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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-206629
Date Posted: April 11, 2025
Category: Regulatory
Company: Amgen


Job Summary

Amgen is seeking a Senior Associate, Global Submission Management – International to ensure the smooth flow of regulatory submissions across global markets. The role will lead and support the creation, planning, and delivery of regulatory submission components, leveraging technical expertise to ensure compliance with global regulatory requirements. This position will require a strong background in international submission management and regulatory submissions.


Key Responsibilities

  • Lead and support various Clinical Trial and Marketing Application type submissions

  • Manage the creation, maintenance, and management of Global/Submission Content Plans

  • Serve as the point of contact between internal and external stakeholders for regulatory submissions

  • Ensure smooth delivery and archiving of regulatory documents in Veeva Vault RIM

  • Stay current on internal and external regulatory guidance, translating requirements into operational tasks

  • Represent departmental expertise in global/regional workstreams and regulatory projects

  • Contribute to the development of strategies for communicating with global health authorities

  • Lead and manage process development and improvement initiatives

  • Participate in information system updates and ongoing system validations


Required Skills and Experience

  • Master’s degree and 3-4 years or Bachelor’s degree and 4-6 years of directly related experience in regulatory submission management

  • Experience with eCTD format, NeeS, and paper submissions

  • Advanced knowledge of Veeva Vault RIM and the management of submission content plans, reports, and dashboards

  • Strong project management skills and experience working across multiple disciplines (e.g., Clinical, Safety, CMC, Regulatory Strategy)

  • Practical experience with submission requirements for EU, JAPAC, GCC, and ZA regions


Preferred Skills

  • Advanced knowledge of eCTD specifications and software (e.g., Lorenz docuBridge Explorer)

  • Expertise in global Clinical Trial and Marketing Applications regulations and guidance

  • Strong team leadership and coordination skills

  • Experience with system validation and information system updates


Why Join Amgen

  • Be part of a collaborative and innovative environment dedicated to serving patients

  • Competitive benefits and career growth opportunities

  • Work on impactful global regulatory projects


How to Apply

Visit: careers.amgen.com