Our open positions for your career

We are continuously looking for new talents to join our biostatistics and programming team.

If you want to work in a dynamic and expert team, which share the passion of statistics applied to clinical research,

please check the currently available positions and send us your CV at contact@signifience.com

Our positions are either based in France (Paris) or home based.

Senior Biostatisitician  /  Junior Biostatistician /  SAS programmer

Senior Biostatistician

Responsabilities

  • Responsible for providing statistical support to clinical studies or clinical data analytics projects.
  • Drafting, review and validation of study protocols including study design & sample size calculations.
  • Developement of statistical analysis plans including analysis dataset & TLG specifications.
  • Performing of statistical analyses required for the project.
  • Collaboration with clinical teams to assist them in interpreting results and preparing clinical study reports, including integrated summaries for submissions.

Requirements

  • MSc or PhD in statistics or applied mathematics with 5+ years of experience in Clinical Trials and/or Real Life Evidence studies.
  • Knowledge of medical/biological terminology and clinical trial designs in relevant therapeutic areas
  • Strong oral and written English skills, including technical writing.
  • Experience in SAS programming & knowledge of SAS procedures (knowledge in R is a plus)


Junior Biostatistician

Responsabilities

  • Participate in the developpement of study protocols and statistical analysis plans
  • Calculate the number of subjects required
  • Participate in the writing of statistical analysis and study reports
  • Collaboration with clinical teams to assist them in interpreting results and preparing clinical study reports

Requirements

  • MSc or PhD in statistics or applied mathematics
  • Very good knowledge in statistical tools (regressions, censored data, mixed models, Kaplan Meier curves…)
  • Knowledge of medical/clinical terminology and clinical trial designs in relevant therapeutic areas
  • Strong oral and written English skills, including technical writing
  • Knowledge in SAS programming & SAS procedures (R is a plus)

 

SAS Programmer

Responsabilities

  • Support SAS programming and validation
  • Develop Analysis Data Sets
  • Produce Tables, Listings and Figures
  • Develop program requirements and specifications
  • Program SAS Macros where required
  • Collaborate with biostatisticians and clinical research teams to specify the project requirements

Requirements

  • Degree in biostatistics or SAS programming
  • Strong knowledge and experience in SAS software (SAS BASE/STAT/GRAPH)
  • Good knowledge in CDISC standards
  • Good knowledge in SQL language
  • Experience within clinical trials environnement
  • Strong oral and written English skills, including technical writing

SIGNIFIENCE

PariSanté Campus

2 – 10 Rue d’Oradour-sur-Glane

75015 Paris

contact@signifience.com