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Senior Consultant, Medical Writing Expert

2 months ago

London, Greater London, United Kingdom IQVIA Argentina Full time
About the Role

We are seeking an experienced Senior Consultant, Medical Writing to join our Evidence Synthesis practice at IQVIA Argentina. As a key member of our team, you will be responsible for leading day-to-day activities of multiple evidence synthesis projects, providing senior technical and statistical leadership, and driving the development of innovative methods and research outputs.

Key Responsibilities
  • Client Engagements
    • Lead evidence synthesis projects, including the development of statistical analysis protocols (SAP) and conduct of feasibility assessments, evidence synthesis by means of meta-analysis, indirect treatment comparison or network meta-analysis.
    • Provide senior technical and statistical leadership and effective ad hoc problem-solving support to the delivery of diverse evidence synthesis projects.
    • Edit, review, and develop scripts to ensure accurate and efficient implementation tailored to specific research problems.
    • Provide technical guidance, input and quality control for key deliverables (e.g., draft protocols, statistical analysis plans, reports, manuscripts).
    • Support project implementation including overall project management and client engagement.
  • Driving Development
    • Establish research credentials and further the wider IQVIA profile in evidence synthesis through the development of innovative methods and the dissemination of research outputs in peer-reviewed journals and scientific conferences.
    • Support the development of product offerings and internal process optimization as part of the Centre of Excellence for Indirect Treatment Comparisons.
  • Mentoring
    • Coaching and training for junior statisticians and project delivery teams.
Requirements
  • Essential Qualifications
    • Master's degree in (medical) statistics, biostatistics, mathematics, epidemiology, public health, health economics or a related discipline.
    • PhD in a subject related to health services research or statistics is desirable.
  • Essential Skills, Knowledge and Personal Behaviours
    • At least 5 years prior relevant experience working as a statistician in consultancy, CRO, pharmaceutical/biotech or academia (as post-graduate researcher).
    • Strong programming skills in R and good command of Stan or WinBUGS/OpenBUGS/JAGS (other statistical software and decision support packages desirable), ability to provide evidence of this applied in a business or academic setting.
    • Strong quantitative skills and experience with Bayesian statistics, generalized linear models, feasibility assessments, direct and indirect treatment comparisons, population-adjustment (MAIC, STC, ML-NMR), surrogate endpoint evaluation, structured expert elicitation, survival analyses.
    • Excellent scientific writing skills. prior coaching and training experience is desirable.
    • Good project management skills with proven time management and organizational skills.