Non-Clinical Statistician

Buscojobs; Veneto; In loco; EUR 40.000 - 60.000; Tempo pieno

Descrizione del lavoro

A leading company in pharmaceutical solutions is seeking a highly motivated Statistical Programmer. This role involves programming support, developing specifications, and collaborating with multidisciplinary teams to ensure data accuracy. The ideal candidate will have a background in SAS programming and experience in the pharmaceutical industry, with opportunities for continuous training and professional growth.

Servizi

Growth opportunities

Continuous training

Work-life balance

Competenze

• Experience as SAS Programmer in pharmaceutical industry or CRO.
• Familiarity with CDISC/SDTM, ADaM standards preferred.
• Good understanding of pharmaceutical R&D processes.

Mansioni

• Programming support for clinical and non-clinical studies adhering to CDISC standards.
• Develop and validate programming processes using SAS/R/Python.
• Provide training to team members on best practices.

Conoscenze

SAS

R

Python

Communication

Facilitation

Analytical Skills

Formazione

Bachelor or Master in Statistics

Computer Science

Descrizione del lavoro

We are a dynamic team focused on delivering innovative solutions in statistics and data analysis. To meet the increasing demand for data analysis and standardization activities—supporting both Business Lines contracts and direct Pharmacometrics contracts with clients—we are seeking a highly motivated individual to join our Pharmacometrics team as a Statistical Programmer. 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 standardize programming processes and quality checks using SAS/R/Python to analyze data and generate reports.
• Develop and review 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.

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, and 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 analytical skills.
• Good verbal and written English.

What We Offer:

• A stimulating, young, and dynamic work environment with opportunities for growth and professional development.
• The chance to work on innovative and diverse projects.
• Continuous training and support for acquiring new skills.
• We value flexibility and prioritize work-life balance, understanding that a healthy equilibrium enhances both personal well-being and professional performance.

ENG : In the frame of our Diversity policy, Evotec considers, with equal competences, all applications including people with disabilities.