Design Analyst

  • Full time
  • Prague
  • Posted 1 week ago


The Design Analyst defines data needs, conducts design analytics, and develops and delivers reports and structured outputs to support protocol assessments and trial design decision making. This an individual contributor role.

Job overview

Perform, manage and co-ordinate activities for assigned opportunities/ projects. Utilize multiple data sources to perform analysis, develop data storyboards, collaborate internally to formulate meaningful client insights and reports, and present to internal and potentially external stakeholders. Train and support new team members / junior staff. Make recommendations for process improvements and contributes to innovation.


  • Accountable to ensure IQVIA planning services are providing a competitive edge in winning new business.
  • Take independent responsibility by delivering accurate and robust protocol assessments, in support of opportunities including but not limited to requests for proposals, early engagements, re-bids and potentially awarded studies.
  • Support the development of materials related to protocol assessments, customer bid defense meetings or internal customers such as Therapeutic Strategy Leads, Medical Leads, Project Leads, or business development
  • Collaborate with key stakeholders and IQVIA project teams to resolve issues
  • Prepare for insights meetings by conducting research into therapeutic areas using databases, scientific literature, the internet and expert medical knowledge, and draft data storyboard and insights report.
  • Lead insights meetings with internal stakeholders including Medical Directors, Therapeutic Strategy Leads, Business Developers, Sales Staff and Program Directors. Present results of data gathering and analysis activities, collaborate to translate data and analytics into meaningful actionable insights and finalize client report.
  • Has the ability to work proficiently across multiple TAs.
  • Train and support new team members.
  • Proficient with insights tools, demonstrate an in depth understanding of system features and functions to know what features are best used to accomplish an accurate protocol assessment.
  • Develops, and may present, complete client deliverables within known/identified frameworks and methodologies.
  • Proactively develops a basic knowledge of consulting methodologies through the delivery of consulting engagements and participation in formal and informal learning opportunities.
  • Proactively develops and manages project timelines and day to day communication with stakeholders
  • Minimum required education and experience

  • Typically requires 3 – 5 years of relevant experience in clinical research. Equivalent combination of education, training and experience.
  • Requires intermediate level knowledge of principles, theories, and concepts of a job area, typically obtained through advanced education combined with experience.
  • Bachelor’s Degree Healthcare or Biological Science
  • Clinical and/or data analytics and/or consultative experience is/are preferred.
  • General knowledge and understanding of company clinical systems, procedures, and corporate standards.
  • Good knowledge of medical terminology, GCP, FDA regulations, and Drug Development process.
  • In-depth understanding of clinical research.
  • Excellent communication, organizational and interpersonal skills.
  • Fluid report writing in English
  • Strong computer literacy, including well-developed computer skills in applicable software.
  • Ability to work independently and effectively prioritize tasks.
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