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Global Regulatory Writing – Senior Manager

Amgen
12-17 years
INR 35 LPA – 50 LPA
Hyderabad
1 June 18, 2026
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: Regulatory Affairs, Regulatory Writing, Regulatory Compliance, Global Submissions, eCTD, IND/NDA/BLA Submissions, ICH-GCP, Regulatory Strategy, Regulatory Intelligence, Labeling Strategy.

Global Regulatory Writing – Senior Manager

Location: Hyderabad, India
Employment Type: Full-Time
Work Mode: On-Site

Role Summary

The Senior Manager – Global Regulatory Writing is responsible for authoring, reviewing, and securing approval of scientific and regulatory submission documents in compliance with global regulatory standards. This role serves as a functional lead on cross-functional product teams, drives regulatory writing strategies for complex submissions, mentors junior writers, and contributes to departmental and organizational initiatives.


Group Purpose

To prepare high-quality scientific and regulatory submission documents that comply with global regulatory requirements and support successful product development and regulatory approvals worldwide.


Key Responsibilities

Regulatory Writing & Document Development

  • Author or oversee the preparation of regulatory submission documents, including:

    • Clinical Study Reports (CSRs)

    • Investigator Brochures (IBs)

    • Responses to Regulatory Questions

    • Clinical Protocols and Amendments

    • Informed Consent Forms (ICFs)

    • Table of All Studies (TOAS)

    • Clinical Overview Addenda

    • eCTD Module 2 Clinical Summary Documents

    • Briefing Documents

    • Pediatric Investigation Plans (PIPs)

    • Other regulatory and scientific documents

  • Ensure documents meet global regulatory standards and submission requirements.

  • Conduct formal document reviews and approvals in accordance with applicable SOPs and quality standards.

Regulatory Submission Leadership

  • Lead regulatory writing activities for complex submissions, including:

    • INDs (Investigational New Drug Applications)

    • NDAs (New Drug Applications)

    • BLAs (Biologics License Applications)

    • Supplemental Applications

  • Provide strategic writing expertise throughout the product development lifecycle.

  • Support preparation of high-quality regulatory submissions for global health authorities.

Cross-Functional Collaboration

  • Serve as Functional Area Lead on product teams, including:

    • Global Regulatory Teams

    • Evidence Generation Teams

    • Global Safety Teams

    • Label Working Groups

  • Provide regulatory writing input to Global Regulatory Plans and team objectives.

  • Collaborate with clinical, regulatory, safety, biostatistics, and medical affairs teams.

Leadership & Team Development

  • Oversee the work of contract and freelance medical writers.

  • Train, mentor, and guide junior regulatory writers.

  • Support talent development and knowledge-sharing initiatives.

  • Lead departmental and cross-functional improvement projects.

Project & Timeline Management

  • Develop and manage document timelines and deliverables.

  • Ensure projects are completed within scope, quality standards, and timelines.

  • Monitor project risks and proactively resolve issues impacting deliverables.

Continuous Improvement

  • Stay current with evolving regulatory requirements, industry guidance, and emerging technologies.

  • Contribute to process improvements and best practices within regulatory writing.


Required Knowledge & Skills

Technical & Scientific Expertise

  • Ability to independently analyze complex scientific data and interpret findings.

  • Advanced expertise in scientific and regulatory writing and editing.

  • Strong understanding of clinical drug development and regulatory submission processes.

  • Expertise in preparing documents supporting all phases of clinical development and regulatory submissions.

Leadership & Communication

  • Excellent written and verbal communication skills.

  • Strong leadership, collaboration, negotiation, and influencing abilities.

  • Ability to work effectively in cross-functional and global team environments.

  • Strong analytical and decision-making capabilities.

Project Management

  • Excellent time management and organizational skills.

  • Ability to manage multiple projects simultaneously.

  • Self-motivated with a strong focus on results and accountability.

Regulatory Knowledge

  • Strong understanding of:

    • ICH Guidelines

    • Good Clinical Practice (GCP)

    • Global Regulatory Submission Requirements

    • Regulatory Writing Standards

  • Ability to develop, interpret, and implement SOPs, guidance documents, and work instructions.

Technology Skills

  • Advanced proficiency in:

    • Microsoft Word

    • Microsoft PowerPoint

    • Microsoft Excel

    • Document Management Systems


Preferred Qualifications

  • Deep understanding of scientific and technical writing principles.

  • Advanced knowledge of document management systems.

  • Industry experience in pharmaceutical, biotechnology, or CRO environments.

  • Extensive experience supporting global regulatory submissions.