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Role and Responsibilities:

  • Maintains responsibility for all assigned duties within a clinical study, acting as study lead for multiple or complex studies.
  • Supports the review and development of clinical programs, contributing to complex methods and analysis sections of protocols.
  • Provides review and oversight to statistical output created by other team members.

Qualifications:

  • Master’s degree (or Higher) in biostatistics, statistics, mathematics or related disciplines.
  • Minimum of 6 years of related experience working in a Contract Research Organization.
  • Proficiency in one or more statistical programming language (SAS and R preferred).

Additional Information:

  • The position is also available in any of our European locations.
  • We prioritize diversity, equity, and inclusion by creating an equal opportunities workplace.
  • We offer training and career development opportunities internally with strong emphasis on personal and professional growth.

Ergomed Group

Ergomed Group is a rapidly expanding full-service mid-sized CRO specialising in Oncology and Rare Disease. Since 1997, the company has grown organically with operations in Europe, North America and Asia, fostering a true international culture that values employee experience, well-being, and work-life balance.

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