Real World Evidence Consultant
hace 3 semanas
Join our Team as a Real World Evidence Consultant to provide high quality, on-time input to client projects in the life sciences field. Assignments range in complexity from basic analysis and problem solving to assisting in the development of more complex solutions.
The essential functions you would be in charge of are:
- Design and implement systematic reviews of the literature, directed reviews or rapid reviews, meta-analyses
- Lead the outcome research team, providing guidelines and technical policies
- Assists with the review and analysis of client requirements or problems and assists in the development of proposals and client solutions.
- Assists in the development of detailed documentation and specifications.
- Performs quantitative or qualitative analyses to assist in the identification of client issues and the development of client specific solutions.
- Assists in the design/structure and completion of presentations that are appropriate to the characteristics or needs of the clients.
- Develops, and may present, complete client deliverables within known/identified frameworks and methodologies.
- Proactively develops a basic knowledge of consulting methodologies and the life sciences market through the delivery of consulting engagements and participation in formal and informal learning opportunities.
- Engagement based responsibilities are assigned and managed by Senior Consultants, Engagement Managers or Principals.
To fulfill the previous functions, we are looking for professionals thathave the following qualifications:
- Bachelor's Degree in health areas, with a master's degree in clinical epidemiology.
- Work experience in health research. Minimum two years of experience in health consulting, Evidence synthesis or HEOR (mandatory).
- Extensive experience in performing HTAs according to national and international guidelines (IETS, NICE, WHO), specifically clinical effectiveness and safety profile (mandatory).
- In-depth knowledge of the methodology for conducting secondary evidence synthesis studies (systematic literature reviews, Overviews, scoping reviews, conventional meta-analysis, network meta-analysis) (mandatory).
- Experience in construction of research proposals, epidemiological study protocols, technical reports, executive summaries and socialization of results (mandatory).
- Management of Stata and R. The Management of Python is desirable.
- Experience in medical writing and verifiable scientific publications (articles published in indexed journals) (required).
- Experience in technical leadership of health research projects, specifically in evidence-based medicine (mandatory).
- English level B2/C1. Fluency to communicate with native speakers on a technical level (mandatory).
- Experience or training in areas related to health economics and real life studies (desirable).
- Management of Article 72 (INVIMA register related)
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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