Biostatistician for Clinical Trials and Observational Studies

hace 1 semana


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

We are seeking a highly skilled biostatistician to join our team at the European Foundation for the Study of Chronic Liver Failure (EF CLIF). This role will involve providing statistical expertise in the design of statistical analysis plans (SAPs) for research projects and clinical trials, referring to senior statistical experts when necessary.

About the Role

The successful candidate will manage their own projects within their working schedule and apply a range of statistical methods to solve complex problems as part of a multidisciplinary team. Key responsibilities include:

  • Demonstrating independence in 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
About Us

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

About the Team

The successful candidate will join a dynamic team of 4 members, including bioinformaticians, statisticians, data managers, and the CTIO. The team is based in the EF CLIF Headquarters in Barcelona, Spain, and serves as a resource for our members and collaborators in tertiary care university hospitals across the world.

Requirements

To be considered for this role, you should have:

  • Familiarity with academic research and large-scale observational studies as well as clinical trials
  • Experience with case report form (CRF) and/or database management
  • Bachelor's degree/Masters Degree/Ph.D. which includes statistics (preferably medical statistics) with >3 years practical experience in applying statistics in clinical trials
  • Experience with database management and statistical software programming (SAS and/or SPSS, R, etc.)
  • Knowledge in specific statistical methods/techniques (survival analysis, modeling, etc.)
  • Familiarity with scientific articles' reading and writing
  • Familiarity with information technologies and computational applications
Competences

The ideal candidate will have 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, as is the ability to work as part of an interdisciplinary team.

Salary and Benefits

This position comes with a competitive salary of €65,000 - €85,000 per year, depending on experience. In addition, we offer a comprehensive benefits package, including health insurance, pension scheme, and generous annual leave.



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