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Manager, Csar - Sas Edit Check Programmer

6-8 years
Not Disclosed
10 May 1, 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: 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