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Publishing Specialist

8-10 years
₹14 – ₹20 LPA
10 July 22, 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

Publishing Specialist – Regulatory Affairs Submissions

Location: [Not Specified]
Experience: 8–10 Years
Job Type: Full-Time


Job Overview:
We are currently seeking an experienced Publishing Specialist to support regulatory submission operations and lifecycle maintenance across global markets. This role will focus on end-to-end publishing of eCTD/NeeS/Paper submissions including formatting, hyperlinking, QC, and agency compliance. The ideal candidate should bring advanced knowledge of submission standards, regulatory tools, and agency-specific requirements such as US FDA and Health Canada (HC).


Key Responsibilities:

Submission Management:

  • Manage complete regulatory publishing lifecycle for initial IND/NDA/MAA submissions and maintenance filings globally.

  • Support eCTD, NeeS/eSub, and paper submission formats per agency specifications.

  • Coordinate with cross-functional teams to plan, prepare, publish, and QC regulatory submissions.

Document Preparation and Processing:

  • Format, hyperlink, and process documents using MS Word and Adobe Acrobat.

  • Troubleshoot document formatting issues and ensure all files meet technical requirements.

  • Identify and address submission gaps and inconsistencies in collaboration with clients and internal teams.

Quality Control and Compliance:

  • Perform quality checks on submission output and validate using agency tools ensuring no errors or rejections.

  • Ensure compliance with agency standards, guidelines, and evolving global regulatory requirements.

Collaboration and Training:

  • Train and guide team members using a train-the-trainer approach.

  • Provide feedback and SOP/process improvement suggestions to clients and leads to enhance efficiency.

  • Assist project leads in daily activity planning, tracking KPIs, and delivering on timelines.

  • Lead knowledge-sharing sessions to ensure up-to-date competency within the publishing team.


Desirable Skills and Experience:

  • 8 to 10 years of experience in Regulatory Affairs Publishing.

  • Strong analytical skills and keen attention to detail.

  • Extensive hands-on experience in submission creation for eCTD, NeeS, and paper formats.

  • Deep knowledge of US FDA and Health Canada submission requirements.

  • Proven track record with initial IND/NDA/MAA projects and lifecycle management (LCM) submissions.

  • Experience with tools like pharmaREADY®, Lorenz, Insight Publisher, Veeva Vault, eCTD Express, Extedo.

  • Excellent coordination and communication abilities to collaborate across cross-functional teams.

  • Ability to work under tight timelines and deliver first-time-right submissions with zero HA rejections.

  • Strong logical reasoning and writing capabilities.


Estimated Salary: ₹14 – ₹20 LPA (based on experience and tool proficiency)