Senior Clinical SAS Programmer

Katalyst CRO; Philadelphia (Philadelphia County); On-site; USD 69,000 - 124,600; Part time

Job summary

A clinical research organization is seeking a Senior Clinical SAS Programmer in Philadelphia. This role involves developing CDISC-compliant datasets and supporting statisticians in analyses. The ideal candidate should have strong SAS programming skills and experience in clinical trials. This position is offered as a contract with competitive compensation ranging from $69,000 to $124,600 annually.

Qualifications

• Minimum years of experience in developing software for clinical trials using the SAS system.
• Skilled in programming with SAS; knowledge of additional programming languages is a plus.
• Experience as a lead programmer for NDAs/BLAs.

Responsibilities

• Developing CDISC-compliant datasets and documentation.
• Creating software systems for displays of clinical study data.
• Assisting statisticians with analysis requests.

Skills

SAS programming

Statistics knowledge

Clinical trials experience

Job description

Senior Clinical SAS Programmer

Job at Katalyst CRO

Location: Philadelphia, PA. Salary: $69,000.00 - $124,600.00

Summary

As a Clinical SAS Programmer, you will be responsible for attending multi-disciplinary team meetings to represent the programming function. You will create or review and approve programming plans at study and project levels, providing input on key study-related documents produced by other functions.

Key Responsibilities

• Developing CDISC-compliant datasets and corresponding documentation for electronic submission to regulatory agencies.
• Creating or reviewing software systems to generate displays of clinical study data as tables, listings, and graphs for electronic submission to regulatory agencies.
• Assisting statisticians by suggesting algorithms to address client analysis requests.
• Developing software validation procedures and test plans.

Requirements

• Minimum years of experience in developing software for clinical trials using the SAS system.
• Skilled in programming with SAS. Knowledge of additional programming languages a plus.
• Good knowledge of statistics and drug development process.
• Experience as a lead programmer for NDAs/BLAs.
• Experience overseeing the work of internal contractors and external vendors (CROs).

Seniority Level

Mid-Senior level

Employment type

Contract

Job Function

Information Technology

Industry

Pharmaceutical Manufacturing