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Principal Sas Programmer

1-3 years
Not Disclosed
10 June 24, 2025
Job Description
Job Type: Full Time Education: B.Sc./M.Sc/B.Pharm/M.Pharm/Life Science Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

 

Job Title:

Principal SAS Programmer – Clinical Research


Job Summary:

We are hiring a Principal SAS Programmer to lead and manage clinical programming deliverables for global pharmaceutical and clinical research projects. The role involves guiding programming teams, ensuring adherence to CDISC, SDTM, and ADaM standards, and developing high-quality statistical datasets for efficacy and safety analysis. This position offers a chance to influence project success by applying advanced SAS programming knowledge while fostering client relationships and cross-functional collaboration.


Key Responsibilities:

  • Lead complex programming projects or manage at least two moderate complexity studies.

  • Oversee programming teams ensuring deliverables meet project objectives, timelines, and quality standards.

  • Develop and validate Safety and Efficacy Analysis Datasets according to CDISC, SDTM, ADaM, and client-specific standards.

  • Create and finalize programming specifications, macros, and mock-ups.

  • Troubleshoot and resolve programming issues efficiently.

  • Communicate proactively with biostatistics, programming, management, and sponsor teams.

  • Manage workload to ensure timely and effective project delivery.

  • Participate in process improvements, training sessions, and audit meetings with sponsors.

  • Maintain and improve client relationships through excellent project management and communication.


Required Skills & Qualifications:

  • Expertise in SAS programming for clinical research.

  • Strong understanding of CDISC standards including SDTM and ADaM datasets.

  • Proven people management and team leadership skills.

  • Excellent problem-solving, organizational, verbal, and written communication skills.

  • Ability to handle complex clinical data programming tasks.

  • Experience in developing, debugging, and maintaining standard macros and programs.


Perks & Benefits:

  • Competitive salary package (Not Specified)

  • Opportunity to work on global clinical trials

  • Professional growth with industry leaders in clinical research

  • Exposure to CDISC and regulatory-compliant data standards

  • Collaborative and supportive work culture


Company Description:

A globally recognized pharmaceutical services organization specializing in clinical research, data management, and statistical programming. The company focuses on delivering high-quality solutions for pharmaceutical and biotech industries worldwide.


Work Mode:

Remote / Hybrid / On-site (Location Not Specified)


Call to Action:

Ready to lead clinical programming projects with global impact? Apply now to join our expert SAS programming team and advance your career in clinical research!