Instagram
youtube
Facebook

System Administration Support

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: System Administration Support

Location: India – Hyderabad (On Site)
Job ID: R-211343
Date Posted: March 28, 2025
Category: Clinical
Company: Amgen


Job Summary

Amgen is seeking a Manager – System Administration Support to manage Rave EDC user access, system upgrades, and cross-functional coordination related to EDC platforms (Classic Rave, Rave EDC, and others like Veeva). This role requires strong technical, organizational, and project coordination skills to ensure smooth operation and compliance within the Global Development Operations (GDO) Systems team.


Key Responsibilities

  • Oversee Rave EDC user access across studies and manage system upgrades.

  • Coordinate cross-functional activities related to Classic Rave and Rave EDC releases.

  • Collaborate with EDC vendors to translate business needs into technical solutions.

  • Support the evaluation and risk assessment of alternative EDC platforms (e.g., Veeva).

  • Manage documentation related to system access and upgrades, including M&A transitions (e.g., Horizon).

  • Organize and manage Rave FMT meetings and communications.

  • Ensure timely validation, testing, and documentation of system changes.

  • Act as liaison for stakeholders and IT regarding system enhancements and automation.


Basic Qualifications

  • Master’s degree + 4–6 years experience

  • OR Bachelor’s degree + 6–8 years experience

  • OR Diploma + 10–12 years experience


Required Skills

  • Strong technical and analytical skills; capable of managing multiple simultaneous projects.

  • Deep understanding of EDC systems and validation cycles.

  • Knowledge of GDO platforms, regulatory compliance, and process optimization.

  • Experience with Microsoft Office and collaboration tools (e.g., Teams, WebEx).


Good-to-Have Skills

  • Familiarity with pharmaceutical/clinical research terminology.

  • Experience in multinational environments and working with global teams.

  • Exposure to project management tools, AI/automation in EDC validation.

  • Understanding of data privacy and compliance.


Soft Skills

  • Exceptional communication (written and verbal)

  • High attention to detail and professionalism

  • Problem-solving, adaptability, and resilience


Why Amgen

  • Global biotech leader with over 40 years of innovation

  • Collaborative, inclusive, and science-driven culture

  • Competitive rewards and career development opportunities


How to Apply

Visit: careers.amgen.com