Senior Biostatistician

Clinical Research · Paris

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Are you looking for a job where you can make a difference and work in a non-profit? Would you like to be a part of an ambitious and international organisation on the cutting edge of science? Then this position might be right up your alley.

The EBMT is a non-profit medical and scientific organisation which hosts a unique patient registry providing a pool of data to perform studies and assess new trends. 


Our mission

Save and improve the lives of patients with blood-related disorders.

Your mission

Independently write statistical analysis plans, analyse data, and reports results. 

Responsibilities and Tasks

  • Work with investigators on study proposal/ protocol development and writing manuscripts.
  • Take the statistical lead in studies and projects related to collaborations on topics including statistical software, and evaluation of methods.
  • Develop tools for implementing new statistical methods using commercial and open source statistical software (SPSS, R).
  • Interaction with data management staff in design and quality checking of study databases.
  • Provide statistical support in the areas of study design and proposal development, perform complex calculations, analysis, planning, protocol/synopsis writing, questionnaires' elaboration (together with principal investigator and study coordinator), and statistical analysis programming.
  • Provide guidance to clinical investigators on design, analysis and interpretation of the results.
  • Serve as content expert, supervising other biostatisticians. May in addition serve as technical referent for them.
  • Write the results and statistical methods for abstract and publication in peer-reviewed journal.
  • Presentation of results in scientific congresses.


  • Fluent in English, excellent oral and written skills.
  • Master’s degree in biostatistics, statistics or related field.
  • Minimum 5 years´ experience working as a biostatistician.
  • Experience with survival analysis .
  • Experience working with observational research and longitudinal data.
  • Advanced knowledge and understanding of the principles, concepts, methods, and standards of statistical research.
  • Expert knowledge of scientific reporting and manuscript preparation requirements and standards.
  • Excellent skills in SPSS, R and/or other statistical software.
  • Excellent ability to work with data of varying levels of quality and validity.
  • Strong knowledge of data management principles and regulatory requirements for data processing.
  • Strong analytical thinking, problem-solving skills and ability to communicate technical information to both technical and non-technical audiences in a multicultural / multilingual environment.
  • Excellent ability to analyse, interpret, and draw conclusions from complex data.


  • PhD in biostatistics, statistics or related field.
  • Experience with clinical study conduct and applicable legislation and GCP
  • Excellent ability to apply a range of advanced statistical techniques in support of clinical studies.
  • Medical knowledge

What we offer

  • Be part of a non-profit society where you can make a difference
  • Work alongside a multicultural and diverse international team
  • First year with CDD contract. Possibility to have a CDI after 1 year commitment
  • Flexible schedule (starting from 8 to 10 am and finishing accordingly)
  • Full-time contract, 37.5 working hours per week
  • 25 working days of Annual leave + 15 days RTT
  • Salary range between 45.000-50.000€ gross per year, depending on previous experience

Additional benefits (once probation period is over)

  • Transport allowance (Forfait mensuel NAVIGO Toutes Zones)
  • After probation period, EBMT supports nursery costs with a monthly supplement
  • Some days work from home and some days from the office (minimum 2 days at the office), although during the training period you will be mostly at the office.


Location (Hybrid)