical findings of published studies in order to rate the overall strength of evidence that underlies an analysis of comparative effectiveness.
IQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry. We believe in pushing the boundaries of human science and data science to make the biggest impact possible - to help our customers create a healthier world. Learn more at
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