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Publisher I

Novo Nordisk
4+ years
INR 8 LPA – 14 LPA
Bangalore, India
1 June 16, 2026
Job Description
Job Type: Full Time Education: M.Pharm/B.Pharm or M.Sc. Skills: CPC Certified, CPT, Data Analysis, Document Management, Life Science, Regulatory Compliance, Waterfall Model, GCP guidelines, HCPCS Level II, ICD-10-CM

Publisher I

Location: Bangalore, Karnataka, India
Employment Type: Full-Time
Company: Novo Nordisk Global Business Services (GBS)

Position Summary

The Publisher I is responsible for regulatory and clinical document publishing, electronic submission compilation, and lifecycle management support for global regulatory filings. The role ensures high-quality, compliant, and timely submission delivery while working within an integrated Clinical and Regulatory Publishing model. The position supports global regulatory strategies through eCTD publishing, document management, submission readiness, process optimization, and implementation of digital and AI-enabled publishing solutions.

Key Responsibilities

Regulatory Publishing & Submission Management

  • Prepare, compile, validate, and publish regulatory submissions.

  • Support marketing applications and lifecycle management submissions.

  • Ensure compliance with global Health Authority submission requirements.

  • Deliver electronic submissions within defined timelines and quality standards.

eCTD & Dossier Publishing

  • Compile and publish dossiers in eCTD, NeeS, and other submission formats.

  • Validate submission packages using regulatory publishing tools.

  • Ensure dossier structure complies with regional and global requirements.

  • Support submission readiness activities and publishing quality reviews.

Clinical & Regulatory Document Publishing

  • Publish clinical, non-clinical, regulatory, and safety documents.

  • Support publishing of:

    • Clinical Study Protocols

    • Clinical Study Reports (CSR)

    • Investigator Brochures (IB)

    • Regulatory Submission Documents

    • Safety Documents

  • Ensure adherence to templates, formatting standards, and submission requirements.

Document Management & Compliance

  • Maintain document quality and consistency across submissions.

  • Manage documentation within Regulatory Information Management Systems (RIMS).

  • Ensure compliance with evolving global regulatory guidelines.

  • Support inspection and audit readiness activities.

Cross-Functional Collaboration

  • Collaborate with Regulatory Affairs, Clinical Operations, Medical Writing, Safety, and Regulatory Operations teams.

  • Coordinate submission activities with global stakeholders.

  • Support integrated Clinical and Regulatory Publishing initiatives.

  • Facilitate efficient communication across project teams.

Process Improvement & Digital Innovation

  • Identify opportunities for process optimization and operational efficiency.

  • Support implementation of AI, automation, and digital publishing solutions.

  • Contribute to publishing process standardization initiatives.

  • Drive continuous improvement activities within Regulatory Operations.

Knowledge Sharing & Team Support

  • Participate in mentoring and knowledge-sharing activities.

  • Support training initiatives and best-practice development.

  • Contribute to capability building within the publishing function.

Educational Qualification

  • Bachelor's Degree in:

    • Pharmacy

    • Life Sciences

    • Biotechnology

    • Biomedical Sciences

    • Related Scientific Discipline

Preferred:

  • Master's Degree (M.Pharm, MSc, PharmD, Biotechnology, Life Sciences)

Experience Required

  • Minimum 4+ years of experience in:

    • Regulatory Operations

    • Regulatory Affairs

    • Regulatory Publishing

    • Submission Management

  • Experience with global regulatory submissions.

  • Experience in dossier compilation and electronic publishing.

  • Exposure to clinical document publishing preferred.

  • Experience with digital tools, automation, or AI-enabled publishing solutions is advantageous.