Instagram
youtube
Facebook

Senior Associate, Global Submission Management - International

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 – International

Location: India – Hyderabad (On Site)
Job ID: R-206643
Date Posted: April 24, 2025
Category: Regulatory
Company: Amgen


Job Summary

Amgen is seeking a Senior Associate to manage regulatory submissions across international markets (excluding US and Canada). This role focuses on the planning, coordination, and technical compliance of submission content for clinical trials and marketing applications. Candidates should have strong expertise in Veeva Vault RIM, eCTD, and international regulatory requirements.


Key Responsibilities

  • Lead/support the creation and delivery of clinical trial and marketing application submissions

  • Manage Global/Submission Content Plans within Veeva Vault RIM

  • Collaborate with internal teams and external partners to ensure timely regulatory submission and archival

  • Interpret and operationalize regulatory guidance and requirements

  • Ensure compliance with submission standards (eCTD, NeeS, etc.) and Amgen SOPs

  • Contribute to strategy for communicating with international regulatory authorities

  • Drive continuous improvement in submission processes and tools

  • Participate in system validations and software updates

  • Represent submission function in global workstreams and projects


Required Knowledge and Skills

  • Expertise in eCTD/NeeS submissions (originals, amendments, periodic reports, etc.)

  • Advanced user of Veeva Vault RIM for planning and dashboard reporting

  • Experience with regulatory submission tools, preferably Lorenz docuBridge Explorer

  • Working knowledge of global and emerging market submission standards

  • Strong technical and project management skills


Preferred Knowledge and Skills

  • Familiarity with EU, JAPAC, GCC, and ZA regulatory submission requirements

  • Experience collaborating across departments (Regulatory Strategy, Safety, Clinical, CMC, Labeling, etc.)

  • Experience in cross-functional submission planning and project execution


Education & Experience Requirements

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

  • OR Bachelor’s degree with 4–6 years

  • OR Associate’s degree with 6–8 years

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


Why Join Amgen

  • Global impact in regulatory science

  • Opportunity to manage high-value projects across diverse geographies

  • Culture of innovation and continuous learning


How to Apply

Visit: careers.amgen.com