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Regulatory Senior Consultant

Syneos Health
8+ years
₹18–28 LPA
Remote, India, India
15 July 16, 2026
Job Description
Job Type: Full Time, Hybrid, Remote Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Regulatory Affairs, Regulatory Writing, Regulatory Compliance, Global Submissions, eCTD, IND/NDA/BLA Submissions, ICH-GCP, Regulatory Strategy, Regulatory Intelligence, Labeling Strategy.

Job Title: Regulatory Senior Consultant

Company: Syneos Health

Location: Remote (India)

Employment Type: Full-time

Experience Required: 8+ years in Regulatory Affairs with expertise in CMC Module 3, Post-Approval Variations, Lifecycle Management, and EU/GCC regulatory submissions.

Education: M.Pharm (Preferred) or Master's degree in a Science-related discipline.

Salary Package: ₹18–28 LPA (Estimated as per current market standards for Regulatory Senior Consultant roles in India; exact compensation depends on experience, skills, and interview performance.)

Key Responsibilities:

  • Author and review CMC Module 3 documentation.

  • Prepare regulatory submissions for IND, NDA, MAA, PMA, CTD, and eCTD.

  • Manage Post-Approval Variations (PAV) and Lifecycle Management (LCM) activities.

  • Conduct regulatory gap analysis and product development planning.

  • Prepare regulatory agency briefing packages and support agency interactions.

  • Independently manage regulatory projects within timelines and budget.

  • Collaborate with cross-functional global teams.

  • Act as Subject Matter Expert (SME) and mentor junior team members.

  • Support proposal preparation and client interactions.

  • Ensure compliance with global regulatory guidelines and SOPs.

  • Participate in audits, quality initiatives, and process improvements.

Required Skills:

  • CMC Module 3 Authoring

  • Post-Approval Variations (PAV)

  • Lifecycle Management (LCM)

  • EU & GCC Regulatory Affairs

  • IND, NDA, MAA, PMA, CTD/eCTD Submissions

  • Regulatory Documentation & Gap Analysis

  • Microsoft Office

  • Project Management

  • Communication & Stakeholder Management

Preferred Experience:

  • Experience in EU and GCC regulatory markets.

  • Exposure to global regulatory submissions.

  • Client-facing and proposal development experience.

Work Mode: Remote

Why Join Syneos Health?

  • Global career opportunities

  • Flexible remote work

  • Learning & development programs

  • Collaborative work culture

  • Exposure to global pharmaceutical regulatory projects