drjobs Clinical SAS Programmer

Clinical SAS Programmer

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1 Vacancy
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Job Location drjobs

Edison, NJ - USA

Monthly Salary drjobs

Not Disclosed

drjobs

Salary Not Disclosed

Vacancy

1 Vacancy

Job Description

Responsibilities:
  • Serve as the statistical programming lead on internal project teams and coordinate programming verification and documentation of statistical programs for use in creating analysis datasets tables listings and figures.
  • Facilitate advanced technical expertise in conjunction with internal and external team members to design implement validate and maintain project reporting applications that are supported by the department.
  • Assist in ensuring the optimum performance of group function. May recommend and implement techniques to improve productivity increase efficiencies cut costs take advantage of opportunities and maintain state-of-the-art practices.
  • Work independently to carry out assignments with little direct supervision.
  • Identify project priorities and project timeline goals and communicate priority related issues and timelines to programming teams.
  • Ensure the efficiency quality and integrity of data reporting and project activities executed.
  • Successfully represent the department and the company in sponsor meetings/presentations and maintain a positive working relationship with sponsors collaborating associates and vendor personnel.
  • Maintain awareness of project budgets and tasks and effectively communicate the status of such tasks to line management and the project manager as appropriate.
  • Perform other duties as required by the Department.
Requirements:
  • I have an undergraduate degree or higher in Biostatistics mathematics Computer Science or equivalent.
  • 3 years of Statistical Programming/Statistics experience or an equivalent combination of education and experience to successfully perform the key responsibilities of the job.
  • 3years of one or more statistical software packages (SAS preferred and/or R and/or Python) used to conduct statistical analyses.
  • 3 years working knowledge CDISC standards.
  • Previous experience in pharmaceutical research or CRO setting required.
  • Energized self-starter.
  • Excellent organizational skills.
  • Excellent communication skills verbal and written.
  • Exceptional attention to detail.
  • Flexible team player.
  • Proven ability to organize and effectively prioritize workload and deliverables.

Employment Type

Full Time

Company Industry

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