Welcome Back

Google icon Sign in with Google
OR
I agree to abide by Pharmadaily Terms of Service and its Privacy Policy

Create Account

Google icon Sign up with Google
OR
By signing up, you agree to our Terms of Service and Privacy Policy
Instagram
youtube
Facebook

Publishing Specialist

Navitas Life Sciences
Navitas Life Sciences
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