SAS Programmer I

Visa Hunt; Brasil; Presencial; BRL 60 000 - 100 000; Tempo integral

Resumo da oferta

Visa Hunt is seeking a skilled Statistical Programmer to support global clinical trials. You will develop analysis data sets, write programs for ADS, Tables, Listings and Figures, and ensure validations are documented.

Collaborating with international statisticians, data managers and programmers, you will deliver data analyses and reporting, while maintaining high quality standards and clear communication across teams.

Qualificações

• University/Master's degree in applied science, mathematics, statistics or the like
• Knowledge of SAS software (SAS BASE/SAS STAT/SAS GRAPH) and experience of work in SAS system is desirable
• Good knowledge of programming logic, SQL and macro programming is preferred
• Proficient in English, spoken and written
• Experience within clinical trials and/or Biostatistics
• Good analytical skills
• Proficiency in standard MS Office applications
• Excellent communication and interpersonal skills

Responsabilidades

• Develop analysis data sets structure
• Develop program requirements and specifications
• Be involved in SAS programming of ADS and Tables, Listings and Figures
• Support SAS program validations
• Prepare and review program documentation
• Produce TFL
• Communicate with project teams and company departments with regard to statistical programming of clinical research projects

Conhecimentos

SAS programming

SQL

Macro programming

English skills

Analytical skills

MS Office

Formação académica

Master's degree in statistics

Bachelor's degree in applied sciences

Ferramentas

SAS

MS Excel

Descrição da oferta de emprego

You will contribute to statistical programming activities related to global clinical trials, work closely with international teams of statisticians, programmers and data managers, program data sets and summaries.

You will:

• Develop analysis data sets structure
• Develop program requirements and specifications
• Be involved in SAS programming of ADS and Tables, Listings and Figures
• Support SAS program validations
• Prepare and review program documentation
• Produce TFL
• Communicate with project teams and company departments with regard to statistical programming of clinical research projects

• University and Master's degree in applied science, mathematics, statistics or the like
• Knowledge of SAS software (SAS BASE/SAS STAT/SAS GRAPH) and experience of work in SAS system is desirable
• Good knowledge of programming logic, SQL and macro programming is preferred
• Proficient in English, spoken and written
• Experience within clinical trials and/or Biostatistics
• Good analytical skills
• Proficiency in standard MS Office applications
• Excellent communication and interpersonal skills

Our mission is to be the best CRO in the world as measured by our employees, clients, sites, and vendors. Our recruitment process is easy and straightforward, and we’ll be there with you every step of the way.

We are the company that cares - for our staff, for our clients, for our partners and for the quality of work we do. A dynamic, global company founded in 1995, we bring together more than 2,700 driven, dedicated and passionate individuals. We work on the frontline of medical science, changing lives, and bringing new medicines to those who need them.