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
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