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R&D Senior Electronic Document Specialist

Sanofi
Sanofi
3+ years
Not Disclosed
Hyderabad
10 March 17, 2026
Job Description
Job Type: Full Time 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

R&D Senior Electronic Document Specialist

Company: Sanofi
Location: Hyderabad, India
Job Type: Full-Time
Experience: Relevant experience in electronic document management (Regulatory Submissions)
Qualification: Bachelor’s Degree (Regulatory Affairs / Life Sciences / IT or related)
Salary Range: Not Specified


Job Overview

Sanofi is hiring an R&D Senior Electronic Document Specialist to support regulatory submission processes by ensuring high-quality, compliant electronic documentation.

This role focuses on preparing, formatting, validating, and managing documents for regulatory submissions (e.g., eCTD), while collaborating with cross-functional teams across R&D. The position also requires staying updated with evolving regulatory requirements and leveraging new technologies, including AI-driven tools.


Key Responsibilities

1. Document Preparation & Formatting

Create and format regulatory documents, dossiers, and reports.

Ensure adherence to templates, formatting standards, and regulatory guidelines.

Prepare submission-ready documents for regulatory filings (e.g., eCTD).


2. E-Submission Compliance

Ensure documents meet electronic submission standards (INDs, CTDs).

Maintain correct file formats, naming conventions, and metadata.

Validate submission readiness according to regulatory requirements.


3. Quality Assurance & Control

Perform detailed quality checks on documents (formatting, linking, consistency).

Identify and correct errors, inconsistencies, and compliance gaps.

Ensure accuracy and completeness of all submission documents.


4. Cross-Functional Collaboration

Work with teams across:

  • Regulatory Affairs

  • Clinical Development

  • Nonclinical/Research

  • Quality Assurance

  • CMC and IT

Collect and align required documentation for submissions.


5. Documentation & Record Management

Maintain detailed records of document preparation and revisions.

Ensure proper version control and document integrity.

Track approvals and changes throughout the lifecycle.


6. Publishing & Submission Support

Support document compilation and publishing activities.

Ensure compliance with regulatory submission standards.

Assist in final submission readiness processes.


7. Regulatory Monitoring

Stay updated with regulatory guidelines (e.g., FDA, EMA).

Track industry best practices and evolving submission requirements.

Ensure ongoing compliance with changing regulations.


8. Training & Support

Provide training to internal teams on document preparation standards.

Support teams in submission readiness and best practices.

Act as a subject matter expert in document management processes.


9. Continuous Improvement

Identify opportunities to improve document workflows and processes.

Propose and implement efficiency enhancements.

Leverage digital tools and AI to optimize document management.


Required Skills

Regulatory & Document Management

Strong knowledge of electronic submissions (eCTD, IND, CTD).

Understanding of regulatory guidelines (FDA, EMA).

Experience with document management systems (EDMS, Vault RIM).


Technical & Digital Skills

Proficiency in tools like Adobe Acrobat, MS Office.

Understanding of XML tagging, metadata, and file formats.

Ability to troubleshoot formatting and submission issues.


Quality & Attention to Detail

High attention to detail for document accuracy and compliance.

Strong quality control and review skills.

Ability to maintain consistency across large document sets.


Communication & Collaboration

Strong communication skills for cross-functional interaction.

Ability to explain technical concepts to non-technical stakeholders.

Effective teamwork and coordination skills.


Problem-Solving & Adaptability

Strong analytical and problem-solving abilities.

Ability to adapt to new technologies and regulatory changes.

Flexible approach in a dynamic R&D environment.


Preferred Qualifications

Experience in pharmaceutical regulatory submissions.

Familiarity with full drug development lifecycle documentation.

Exposure to AI-enabled document management tools.


Key Competencies

Regulatory document expertise

Electronic submission management

Quality assurance & compliance

Cross-functional collaboration

Process optimization

Attention to detail

Technical proficiency


About the Company

Sanofi is a global biopharmaceutical company focused on advancing healthcare through innovation in areas such as oncology, immunology, neurology, rare diseases, and vaccines.

Through its R&D hubs, Sanofi integrates cutting-edge science with digital technologies to accelerate drug development and deliver life-changing therapies worldwide