Statistical Programmer

Katalyst CRO; New York (NY); On-site; USD 100,000 - 200,000; Full time

Job summary

An innovative firm is seeking a Statistical Programmer to support clinical trials in the pharmaceutical industry. This role involves collaborating with Biostatisticians and Data Managers to develop SAS programs for data analysis and reporting. The ideal candidate will have a strong background in SAS programming, attention to detail, and excellent communication skills. Join a dynamic team where your contributions will directly impact clinical research and ensure compliance with regulatory standards. This is a fantastic opportunity to grow in a pivotal role within the healthcare sector.

Qualifications

• 5 years of clinical statistical programming experience in the pharmaceutical industry.
• Proficiency in SAS programming and knowledge of regulatory requirements.

Responsibilities

• Provide programming support for clinical trials in the pharmaceutical industry.
• Ensure accuracy and consistency of clinical data through quality checks.

Skills

SAS Programming

Clinical Data Analysis

Attention to Detail

Problem-Solving Skills

Communication Skills

Education

Bachelor's Degree in Statistics

Bachelor's Degree in Computer Science

Tools

CDISC Data Standards

Job description

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• The SAS/Statistical Programmer will be responsible for providing programming support for clinical trials conducted within the pharmaceutical industry.
• The successful candidate will work closely with the Biostatisticians, Data Managers, and Clinical Research teams to develop and implement programming solutions to support clinical data analysis and reporting.
• The SAS/Statistical Programmer will also be responsible for ensuring the accuracy and consistency of clinical data.
• Develop and validate SAS programs to support clinical trial data analysis and reporting.
• Create, maintain, and document SAS programming standards and procedures.
• Collaborate with Biostatisticians, Data Managers, and Clinical Research teams to ensure programming requirements are met.
• Perform data checks, quality control checks, and data review activities to ensure data accuracy and consistency.
• Prepare datasets for analysis, including merging and cleaning data from various sources.
• Prepare and review tables, listings, and figures for clinical study reports.
• Ensure compliance with regulatory requirements and guidelines.
• Keep up to date with new SAS programming methods and software, as well as regulatory guidance.
  
  

Responsibilities

• The SAS/Statistical Programmer will be responsible for providing programming support for clinical trials conducted within the pharmaceutical industry.
• The successful candidate will work closely with the Biostatisticians, Data Managers, and Clinical Research teams to develop and implement programming solutions to support clinical data analysis and reporting.
• The SAS/Statistical Programmer will also be responsible for ensuring the accuracy and consistency of clinical data.
• Develop and validate SAS programs to support clinical trial data analysis and reporting.
• Create, maintain, and document SAS programming standards and procedures.
• Collaborate with Biostatisticians, Data Managers, and Clinical Research teams to ensure programming requirements are met.
• Perform data checks, quality control checks, and data review activities to ensure data accuracy and consistency.
• Prepare datasets for analysis, including merging and cleaning data from various sources.
• Prepare and review tables, listings, and figures for clinical study reports.
• Ensure compliance with regulatory requirements and guidelines.
• Keep up to date with new SAS programming methods and software, as well as regulatory guidance.
  
  

Requirements:

• Bachelor's Degree in statistics, computer science, or a similar quantitative field.
• 5 years of clinical statistical programming experience within the pharmaceutical or related industry.
• Proficiency in SAS programming.
• Knowledge of CDISC data standards.
• Strong attention to detail and ability to work independently.
• Excellent problem-solving skills.
• Excellent verbal and written communication skills.
• Ability to work in a team environment and collaborate effectively with other stakeholders.
• Knowledge of regulatory requirements for clinical trials and drug development.

Seniority level

• Seniority level

  Associate

Employment type

• Employment type

  Contract

Job function

• Job function

  Information Technology

• Industries

  Pharmaceutical Manufacturing

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