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Senior Associate, Global Submission Management - Americas

4-6 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: Senior Associate, Global Submission Management – Americas

Location: India – Hyderabad (On Site)
Job ID: R-206638
Date Posted: April 7, 2025
Category: Safety
Company: Amgen


Job Summary

Amgen is seeking a Senior Associate to manage and coordinate regulatory submissions for the Americas (US, Canada, South America). This role ensures regulatory compliance, leads submission planning and dossier preparation, manages communications across internal and external teams, and maintains systems such as Veeva Vault RIM and eCTD tools. The role requires strong regulatory operations experience, project management skills, and technical proficiency in submission platforms and global regulations.


Key Responsibilities

  • Lead/support Clinical Trial and Marketing Application submissions and content plans

  • Coordinate cross-functional teams and external partners for timely submissions

  • Ensure compliance with global and local regulatory submission formats (eCTD, NeeS, paper)

  • Oversee submission archiving using Veeva Vault RIM

  • Contribute to strategy for global health authority communications

  • Lead or support process improvements and system validation projects

  • Monitor evolving regulatory guidance and translate into operations

  • Participate in updates and validations of regulatory information systems


Required Knowledge & Skills

  • Advanced knowledge of eCTD, NeeS, and paper submission formats

  • Expertise in Veeva Vault RIM: content plans, dashboards, maintenance

  • Experience with regulatory publishing tools (e.g., Lorenz docuBridge)

  • Familiarity with submission requirements for global markets

  • Ability to manage submission lifecycles and regulatory timelines

  • Strong project leadership and cross-functional collaboration skills


Preferred Qualifications

  • Practical submission experience for US, Canada, and South America

  • Advanced understanding of global regulatory frameworks

  • Knowledge of Clinical Trial and Marketing Application regulations

  • Strong communication and innovation mindset


Education Requirements

  • Master’s degree with 3–4 years of experience

  • Bachelor’s degree with 4–6 years of experience

  • Associate’s degree with 6–8 years of experience

  • High school diploma / GED with 8+ years of experience


Why Join Amgen

  • Impact global health through regulatory excellence

  • Work with cutting-edge tools and collaborative global teams

  • Benefit from comprehensive rewards and professional growth opportunities


How to Apply

Visit: careers.amgen.com