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Manager, Csar – Custom Function Programming

9-13 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 – Custom Function Programming

Location: India – Hyderabad (On Site)
Job ID: R-211537
Date Posted: March 28, 2025
Category: Clinical
Company: Amgen


Job Summary

Amgen is hiring a Manager – Custom Function Programmer within the Clinical Systems and Analytical Reporting (CSAR) team. This role focuses on the design and programming of clinical study databases, including advanced custom function development in EDC platforms such as Rave or Veeva. It involves working collaboratively with cross-functional teams, driving high-quality data collection standards, and improving systems through innovation and leadership.


Key Responsibilities

  • Build and program clinical studies using EDC technologies.

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

  • Provide custom function programming and edit check development.

  • Collaborate with Clinical Study Teams and other departments to deliver technical support.

  • Ensure compliance with GCP, regulatory standards, and Amgen SOPs.

  • Support decision-making with data insights and programming expertise.

  • Recommend or implement new tools or enhancements for platform efficiency.

  • Support audits and regulatory inspections through documentation and technical readiness.

  • Develop, review, and maintain SOPs and process documentation.


Required Knowledge & Skills

  • Strong experience in:

    • Custom function programming

    • EDC systems (e.g., Rave, Veeva)

    • Clinical trial platforms and databases

    • GCP and regulatory compliance

    • Problem-solving and analytical thinking

  • Knowledge of:

    • Data management and quality risk analysis

    • Project planning and cross-functional collaboration

    • Clinical trials and drug development lifecycle

    • Programming languages relevant to EDC customization


Basic Qualifications

  • Bachelor’s degree (or equivalent) in life sciences, computer science, business, or related discipline.

  • Clinical research experience in biotech, pharma, or CROs.


Preferred Qualifications

  • Advanced degree in a related field.

  • 9–13 years of experience in data management/programming.

  • Experience with vendor oversight (e.g., CROs, labs, IRT vendors).

  • Proven experience with clinical systems development, project management, and global team collaboration.


Why Join Amgen

  • Competitive total rewards package

  • Supportive, science-driven, and inclusive culture

  • Career growth opportunities in a global biotech leader


How to Apply

Apply online at: careers.amgen.com