Sign up with

Already have an account? Log in here

Need some help?
Talk to us at +91 7670800001

SAS Programmer I at PSI CRO

Milan, Lombardy, Italy -

Full Time

Start Date

Immediate

Expiry Date

20 May, 26

Salary

0.0

Posted On

19 Feb, 26

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

SAS, SAS BASE, SAS STAT, SAS GRAPH, Programming Logic, SQL, Macro Programming, English, Clinical Trials, Biostatistics, Analytical Skills, MS Office

Industry

Pharmaceutical Manufacturing

Description

Company 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 Please submit your CV in English. 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 Qualifications University and Master's degree in Statistics or Biostatistics Knowledge of SAS software (SAS BASE/SAS STAT/SAS GRAPH) and experience of work in SAS system 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 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.

Responsibilities

The role involves contributing to statistical programming activities for global clinical trials, collaborating with international teams of statisticians, programmers, and data managers to program data sets and summaries. Key tasks include developing analysis data set structures, programming ADS, Tables, Listings, and Figures, and supporting SAS program validations.