RWE Technical Writer III

  • Contract
  • Remote

SimulStat

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Remote, 12-month contract, with potential to extend

The RWE Technical Writer III will ideally be someone who has a clinical research or epi background with immersion into developing protocols/reports and study analytics. While the key need is a scientific writer, it is nice to have someone understand analytics and its context for research protocols (candidates don’t necessarily need to be in a current analytics role).

Responsibilities:

  • The successful candidate will support Real-World Evidence (RWE) operations and communications and have an excellent understanding of fit-for-purpose analytic methods to employ across an array of RWE applications.
  • Implement and refine templates and processes for RWE generation.
  • Have an active role in communicating RWE purposes, processes, and methods across the organization.
  • Participate in planning and preparation of RWE studies, feasibility analyses and interpretation of data, abstracts, and study reports.
  • We anticipate this individual will be an active contributor to the development of research which ultimately helps to bring essential therapies to patients.
  • Ability to help RWE Leads with developing protocols is a requirement for this position.

Education / Experience / Skills:

  • Master’s degree (Epi, MPH, or Health Services) with 2+ years of experience in Epidemiology or RWE or PhD in related field
  • Protocol technical writing experience
  • Excellent knowledge of epidemiologic measures and pharmacoepidemiology methods
  • Excellent communicator
  • Ability to write processes & templates for research and document formatting

Nice to Have Skills / Experience:

  • Grant writing experience a plus
  • Experience analyzing and interpreting claims or EMR data
  • Technical education or curriculum development experience

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