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Statistical Programmer II
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Statistical Programm....
drjobs Statistical Programmer II العربية

Statistical Programmer II

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1 Vacancy
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Job Location

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Bengaluru - India

Monthly Salary

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Not Disclosed

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Salary Not Disclosed

Vacancy

1 Vacancy

Job Description

Req ID : 2679203

Principal Duties Responsibilities

  • Perform and implement under supervision the following for clinical studies: (i) the SAS programming testing and documentation of statistical programs for use in creating statistical tables figures listings and graphs and (ii) the programming of analysis datasets (derived datasets) and transfer filesfor internal and external clients and (iii) the programmingquality control checks for the source data and report the data issues.
  • Provide technical expertise in conjunction with internal and external clients.
  • Develop programming documentation including specifications as appropriate under supervision.
  • Estimate programming scope of work manage resource assignments communicate project status and negotiate/renegotiate project timelines for deliverables.
  • Support other programmers within the DMC Statistical Center staff.
  • Understand and follow standard operating procedures for the independent statistical center
  • Assist in Department and Company projects as they relate to Biostatistical Services.
  • Provide coverage within the team and other teams as needed.
  • Other duties as assigned.

Job Requirements

Education

Bachelors degree required Masters degree preferred in computer science mathematics statistics or related fields.

Experience

  • Minimum of 1 year of recent experience with Statistical Programming in SAS environment.
  • Experience in pharmaceutical or medical devices industry preferred.

Knowledge Skills Abilities

  • Must have working understanding and expertise in SAS Base SAS graph and SAS Macros.
  • Capable of implementing statistical procedures as per specifications provided by biostatistician.
  • Must have working knowledge of CDISC standards (SDTM and ADaM)
  • Basic understanding of clinical trial data and be able to work hands on in data manipulations analysis and reporting of analysis results.
  • Good understanding of ICH E6 ICH E3 ICH E8 ICH E9 and clinical research processes.
  • Ability to work on multiple projects plan organize and prioritize activities.
  • Ability to communicate effectively verbally and in writing in English.
  • Excellent interpersonal skills to work effectively with others and provide high levels of customer service.
  • Ability to follow instructions and work independently as required; plan organize schedule and complete work within competing deadlines and priorities.
  • Ability to adapt to changes in office technology equipment and/or processes.
  • Demonstrated consistency and dependability in attendance quantity and quality of work.

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Remote Work :

No

Employment Type

Full Time

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