Research Biostatistician

Research Biostatistician

Evotec

Verona, Italy

The ideal candidate will have a solid background in SAS programming and a strong understanding of CDISC standards. Familiarity with other programming languages is an added advantage.

Primary Responsibilities

• Programming support for both clinical and non-clinical studies to ensure that the data package adheres to CDISC standards (SDTM ADaM SEND).
• Develop, validate and standardized programming process and quality check using SAS/R/Python to analyze data and generate reports.
• Develop and review of randomization specifications and generation of randomization schedules.
• Review CRF and other study specific specifications and plans.
• Provide support and training to team members on best practices in programming and statistical analysis.
• Collaborate with multidisciplinary teams to define analysis specifications and ensure the accuracy of results.
• Participate in brainstorming sessions and innovation workshops to improve existing processes and implement new technologies.
• Meet deadlines and deliver high quality work.
• Regular report presentation in meetings and frequent communication with internal project team members and external clients references.

Required skills or attributes

• Bachelor or Master in Statistics, Computer Science or relevant field is desirable.
• Good understanding of pharmaceutical Research & Development processes and regulations.
• Demonstrated professional experience as SAS Programmer in pharmaceutical industry, CRO or Biotech/Biopharma.
• Strong capabilities and experience in using: SAS, R , Python.
• Networking, communication, facilitation skills.
• Experience with CDISC/SDTM, ADaM standards is preferred.
• Good data management skills and attention to detail is essential.
• Ability to meet strict deadlines and to work as part of a team.
• Motivation and analysis skills.
• Good verbal and written English

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