Senior Biostatistician

Madrid o Barcelona / Híbrido / Abierto hasta el 29/12/2023

Description of the tasks / routine work:

  • Providing statistical support to clinical studies,
  • Participating in the development of study protocols, including participation in study design discussions and sample size calculations;
  • Producing randomisation schedules;
  • Reviewing CRFs and data review guidelines; developing statistical analysis plans (SAPs);
  • Performing statistical analyses;
  • Interpreting statistical results;
  • Strong communication skills;

What We’re Looking For:

  • Master’s degree in statistics or a related discipline. PhD strongly desired.
  • 3+ years supporting clinical trial or RWE study in the Pharmaceutical or Biotechnology industry. Experience working for a CRO strongly desired.
  • Experience in sample size calculation, protocol concept development, protocol development, SAP.
  • Knowledge and implementation of advanced statistical methods.
  • Good SAS programming skills.
  • Knowledge of R programming a plus.
  • Strong knowledge of ICH guidelines.
  • Understanding & implementation of CDISC requirement for regulatory submissions is a plus.
  • ADaM specifications generation and QC of datasets is a plus.
  • Team player; willingness to go the extra distance to get results, meet deadlines, etc.
  • Ability to be flexible when priorities change and deal with ambiguity

Language level

  • Higher English level


  • Contract: Permanent full-time position
  • Starting date: As soon as possible
  • Flexible work schedule


What We Offer


You will be part of Evidenze Group, with high international projection and opportunities to progress in Senior and Leadership positions within the company. Join a team of more than 10 biostatisticians.

We are waiting to hear from you.