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Associate, Regulatory Writing

1-2 years
Not Disclosed
10 April 11, 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: Associate, Regulatory Writing
Job ID: R-210834
Location: India – Hyderabad
Work Location Type: On Site
Department: Regulatory
Company: Amgen
Date Posted: April 3, 2025


Roles and Responsibilities:

  • Perform document-level Quality Control (QC) to ensure submission readiness, including:

    • Verifying abbreviations, data accuracy, references, and content alignment (text vs. tables/figures).

  • Apply Amgen formatting guidelines to create professional regulatory documents.

  • Ensure consistency in layout, fonts, margins, styles, and use of headers, tables, footnotes, etc.

  • Coordinate document collection from cross-functional teams.

  • Ensure documents are publishing-ready.

  • Participate in team collaboration and input gathering for noncomplex documents.

  • Support cross-functional document review processes.

  • Track project timelines and organize meetings with team members.

  • Learn and use Amgen’s authoring tools and platforms.

  • Attend cross-functional meetings for knowledge sharing and task updates.

  • Document types handled include:

    • Clinical Study Reports

    • Observational Research Study Reports

    • Plain Language Summaries

    • Investigator’s Brochures

    • Local Risk Management Plans

    • Noncomplex Protocols/Amendments

    • Plain Language Protocol Summaries

    • Informed Consent Forms

  • Follow SOPs, templates, writing guides, and internal policies.

  • Maintain product-specific reference libraries across therapeutic areas.


Basic Qualifications:

  • Bachelor’s degree in a science-related discipline from an accredited institution.


Preferred Qualifications:

  • 1–2 years of experience in regulatory or clinical document formatting and QC in pharma/biotech.

  • Basic scientific/medical knowledge and exposure to communication principles.

  • Familiarity with statistics and medical writing norms.

  • Strong oral and written communication skills.

  • Ability to build positive relationships across teams.

  • Strong attention to detail and accuracy.

  • Good organizational and multitasking abilities.

  • Experience with document management systems and tools such as Microsoft Office and SharePoint.