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Global Regulatory Writing – Senior Manager

Amgen
10+ years
INR 35 LPA – 55 LPA
Hyderabad
1 June 29, 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

Company: Amgen
Location: Hyderabad, India
Department: Global Regulatory Writing
Job Type: Full-Time
Work Mode: On-Site

JOB OVERVIEW

The Global Regulatory Writing – Senior Manager is responsible for leading the preparation, review, and approval of complex scientific and regulatory submission documents in compliance with global regulatory standards. The role involves authoring clinical and regulatory documents, leading regulatory writing strategies for global submissions, collaborating with cross-functional product teams, mentoring junior regulatory writers, and ensuring timely delivery of high-quality documentation supporting worldwide regulatory approvals.

KEY RESPONSIBILITIES

Regulatory Writing

  • Author Clinical Study Reports (CSRs).

  • Prepare Investigator Brochures (IBs).

  • Develop Clinical Protocols and Protocol Amendments.

  • Prepare Informed Consent Forms (ICFs).

  • Author Responses to Health Authority Questions.

  • Prepare Clinical Overview Addenda.

  • Develop eCTD Module 2 Clinical Summary Documents.

  • Prepare Briefing Documents and Pediatric Investigation Plans.

  • Author Tables of All Studies and other regulatory submission documents.

Global Regulatory Submissions

  • Lead regulatory writing activities for complex global submissions.

  • Support IND, NDA, BLA, and supplemental applications.

  • Ensure submission documents meet global regulatory requirements.

  • Coordinate document preparation across product development stages.

  • Deliver submission-ready documentation within project timelines.

Cross-Functional Collaboration

  • Serve as Regulatory Writing Lead on Global Product Teams.

  • Collaborate with Global Regulatory, Safety, Clinical Development, and Evidence Generation teams.

  • Provide regulatory writing expertise during product development.

  • Contribute to Global Regulatory Plans and strategic objectives.

  • Maintain strong relationships with cross-functional stakeholders.

Document Review & Quality

  • Conduct formal review and approval of regulatory documents.

  • Ensure consistency, scientific accuracy, and regulatory compliance.

  • Apply company SOPs, guidance documents, and work instructions.

  • Maintain high-quality writing standards across all submissions.

  • Support continuous process improvement initiatives.

Leadership & Mentoring

  • Mentor and train junior regulatory writers.

  • Oversee work performed by contract and freelance medical writers.

  • Provide technical guidance on regulatory writing activities.

  • Lead departmental and cross-functional initiatives.

  • Promote best practices across the regulatory writing function.

Project Management

  • Develop and manage document timelines.

  • Coordinate multiple regulatory writing projects simultaneously.

  • Monitor project milestones and deliverables.

  • Ensure timely completion of regulatory documentation.

  • Support planning for global regulatory submissions.

Regulatory Compliance

  • Ensure compliance with ICH, GCP, and global regulatory guidelines.

  • Maintain knowledge of evolving regulatory requirements.

  • Support regulatory inspections and audits.

  • Ensure document compliance with global health authority expectations.

  • Maintain documentation within approved document management systems.

EDUCATIONAL QUALIFICATIONS

Required

One of the following:

  • Doctorate Degree with 2+ years of directly related experience.

  • Master's Degree with 6+ years of directly related experience.

  • Bachelor's Degree with 8+ years of directly related experience.

  • Associate Degree with 10+ years of directly related experience.

  • High School Diploma/GED with 12+ years of directly related experience.

Preferred

  • Advanced Degree in Life Sciences, Pharmacy, Medicine, Biotechnology, Biomedical Sciences, or a related scientific discipline.