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Manager - International Regulatory Lead

10-12 years
Not Disclosed
10 April 9, 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

Position Title:

Manager – International Regulatory Lead (IRL)


Location:

India – Hyderabad (On Site)


Job ID:

R-211202


Date Posted:

April 04, 2025


Category:

Regulatory


Department:

International Regulatory Team, Global Regulatory Affairs


Role GCF:

5A


About Amgen:

Amgen is a pioneer in biotechnology, dedicated to discovering, developing, manufacturing, and delivering innovative medicines to improve lives. With a history of over 40 years, Amgen is driven by science, technology, and the power of human genetic data to tackle the toughest diseases.


Role Overview:

The International Regulatory Lead (IRL) Manager provides regulatory leadership and expertise across international markets for one or more Amgen products. This position collaborates with global and local regulatory teams to:

  • Optimize product development and approval pathways.

  • Develop and execute international regulatory strategies.

  • Support product registration and lifecycle management.


Key Responsibilities:

  • Advise global teams on international regulatory implications for clinical development and marketing applications.

  • Offer direction on regulatory pathways (e.g., FIH studies, Orphan Drug, expedited designations, reliance mechanisms).

  • Plan regulatory submissions for clinical trials and marketing authorizations.

  • Contribute to international regulatory strategy documentation and communicate key outcomes/risks.

  • Maintain and author documentation for clinical trials and/or marketing applications (excluding CMC).

  • Lead label submission strategy and negotiation, manage label deviation outcomes.

  • Support local teams with health authority queries using knowledge management systems.

  • Represent international regulatory in GRT and other global teams.

  • Maintain ongoing communication with global/local teams on product strategy.

  • Monitor evolving regulations and policies affecting Amgen products.

  • Conduct regulatory research and precedent studies to guide submissions.


Basic Qualifications (One of the Following):

  • Doctorate degree, OR

  • Master’s degree + 10+ years of relevant regional regulatory experience, OR

  • Bachelor’s degree + 12+ years of relevant regional regulatory experience


Functional Skills – Must-Have:

  • Strong knowledge of international regulatory environments (clinical trial apps, marketing authorization, labelling, etc.).

  • Comprehensive understanding of regulatory principles and cross-functional impacts.

  • Awareness of international regulatory challenges and processes.


Functional Skills – Good-to-Have:

  • Conflict resolution and problem-solving abilities.

  • Cultural awareness for working across borders.


Soft Skills:

  • Excellent oral and written communication.

  • Scientific and clinical literacy.

  • Effective collaboration with global/virtual teams.

  • Initiative, motivation, and self-direction.

  • Strong organizational and prioritization abilities.

  • Team-focused with strong negotiation and influencing capabilities.


Equal Opportunity Statement:

Amgen is an Equal Opportunity employer. All qualified applicants will receive consideration without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran status, or disability. Reasonable accommodations will be provided as needed throughout the hiring process.