Statistical Analyst III

Katalyst CRO; Illinois; On-site; USD 80,000 - 100,000; Full time

Job summary

A leading clinical research organization is seeking a Statistical Analyst III in Illinois. The ideal candidate will have expertise in SAS programming and substantial experience in the pharmaceutical industry. Responsibilities include data analysis, programming, and ensuring compliance with regulatory standards. This role requires strong communication skills and the ability to work independently to solve complex problems.

Qualifications

• 5 to 7 years of SAS programming experience in Pharmaceutical or related industry.
• Strong working experience in ADaM datasets creation and validation.
• Good CDSIC knowledge.

Responsibilities

• Create and validate ADaM, TLFs for CSR, ISS, and Client following standards.
• Review SAS programs for accuracy and resolve issues.
• Ensure consistency across studies within a project.

Skills

SAS programming

Statistical analysis

Clinical trials

Communication skills

Education

MS in Statistics, Computer Science, or a related field

BS in Statistics, Computer Science, or a related field

Tools

SAS

Job description

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Overview

Join to apply for the Statistical Analyst III role at Katalyst CRO

Responsibilities

• Demonstrated practical understanding of SAS programming concepts and techniques appropriate to the pharmaceutical industry.
• Demonstrated satisfactory ability to apply SAS programming knowledge and work independently to solve problems related to non-routine situations.
• Responsible for the creation and validation of ADaM, TLFs for CSR, ISS, and Client following SOPs, department, and project standards.
• Responsible for the accuracy of SAS programs by reviewing output, reviewing code, reviewing log files and resolving Pinnacle 21 checks.
• Responsible for the creation and accuracy of derivations as defined in the protocol and statistical analysis plan.
• Demonstrated satisfactory ability to interpret statistical analysis plans to develop analysis data set specifications.
• Ensure consistency across studies within a project.
• Responsible for the creation of data definition documents, TOCs, and support submission related activities.
• Learn and maintain expertise in the use of the utilities and macros developed for Statistical Programmers.
• Develop new macros and utilities.
• Provide accurate and timely responses to requests from clients with a sense of urgency.
• Be compliant with training requirements.

Qualifications

• MS in Statistics, Computer Science, or a related field with 5 to 7 years of SAS programming experience in Pharmaceutical or related industry OR
• BS in Statistics, Computer Science, or a related field with 5 to 7 years of SAS programming experience in Pharmaceutical or related industry.
• Strong experience with clinical trials, including familiarity with expectations of regulatory agencies,
• Strong working experience/skill in ADaM datasets creation/validation.
• Strong technical and communication skills, both oral and written.
• Competent in SAS programming, macro, and utilities development.
• Good CDSIC knowledge

Job function

• Research, Analyst, and Information Technology