Clinical SAS Programmer

cGxPServe; Edison (NJ); On-site; USD 70,000 - 95,000; Full time

Job summary

A leading research services company is looking for a Clinical SAS Programmer to lead statistical programming efforts. The ideal candidate will have substantial experience with SAS, alongside strong organizational and communication skills, to ensure high-quality data reporting and effective collaboration with project teams. This full-time role in Edison, NJ, offers an attractive salary and the opportunity to make a significant impact in pharmaceutical research.

Qualifications

• 3 years of Statistical Programming or equivalent combination of education and experience.
• 3 years of experience with statistical software packages.
• Knowledge of CDISC standards is required.

Responsibilities

• Serve as statistical programming lead and coordinate documentation of statistical programs.
• Work independently with little supervision to ensure data quality and integrity.
• Report project statuses and communicate effectively with sponsors and management.

Skills

Statistical Programming

Attention to Detail

Communication Skills

Organizational Skills

Education

Undergraduate degree in Biostatistics, Mathematics, Computer Science or equivalent

Tools

SAS

R

Python

Job description

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• 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.
  
  

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.

Seniority level

• Seniority level

  Mid-Senior level

Employment type

• Employment type

  Full-time

Job function

• Job function

  Information Technology

• Industries

  Research Services

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