HEVA Analytics Evidence Synthesis Lead
Location: Chilly Mazarin; Barcelona
55% Remote working and 5% of travel expected
Job type: Permanent, Full time
ABOUT THE JOB Our Team
It plays a critical position with high responsibility as it ensures quality and accuracy of evidence generated from literature reviews intended for late-stage products in development (but not limited).
This evidence provides inputs to relative efficacy (comparative efficacy), economic model and Core Value Dossier (CVD) projects.
The CVD is shared with affiliates to prepare local submission dossiers.
The literature technical study reports are also shared with health authorities.
Main responsibilities
Under the supervision of the HEVA Analytics Team Head, the Evidence Synthesis Lead will participate in multiple scientific activities, listed here below:
In collaboration with relevant stakeholders:For Burden of Illness (BoI) projects: Designs and supervises focused / targeted BOI literature reviews.For Relative Efficacy Assessment projects (REA): Designs and supervises, in line with recognized guidelines (Cochrane, NICE, York University) systematic literature reviews (SLRs).Designs and supervises feasibility studies for indirect treatment comparisons (ITcs).Supports development of REA through ITCs based on efficacy & safety SLRs findings.Develops and supervises the corresponding of CVD based on BOI and REA projects' findings.Transversal activities:Give advice on, and supervise vendors for BOI, efficacy & safety or Health Technology Assessment (HTA) reviews.Keep abreast of new developments in Evidence Based Medicine (EBM) & HTA and ensure new research standards are followed and applied.Collaborate transversally with other functional groups within the Global Market Access department and other internal and external stakeholders.Authority to represent HEOR evidence synthesis in meetings where concerned expertise is needed.Provides information/education to internal stakeholders about the need, the methods and good uses of EBM and HTA methodology.Ensure that milestones and timelines are on track for simultaneously operating projects.ABOUT YOU Experience:
At least 5 years of relevant work experience, preferably as part of a team performing literature reviews and REA in pharmaceutical industry, CRO or academic experience in these fields.
All therapeutic areas are concerned.
Soft skills:
Flexibility and adaptability to internal and external changes.
Excellent organizational as well as written and oral communication skills.
Scientific rigor, autonomy, and sense of initiative.
Strong skills in analysis and synthesis of scientific information.
Technical skills:
Knowledge of the state-of-the-art in EBM and HTA research.
Excellent understanding of literature research principles, objectives pursued, and methods.
Extensive knowledge of literature review projects such as BOI, REA, or searches for published economic assessments (cost of illness, cost-effectiveness, and health state utility values) is required.
Full knowledge of platforms such as PubMed, Embase, or Ovid.
Knowledge of Health Technology Assessment databases HTA (i.E.
Prismaccess) is a plus.
Education:
Medical training (physician, pharmacist, or biologist) with MSc level on public health or epidemiology.
Languages:
English fluent both written and oral, French both written and oral is a plus.
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