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Publishing Specialist

8-10 years
Not Disclosed
10 May 28, 2025
Job Description
Job Type: Full Time Remote 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: Publishing Specialist


Job Overview

We are currently seeking a Publishing Specialist to join our growing team. In this role, you will be responsible for managing end-to-end publishing support for global regulatory submissions, including initial IND/NDA/MAA filings and lifecycle maintenance submissions. You will ensure compliance with health authority requirements, work with cross-functional teams, and deliver high-quality, submission-ready output across multiple formats including eCTD, NeeS, and Paper.


Key Responsibilities

Regulatory Publishing & Submission Management

  • Manage end-to-end publishing for initial IND, NDA, MAA applications and lifecycle maintenance submissions globally

  • Format, hyperlink, and process documents in MS Word and Adobe Acrobat for electronic submission readiness

  • Troubleshoot document formatting issues and ensure alignment with submission requirements

Collaboration & Coordination

  • Coordinate with cross-functional teams to gather, track, and validate documents for timely and accurate submission

  • Collaborate on submission planning, publishing, and quality control (QC) processes

  • Provide feedback to clients and stakeholders regarding SOP improvements and documentation gaps

Compliance & Quality Control

  • Maintain current knowledge of global health authority (HA) standards, including FDA, EMA, and HC requirements

  • Perform QC checks to ensure compliance and zero critical validation errors in published submissions

  • Monitor submission health through KPI tracking and suggest improvements to project leads

Training & Process Improvement

  • Support train-the-trainer and on-the-job training for junior team members and new joiners

  • Conduct scheduled training sessions to update teams on HA requirements and process updates

  • Share submission best practices and provide feedback for continuous improvement in publishing processes


Required Experience & Qualifications

  • 8–10 years’ experience in Regulatory Affairs and submission publishing

  • Extensive hands-on experience with eCTD, NeeS, and Paper submissions

  • Demonstrated expertise in initial submissions (IND/NDA/MAA) and lifecycle management (LCM) submissions

  • Strong understanding of submission requirements from US FDA, Health Canada, and other regulatory bodies

  • Proven ability to work under tight timelines and deliver first-time-right submissions

  • High attention to detail and strong analytical/logical reasoning skills

  • Effective written communication and document review capabilities


Desirable Tools Experience

Experience with the following regulatory publishing tools is highly advantageous:

  • pharmaREADY®

  • Lorenz

  • Insight Publisher

  • Veeva Vault

  • eCTD Express

  • Extedo