SAS Programmer I
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Job Location:
Monthly Salary:
Posted on:
8 hours ago
Vacancies:
1 Vacancy
Job Summary
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 Masters 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 well be there with you every step of the way.
Remote Work :
Yes
Employment Type :
Full-time
Key Skills
- Databases
- SQL
- FDA Regulations
- R
- Relational Databases
- Data Management
- Data Structures
- Clinical Trials
- Statistical Software
- CDISC Standards
- SAS
- Oracle
About Company
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 effo ... View more
