Real World Evidence Consultant
hace 6 meses
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)
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