GreenLight Clinical (Thailand) Co., Ltd.

รหัสงาน: BK-162978 | สถานที่ทำงาน: กรุงเทพ, ประเทศไทย

GreenLight Clinical (Thailand) Co., Ltd.

รหัสงาน: BK-162978 | สถานที่ทำงาน: ปทุมวัน, กรุงเทพ, ประเทศไทย

SAS Programmer

Why you’re here

 

We need programmers to complete the pipeline from data management and electronic Data Capture (eDC) through to the final Clinical Study Report (CSR). The industry standard language is SAS, we are happy to train programmers familiar with other languages. You will produce Clinical Data Interchange Standards Consortium (CDISC) datasets including Study Data Tabulation Model (SDTM) and Analysis Data Model (ADaM). These intermediate datasets will be used to create output Tables, Listings and Figures (TLF).

 

What you’ll deliver

 

  • Programming specifications for the creation of SDTM, ADaM and TLF outputs.
  • SAS programs and macros to produce SDTM, ADaM and TLF outputs.
  • SAS programs including substantial data merging and transformation.
  • Specifications for statistical output Quality Control (QC) processes.
  • QC verification of statistical output.
  • Statistical review of Case Report Forms (CRFs), database, and related documentation.
  • Specifications for data transfer and Food and Drug Administration (FDA) submission packages.

 

 

 

 

 

 

How we’ll measure it

 

  • Conformance of output to specifications.
  • Inspection/audit findings against procedures.
  • Output delivered on time, with high quality standards and within budget.

 

What you’re responsible for

 

 

  • Develop and review SAS programs and output as required for the management of clinical trial data, the tabulation of data according to Sponsor or CDISC SDTM standards, preparation of patient data listings, coding reports, graphical output, and creation of derived datasets and statistical analysis of data as specified in the Statistical or Report Analysis Plans.
  • Creation of ADaM datasets with associated TLFs, including tables with substantial statistical content.
  • Represent statistical programming at internal project meetings.
  • Demonstrate good problem-solving skills, a proactive approach and a willingness to make decisions, seeking advice from senior Biostatistics staff to confirm decisions when necessary.
  • Additional duties as requested to support statistical programming activities and QC.

 

Qualifications

 

  • Undergraduate degree or its international equivalent in clinical science or health-related field, computing, mathematical or statistical subject. Postgraduate degree preferred.
  • Statistical knowledge is highly regarded.

 

Work experience

 

  • Demonstrated experience working as a programmer or data transformation specialist, preferably in the pharmaceutical industry or CRO, but applicants with experience in other industries will be considered.
  • If not familiar with SAS, demonstrated ability to learn a new programming language on the job or by self-directed study

 

Technical knowledge & skills or other requirements

 

  • Demonstrated skills using SAS
    • Base SAS, SAS/STAT, data step, PROC SQL,SAS Graph and SAS Macro Language.
    • SQL ability very highly regarded
    • If not familiar with SAS, then you will have shown that you can learn new programming languages or computational systems on the job as required
  • Knowledge of clinical trials or the pharmaceutical development process is a plus
  • High level of programming and problem solving ability.
  • High level of English fluency.

 

 


รายละเอียดงาน:

  • ประเภทการจ้าง:

    งานเต็มเวลา
  • ระดับการศึกษา (ขั้นต่ำ) :

    ปริญญาตรี
  • ประเภทงาน:

  • สถานที่ทำงาน:

    ปทุมวัน, กรุงเทพ, ประเทศไทย
  • เงินเดือน:

    สามารถต่อรองได้

GreenLight Clinical (Thailand) Co., Ltd.
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