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Document Specialist

Propharma
Propharma
3 years
Not Disclosed
Remote
10 March 21, 2026
Job Description
Job Type: Full Time Hybrid Remote Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ 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

Document Specialist – Regulatory Publishing (eCTD)

Location: India (Remote/Hybrid)
Job Type: Full-Time
Department: Regulatory Affairs / Clinical & Medical
Experience Required: Minimum 3 Years

Job Overview
We are hiring a Document Specialist with strong expertise in regulatory publishing and document formatting to support global submission activities. This role is critical in ensuring the accuracy, quality, and compliance of regulatory documents for electronic submissions (eCTD). The ideal candidate will have hands-on experience in formatting, compiling, reviewing, and publishing regulatory documents across the drug development lifecycle.

Key Responsibilities
Support electronic submission of regulatory documents including IND, CTA, NDA, BLA, and MAA through formatting, compilation, and processing
Format and review Microsoft Word documents in alignment with client style guides and global regulatory standards
Convert and validate documents into PDF format ensuring eCTD compliance, including bookmarks, hyperlinks, and metadata
Compile regulatory dossiers and reports by coordinating and assembling required documentation within timelines
Perform publishing activities for eCTD submissions, including pre- and post-publishing quality control checks
Prepare and transfer finalized documents for submission, coordinating with internal teams and clients for approvals
Ensure adherence to regulatory guidelines such as ICH E3, E6(R2), M4, EU MDR/IVDR, and company SOPs
Manage multiple publishing projects simultaneously while maintaining quality and timelines
Communicate directly with clients to manage expectations and ensure delivery accuracy
Conduct peer review and quality checks of documents prepared by team members
Stay updated with evolving regulatory publishing standards and industry best practices
Escalate issues or risks proactively to stakeholders and management
Contribute to process improvement initiatives and departmental activities

Qualifications
Bachelor’s degree in Life Sciences, Pharmacy, or related field
Minimum 3 years of experience in regulatory document publishing, formatting, or eCTD submissions
Experience in pharmaceutical, biotechnology, or CRO environments preferred

Technical Skills
Advanced proficiency in Microsoft Word (complex formatting and templates)
Strong expertise in Adobe Acrobat and regulatory publishing tools
Hands-on experience with eCTD publishing systems such as ISI Toolbox, Core Dossier, or similar platforms
Understanding of global regulatory submission standards and document structures

Core Competencies
Strong attention to detail with high accuracy in document processing
Excellent problem-solving and analytical thinking skills
Ability to manage multiple projects and meet strict deadlines
Effective communication and stakeholder management skills
Self-driven with the ability to work independently and in cross-functional teams
Proactive mindset with strong organizational and time management abilities

Work Environment
Flexible remote or hybrid working model depending on location and team requirements
Occasional flexibility in working hours may be required to support global clients

Why Join This Role
This position offers an opportunity to work on global regulatory submissions, enhance expertise in eCTD publishing, and collaborate with leading pharmaceutical and biotechnology organizations, contributing to the successful approval of innovative therapies.