Regulatory Publishing Consultant

Position Summary

ProKidney is seeking a  Regulatory Publishing Consultant  to support the preparation, QC, and publishing of submission-ready regulatory documents and dossiers. This consultant will work cross-functionally with Regulatory Affairs, Medical Writing, and Quality stakeholders to ensure documents are compiled accurately, formatted to required standards, and delivered on time for submissions and internal archiving.

 

This role requires strong technical document skills, excellent attention to detail, and hands-on proficiency with the required toolset:  PerfectIt, ISI Toolbox, ESG (Electronic Submissions Gateway), Adobe Acrobat Pro, Microsoft Word, EndNote, and SharePoint .

 

Key Responsibilities (Deliverables-Focused)

Prepare submission-ready documents and components

Format and QC Word and PDF documents for submission readiness, including layout, styles, headers/footers, pagination, cross-references, and consistency checks.

Apply advanced editorial/quality tools ( PerfectIt ,  ISI Toolbox ) to improve accuracy, consistency, and compliance with agreed templates/standards.

PDF assembly and publishing support

Create and QC PDFs using  Adobe Acrobat Pro , including:

Bookmarking and hyperlinking

Document assembly/combination and file optimization

Navigation and functional QC (links/bookmarks/tables/TOCs)

File naming, version control, and readiness checks

Submission support / dispatch coordination (as applicable)

Support submission package readiness and provide required artifacts (e.g., package inventories, QC checklists).

Support dispatch activities through ESG as scoped (or coordinate with internal staff managing ESG), ensuring confirmation evidence is captured and retained.

Reference and document management

Support reference management activities in EndNote (as needed for documents requiring citations/bibliographies).

Maintain working files and deliverables within SharePoint, following folder structures, naming conventions, and document control expectations.

Cross-functional coordination

Coordinate efficiently with Regulatory Affairs, Medical Writing, and Quality contacts to obtain inputs, clarify requirements, and deliver completed outputs aligned to agreed timelines.

Communicate risks early (e.g., missing source content, formatting issues, late changes impacting timelines).

 

 

Required Qualifications

3–5 years  of experience in  Regulatory Publishing / Regulatory Operations  within biotech/pharma, CRO, or consulting environment.

Demonstrated hands-on experience producing submission-ready outputs, including advanced formatting and PDF QC.

Proficiency with:

PerfectIt

ISI Toolbox

ESG (Electronic Submissions Gateway)  (hands-on or strong familiarity, as scoped)

Adobe Acrobat Pro

Microsoft Word (advanced)

EndNote

SharePoint

Strong attention to detail, document-quality mindset, and ability to manage multiple priorities under deadline.

Ability to work independently in a remote environment with clear, proactive communication.

 

Preferred Qualifications

Experience supporting eCTD and/or non-eCTD publishing workflows (region-specific experience a plus).

Familiarity with common regulatory document standards and expectations (e.g., ICH structure awareness).

Experience working with cross-functional submission teams and tight submission timelines.

 

Deliverables / Success Measures (Examples)

On-time delivery of agreed publishing/formatting deliverables.

High first-pass quality (minimal rework due to formatting/QC issues).

Clear traceability and organization of working files in SharePoint.

Effective communication of status, risks, and completion evidence (e.g., QC checklist, dispatch confirmation where applicable).

 

Engagement Logistics

Location:  Remote

Working model: Deliverables-based; timelines and turnaround expectations agreed per project or submission plan. Hours will vary 20-40hrs/week

  ProKidney is an equal employment opportunity employer and does not discriminate against any applicant because of race, creed, color, age, national origin, ancestry, religion, gender, sexual orientation, disability, genetic information, veteran status, military status, application for military service or any other class protected by state or federal law.

Applicants must be eligible to work in the United States without the need for work visa or residency sponsorship.