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Regulatory Scientist

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ICON
4+ years
preferred by company
10 Dec. 20, 2025
Job Description
Job Type: Full Time 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

Regulatory Scientist

Location: India (Chennai, Bangalore) | Office or Remote
Employment Type: Full-Time
Industry: Clinical Research | Regulatory Affairs | CRO

Job Overview

We are seeking an experienced Regulatory Scientist to support regulatory submissions for Phase I–III clinical trials in India. This role plays a key part in ensuring regulatory compliance, submission readiness, and timely approvals in alignment with Indian regulatory requirements. The position offers the opportunity to collaborate with global pharmaceutical and biotechnology partners while contributing to the advancement of innovative therapies.

This role is ideal for regulatory professionals with hands-on experience in CDSCO submissions, SUGAM portal workflows, CTRI registrations, and Indian clinical trial regulations.


Key Responsibilities

  • Support and execute regulatory submissions for Phase I to Phase III clinical trials in India.

  • Prepare, review, and submit CT04, CT16, and related regulatory documents via the SUGAM portal.

  • Manage and ensure accurate CTRI registrations and updates.

  • Maintain regulatory documentation within TMF, CTMS, and Veeva Vault systems.

  • Ensure compliance with ICH-GCP guidelines and Indian regulatory frameworks, including NDCT Rules, 2019.

  • Collaborate with cross-functional internal teams to ensure submission readiness and milestone achievement.

  • Monitor and interpret regulatory updates, including changes in toxicity requirements and evolving CDSCO guidelines.

  • Contribute to successful regulatory outcomes through proactive planning, documentation accuracy, and effective communication.


Education and Experience Requirements

Education:

  • Bachelor’s or Master’s degree in a scientific, pharmaceutical, life sciences, or healthcare discipline.

Experience:

  • Minimum 4+ years of regulatory affairs experience, preferably within a CRO or clinical research organization.

  • Proven experience with CDSCO regulatory submission processes, including hands-on use of SUGAM and CTRI portals.

  • Working knowledge of Indian clinical trial regulations, including NDCT Rules, 2019.


Required Skills and Competencies

  • Strong understanding of ICH-GCP principles and India-specific regulatory requirements.

  • Experience working with TMF, CTMS, Veeva Vault, or similar electronic document management systems.

  • High attention to detail with the ability to manage multiple submissions and timelines.

  • Strong written and verbal communication skills.

  • Ability to collaborate effectively with cross-functional and global teams.

  • Organized, proactive, and compliance-focused approach to regulatory activities.


Work Arrangement

  • Flexible work model: Office-based or remote (home-based).

  • Full-time position supporting India-based regulatory activities with global exposure.


Why Join This Opportunity

  • Work with a globally recognized clinical research organization supporting innovative therapies.

  • Exposure to international sponsors and complex clinical development programs.

  • Competitive compensation aligned with regional benchmarks.

  • Comprehensive benefits focused on well-being, work-life balance, and long-term career growth.

  • Inclusive and collaborative work culture committed to diversity and equal opportunity.


Equal Opportunity Statement

All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, gender identity, sexual orientation, national origin, disability, or veteran status. Reasonable accommodations are available upon request.


Disclaimer

This job description outlines the general responsibilities and qualifications for this role and is not intended to be an exhaustive list. Additional duties may be assigned based on business needs.