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Publishing Specialist

8-10 years
Not Disclosed
10 Sept. 18, 2025
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences 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

Location: Princeton, NJ, USA
Department: Regulatory Affairs
Employment Type: Full-Time
Experience Level: Senior


Job Purpose

The Publishing Specialist is responsible for managing end-to-end regulatory publishing support for initial IND/NDA/MAA applications and life-cycle maintenance of global submissions. The role ensures high-quality, compliant, and timely regulatory submissions while supporting cross-functional teams and training initiatives.


Key Responsibilities

Regulatory Publishing & Submission Management

  • Manage publishing support for initial IND/NDA/MAA submissions and life-cycle maintenance across global regions.

  • Collaborate with cross-functional teams for planning, preparation, publishing, and quality control of regulatory submissions.

  • Develop submission-ready documents for electronic submissions, including formatting, hyperlinking, and processing MS Word and Adobe Acrobat documents.

  • Support multiple submission formats, including eCTD, NeeS/eSub, and paper submissions.

  • Troubleshoot document issues in Adobe Acrobat and MS Word; identify and address gaps with client stakeholders.

  • Manage technical aspects and provide status updates for assigned submissions.

  • Perform quality checks on published outputs to ensure zero unacceptable warnings or validation errors before submission to health authorities.

Training & Knowledge Management

  • Provide on-the-job training following a train-the-trainer model for colleagues and beginners.

  • Deliver scheduled team training to share process and health authority updates, maintaining competency across submission types.

  • Provide feedback on SOP/process improvements to enhance turnaround times and submission efficiency.

Project Coordination & Continuous Improvement

  • Support project leads in day-to-day planning and ensure timely deliverables per client expectations.

  • Coordinate effectively with cross-functional teams to receive, track, and address document gaps for efficient project execution.

  • Provide feedback to project leads on KPI trends and suggest continuous improvements in operational processes.


Desirable Skills & Experience

  • 8–10 years of experience in Regulatory Affairs.

  • Strong analytical, logical, and writing skills.

  • Hands-on experience in creating submission outputs for eCTD, NeeS, and paper submissions.

  • In-depth knowledge of US FDA and Health Canada (HC) submissions.

  • Experience managing initial IND/NDA/MAA projects and life-cycle management (LCM) submissions.

  • Ability to work under tight timelines and achieve first-time-right submissions with zero health authority rejections.

  • Proven ability to understand submission and agency requirements.

  • Effective coordination with cross-functional teams to manage and track documents.

  • Experience with tools such as: pharmaREADY®, Lorenz, Insight Publisher, Veeva Vault, eCTD Express, Extedo (advantageous).


Educational Qualifications

  • Graduate or Postgraduate degree in Life Sciences.