SAS Programmer I

Psi CRO; São Paulo; On-site; BRL 90,000 - 150,000; Full time

Job summary

PSI CRO in Brazil (São Paulo) seeks a Statistical Programmer to contribute to global clinical trials. You will work with statisticians, programmers and data managers, program data sets and summaries, and support SAS validations and documentation. Strong English and analytical skills are required.

Responsibilities include developing analysis data structures, creating ADS, Tables, Listings and Figures, and communicating with project teams to ensure high-quality deliverables.

Qualifications

• 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 and MS Office proficiency.
• Excellent communication and interpersonal skills.

Responsibilities

• 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 regarding statistical programming of clinical research projects.

Skills

SAS programming

Programming logic

SQL

Macro programming

MS Office

Analytical skills

Communication skills

Interpersonal skills

Education

Master's degree in applied science/statistics

University degree in applied science/statistics

Tools

SAS Base/STAT/GRAPH

Job description

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.

Job Description

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

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
• Prepareand review program documentation
• Produce TFL
• Communicatewith project teams and company departments with regard to statistical programming of clinical research projects

Qualifications

• 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 inEnglish, spoken and written
• Experience within clinical trials and/or Biostatistics
• Good analytical skills
• Proficiency in standard MS Office applications
• Excellent communication and interpersonal skills

Additional Information

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.

By clicking the link above or any third-party link within this posting, you are leaving this site and going to a third-party website where the third-party website's terms and privacy policy apply