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Regulatory Consultant (Row Mkt Exp And Cmc – Module 3 Exp)

Syneos Health
Syneos Health
6-9 years
Not Disclosed
Remote, India, India
10 May 13, 2026
Job Description
Job Type: Full Time Hybrid Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, mRS and EQ-5D-5L., Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Regulatory Consultant (ROW Markets & CMC – Module 3 Experience)

Company: Syneos Health
Location: India – Remote
Job ID: 25108389
Experience Required: 6–9 years


Role Overview

The Regulatory Consultant will provide end-to-end regulatory support across global product development and post-approval lifecycle activities. The role focuses on ROW (Rest of World) regulatory markets, CMC Module 3 documentation, variations, and regulatory authority interactions while ensuring compliance with global regulatory standards.


Key Responsibilities

Regulatory Strategy & Submissions

  • Conduct regulatory intelligence research and gap analysis for global/regional requirements

  • Prepare and contribute to IND, NDA, MAA, PMA, CTD, and other regulatory submissions

  • Develop product development plans and regulatory strategies

  • Prepare briefing documents for Health Authority meetings and scientific advice


Post-Approval & Lifecycle Management

  • Manage post-approval variations and lifecycle maintenance activities

  • Handle API and Drug Product variations, including site transfers

  • Respond to Regulatory Authority Questions (RTQs)

  • Support regulatory maintenance across marketed products


Project Execution & Cross-Functional Support

  • Manage day-to-day regulatory deliverables within timelines and budgets

  • Work with clinical, CMC, and cross-functional global teams

  • Provide SME support for regulatory troubleshooting and issue resolution

  • Participate in multidisciplinary project teams across product lifecycle


Compliance & Quality

  • Ensure compliance with global regulatory requirements and company SOPs

  • Participate in audits and regulatory inspections support

  • Contribute to SOP development and process improvements

  • Maintain training records and complete required compliance training


Business & Client Support

  • Support proposal development and regulatory service estimates

  • Participate in client meetings and project updates

  • Contribute to regulatory training and knowledge-sharing initiatives

  • Support internal cross-functional regulatory initiatives


Required Qualifications

Education

  • Bachelor’s or PhD in Life Sciences, Pharmacy, or related scientific field

  • Or equivalent experience in regulatory/medical writing/pharmaceutical domain


Experience

  • 6–9 years in Regulatory Affairs

  • Strong experience in:

    • ROW regulatory markets

    • CMC Module 3

    • Post-approval variations

    • API & Drug Product lifecycle management

    • Site transfers

    • Regulatory submissions (IND, NDA, MAA, CTD, PMA)

    • Health Authority interactions and RTQs


Skills & Competencies

  • Strong regulatory knowledge and analytical thinking

  • Excellent written and verbal communication skills

  • Ability to work independently and in cross-functional teams

  • Strong attention to detail and quality mindset

  • Ability to manage multiple parallel regulatory projects

  • Proficiency in Microsoft Office tools

  • Strong initiative, adaptability, and problem-solving ability


Additional Requirements

  • Experience supporting global regulatory submissions

  • Ability to handle multiple project priorities simultaneously

  • Strong stakeholder and client communication skills

  • Knowledge of regulatory compliance frameworks and industry standards