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Lead Statistical Programmer II

2 months ago

Blue Bell, Pennsylvania, United States Pharmaceutical Research Associates, Inc. Full time

Company Overview:
Pharmaceutical Research Associates, Inc. is seeking a highly skilled Lead Statistical Programmer II to join our dynamic team.


Key Responsibilities:

  • Produce exceptional SAS programming outputs for all projects, ensuring adherence to timelines, quality benchmarks, and contractual obligations.
  • Oversee programming deliverables for designated studies, including resource allocation, progress tracking, and quality assurance of junior programmers' outputs.

Additional Duties:

  • Keep leadership updated on project progress regarding quality, timelines, and performance challenges.
  • Follow programming specifications and study-specific requirements, ensuring all necessary documentation is completed and filed appropriately.
  • Utilize SAS efficiently while adhering to established programming guidelines.
  • Generate listings and safety outputs (analysis datasets, tables, figures) with a high degree of quality and precision.
  • Validate listings and safety outputs according to departmental protocols.
  • Create efficacy outputs (analysis datasets, tables, figures) maintaining high standards of quality and accuracy.
  • Validate efficacy outputs in line with departmental procedures.
  • Develop complex programs (including project or departmental macros) with a focus on quality and accuracy.
  • Collaborate effectively with other functions within the organization as necessary throughout the project lifecycle.

Professional Development:
Continuously learn, share, and implement new techniques and technologies to enhance efficiency and apply industry-standard solutions (e.g., SDTM, ADaM).


Qualifications:
A Bachelor's degree in Computer Science, Statistics, Mathematics, or a related scientific field, accompanied by six (6) years of relevant experience; or a Master's degree in the same fields with three (3) years of experience.


Essential Skills:

  • Expertise in programming statistical analyses using appropriate software tools (e.g., SAS), including the creation of tabulation datasets.
  • Actively participate as a key member of the project team, collaborating with biostatisticians, data managers, and project managers.
  • Proficient in programming techniques such as macro language, advanced data manipulation, and statistical procedures.
  • Strong understanding of analysis data structure standards (ADaM) and, if applicable, tabulation data structure standards (SDTM).
  • Contribute to departmental initiatives and serve as a subject matter expert on relevant technical topics.
  • Exhibit leadership capabilities in coordinating clinical study programming activities and projects.
  • Conduct analyses and investigations to identify and define issues, anticipating potential challenges. Work independently with critical review at key stages.

Remote work options are available. Candidates must have the legal right to work in the U.S.