Senior Biostatistician

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.

Desirable

• 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)