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.
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Appleton | Kenosha | Pleasant Prairie | Portage | Waukesha |United states :
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King Abdullah Economic City | Riyadh | Rabigh | Najran | Khulais | Jeddah |Kuala Lumpur :
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Paris | Lyon |South Africa :
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