Senior Biostatistician for Clinical Trials and Observational Studies

hace 4 semanas


Barcelona, Barcelona, España EUROPEAN FOUNDATION FOR THE STUDY OF CHRONIC LIVER FAILURE EF CLIF A tiempo completo

We are seeking a highly skilled Senior Biostatistician to join our team at the European Foundation for the Study of Chronic Liver Failure (EF CLIF). The successful candidate will provide statistical expertise in the design of statistical analysis plans (SAPs) for research projects and clinical trials, referring to senior statistical experts where necessary.

The ideal candidate will have a strong background in biostatistics, with experience in applying statistical methods to solve complex problems in a multidisciplinary team. Key responsibilities will include:

  • Providing statistical support for standard design and interpretation of study data
  • Analyzing internal and external information to facilitate informed decision making and develop decision criteria
  • Applying modeling and simulation to inform study design and assess robustness of results
  • Developing SAPs for study and/or project delivery
  • Producing data analyses, supporting graphics and tables for study reports and publications
  • Interpreting, summarizing and communicating results of studies

The Data Management Center at EF CLIF coordinates all activities related to the development of clinical platforms, data cleansing processes, and biological sample management. The team operates in accordance with the FAIR principles, making data findable, accessible, interoperable and reusable, and applies the highest standards in clinical research and in compliance with the General Data Protection Regulation (GDPR).

The successful candidate will join a dynamic team of bioinformaticians, statisticians, data managers, and the CTIO, and will be based in the EF CLIF Headquarters in Barcelona, Spain. The role will involve working closely with our members and collaborators in tertiary care university hospitals across the world, enabling access to relevant clinical and laboratory data, and specimens through a secure environment.

The ideal candidate will have a strong methodological technical and analytical skills, with wide experience in clinical study design, data management and application of statistical approaches to research, elaboration of study protocols and scientific publications. Excellent organizational, prioritization, and communication skills are also essential.

The successful candidate will have a good command of the English language and will be able to work as part of an interdisciplinary team.



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