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Regulatory Scientist

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ICON
4 years
preferred by company
10 Jan. 14, 2026
Job Description
Job Type: Full Time Hybrid 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: Chennai, Bangalore – India
Work Model: Office-based or Home-based (Hybrid/Flexible)
Employment Type: Full-Time
Posted: 8 Days Ago
Job Requisition ID: JR137775
Company: ICON plc

About ICON plc

ICON plc is a globally recognized healthcare intelligence and clinical research organization partnering with pharmaceutical, biotechnology, and medical device companies worldwide. With a strong commitment to scientific rigor, regulatory compliance, and inclusion, ICON supports the development of innovative therapies across all phases of clinical research.

Job Summary

ICON is seeking an experienced Regulatory Scientist to support clinical trial regulatory activities in India. This role is critical in managing regulatory submissions, ensuring compliance with Indian regulatory frameworks, and supporting timely clinical trial approvals. The successful candidate will collaborate with cross-functional global teams to deliver high-quality regulatory outcomes for Phase I–III clinical studies.

Key Responsibilities

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

  • Prepare, review, and submit CT-04, CT-16, and related regulatory documents via the SUGAM portal

  • Ensure accurate and timely CTRI registrations in line with CDSCO requirements

  • Manage regulatory documentation and archiving using TMF, CTMS, and Veeva Vault systems

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

  • Collaborate with internal stakeholders across Data Integration (DI), AI, ADCI, and other functional teams to ensure submission readiness

  • Monitor and interpret regulatory updates, including evolving toxicity and safety requirements

  • Contribute to regulatory milestone planning through proactive communication and risk management

Required Qualifications and Experience

  • Bachelor’s or Master’s degree in Life Sciences, Pharmacy, Biotechnology, or a related scientific discipline

  • Minimum 4 years of experience in Regulatory Affairs, preferably within a CRO or clinical research environment

  • Strong working knowledge of CDSCO regulatory processes, including SUGAM and CTRI portals

  • Hands-on experience with TMF, CTMS, Veeva Vault, or similar electronic document management systems

  • Solid understanding of ICH-GCP and Indian clinical trial regulations (NDCT 2019)

  • Excellent attention to detail, organizational skills, and the ability to manage multiple regulatory timelines

  • Strong written and verbal communication skills for cross-functional collaboration

What ICON Offers

  • Competitive salary with country-specific benefits

  • Flexible work arrangements supporting work-life balance

  • Comprehensive health insurance coverage for employees and families

  • Retirement and long-term financial planning benefits

  • Global Employee Assistance Program (TELUS Health) with 24/7 professional support

  • Life assurance and wellness-focused initiatives

  • Structured career development and global growth opportunities

Diversity, Equity, and Inclusion

ICON is committed to fostering an inclusive, respectful, and accessible workplace. All qualified applicants will receive equal consideration for employment without discrimination based on race, gender, age, disability, religion, sexual orientation, gender identity, or any other protected characteristic. Reasonable accommodations are available throughout the hiring process.

Apply with Confidence

Candidates who may not meet every listed requirement are encouraged to apply. ICON values potential, adaptability, and a passion for regulatory science and clinical research.