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Manager, Csar – Custom Function Programming

0-2 years
Not Disclosed
10 April 9, 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 – Custom Function Programming

Department: Clinical
Company: Amgen
Location: Hyderabad, India
Work Location Type: On Site
Date Posted: March 28, 2025
Application Deadline: Not specified
Job ID: R-211537 


Job Summary:

Amgen is seeking a Manager, CSAR – Custom Function Programming, a key role supporting electronic data capture (EDC) systems in clinical trials. The individual will act as a Study Designer and Edit Check Programmer, ensuring high-quality deliverables in compliance with Amgen standards. The position requires a blend of leadership, technical programming, and clinical systems expertise to support clinical study teams and drive innovation in data-driven decision-making.


Key Responsibilities:

  • Design and program studies within the clinical trial database following Amgen standards.

  • Collaborate with CSAR Operations and cross-functional stakeholders for consistent, efficient EDC system use.

  • Act as a technical point of contact for system deliverables across studies and programs.

  • Coordinate and provide programming support to clinical study teams.

  • Evaluate and implement system enhancements and emerging technologies.

  • Develop, review, and enforce policies, SOPs, and associated documentation.

  • Support audits and ensure compliance with regulatory standards.

  • Analyze data trends and provide insights as a data scientist.

  • Manage project timelines and maintain comprehensive documentation for operational activities.


Knowledge Requirements:

  • Good Clinical Practice (GCP)

  • Clinical data management processes

  • Clinical trial databases and applications

  • Custom function programming and edit check development

  • Understanding of:

    • Drug development and trial lifecycle

    • Programming languages (unspecified, likely SAS, SQL, etc.)

    • Systems development lifecycle

    • Project planning and management

    • Risk analysis and quality management

    • Regulatory submissions and inspection readiness


Basic Qualifications:

  • Bachelor’s degree or equivalent in life science, computer science, business administration, or related field

  • Experience in life sciences or medically related field

  • Clinical research experience from pharmaceutical, biotech, or CRO environment


Preferred Qualifications:

  • Advanced degree in life sciences, statistics, computer science, or related field

  • Broad experience in clinical data management/programming in pharma/biotech

  • Experience overseeing vendors (CROs, central labs, etc.)

  • Exposure to process improvement methodologies and project management

  • Experience with EDC systems (e.g., Medidata Rave, Veeva)


Soft Skills:

  • Leadership and influencing skills

  • Strategic thinking and innovation mindset

  • Strong problem-solving and analytical skills

  • Collaborative and cross-functional team leadership

  • Effective written and verbal communication


Equal Opportunity Statement:

Amgen is an Equal Opportunity Employer. All qualified applicants will receive consideration without regard to race, religion, gender, orientation, disability, or veteran status. Accommodations are available for individuals with disabilities.