SAS Programmer I

Reposted 11 Hours Ago
Be an Early Applicant
Hiring Remotely in São Paulo, BRA
In-Office or Remote
Entry level
Pharmaceutical
The Role
Contribute to statistical programming for global clinical trials: develop analysis datasets, write program specs, produce Tables/Listings/Figures (TFLs), validate SAS programs, prepare documentation, and liaise with project teams.
Summary Generated by Built In
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 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

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. 

Skills Required

  • University and Master's degree in applied science, mathematics, statistics or similar
  • 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
  • Knowledge of SAS software (SAS BASE/SAS STAT/SAS GRAPH) and experience in SAS
  • Good knowledge of programming logic, SQL and macro programming
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The Company
HQ: Zug
1,939 Employees
Year Founded: 1995

What We Do

PSI is a leading full-service global Contract Research Organization whose key strength is predictable patient enrollment across multiple therapeutic areas. PSI is known in the industry as a CRO focused on ‘on-time project delivery’. This is achieved through investing substantial effort and MD resources into performing quality feasibility assessments that provide an accurate predictor of study timelines. PSI’s global reach allows us to run clinical trials across multiple continents, in 50+ countries around the world. PSI’s reputation is that of a 'no-nonsense'​ CRO focused on timely patient enrollment and project delivery. An exceptionally high repeat and referral business rates alongside low staff turnover are indicative of our commitment to be the best CRO in the world as measured by our clients and our employees. http://www.psi-cro.com

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