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Manager, Csar - Sas Edit Check Programmer

9-13 years
₹35-45 LPA
10 May 23, 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
Work Type: On Site
Job ID: R-211021
Date Posted: May 21, 2025

Estimated Salary: ₹35-45 LPA (based on industry standards for SAS programming leadership roles in Hyderabad)


Job Description:

Amgen is seeking a Manager, CSAR - SAS Edit Check Programmer to join its Clinical System and Analytical Reporting (CSAR) team. Reporting to the Sr. Manager, the successful candidate will be primarily responsible for programming and implementing SAS-based edit checks for clinical data systems. This role includes project management, technical leadership, and operational execution within global cross-functional teams.


Key Responsibilities:

  • Develop and implement SAS-based edit checks following Amgen’s standards and best practices

  • Collaborate with CSAR operations and cross-functional teams to deliver high-quality outputs for electronic data capture (EDC) technologies

  • Ensure timely and quality deliverables across studies and portfolios

  • Provide SAS programming expertise for clinical trial platforms

  • Support clinical study teams with programming deliverables and timelines

  • Act as a technical point of contact for system deliverables

  • Perform complex SAS edit check programming and conduct functionality testing

  • Contribute to transformation projects through project management, stakeholder engagement, and change management

  • Assist in SOP and policy development and audit preparedness


Knowledge & Skills:

  • Proficient in SAS edit check programming

  • Knowledge of Good Clinical Practice (GCP) and clinical trial data management

  • Familiarity with Rave EDC, Veeva EDC, and related technologies

  • Strong analytical, problem-solving, and decision-making skills

  • Understanding of clinical database development, SDLC, and regulatory filings

  • Ability to collaborate with global cross-functional teams and manage vendor relationships

  • Experience in risk analysis and quality management


Basic Qualifications:

  • Bachelor’s degree in Life Sciences, Computer Science, Business Administration, or related field

  • 9–13 years of experience in SAS programming, clinical data management, or related field

  • Proven team and project management experience

  • Strong understanding of the biopharmaceutical clinical research landscape


Preferred Qualifications:

  • Advanced degree in Life Sciences, Computer Science, or a related discipline

  • Experience in pharmaceutical or biotech industries, preferably with CRO oversight

  • Exposure to process improvement methodologies

  • Familiarity with project planning and matrix team environments


Join Amgen’s mission to serve patients by bringing forward innovative clinical technologies and data solutions. Be part of a team that makes a real impact in global health.

Apply Now at careers.amgen.com