Job Title: Manager, CSAR – SAS Edit Check Programmer
Location: India – Hyderabad (On Site)
Job ID: R-212017
Date Posted: April 4, 2025
Category: Research
Job Summary
Amgen is seeking a Manager, CSAR – SAS Edit Check Programmer to lead SAS-based edit check programming for clinical trials. This role involves creating, testing, and implementing complex SAS edit checks in accordance with industry and Amgen standards, contributing to data quality and operational efficiency across multiple studies.
Key Responsibilities
Create, test, and implement SAS edit checks based on study requirements
Support and troubleshoot edit checks to ensure data integrity
Collaborate with Clinical Data Management and other stakeholders to meet project deliverables
Act as a technical expert on clinical systems (e.g., Rave EDC, Veeva EDC)
Participate in system transformation and improvement initiatives
Develop and maintain SOPs, validation documentation, and audit responses
Drive decision-making through data insights and quality analytics
Lead programming efforts across a study portfolio
Required Knowledge and Skills
Expertise in SAS programming and clinical edit check logic
Understanding of clinical data management systems and GCP
Familiarity with clinical trials, data lifecycle, and regulatory requirements
Strong analytical, problem-solving, and performance management skills
Capable of working in a matrixed, global, cross-functional environment
Experience with project planning, risk analysis, and quality control
Basic Qualifications
Bachelor’s degree in life sciences, computer science, or related field with 6–8 years of experience
OR Master’s degree with 4–6 years of experience
Experience in clinical research at a biotech, pharmaceutical, or CRO company
Preferred Qualifications
Advanced degree in a relevant field
Experience with data management in pharmaceutical or biotech sectors
Vendor oversight experience (e.g., CROs, central labs, IRT)
Familiarity with systems development lifecycle and emerging clinical tech
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