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Drug Safety Physician

2-3 years
Not Disclosed
10 June 26, 2025
Job Description
Job Type: Hybrid Education: B.Sc./M.Sc/B.Pharm/M.Pharm/Life Science 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

 

Drug Safety Physician – ICON plc | Chennai, India

Job Summary

ICON plc is seeking a Drug Safety Physician to join its global clinical research team in Chennai. This role is ideal for licensed physicians with 2–3 years of hospital-based clinical experience, looking to expand into pharmacovigilance and drug safety. You will play a pivotal role in ensuring patient safety by assessing adverse events (AEs/ADRs), supporting regulatory submissions, and delivering insights on product safety profiles. Join ICON and contribute to global drug development efforts.


Key Responsibilities

  • Conduct coding reviews (e.g., MedDRA) and assess AEs/ADRs for seriousness, expectedness, and relatedness

  • Review aggregate safety reports including PSURs, ASRs, and line listings

  • Evaluate safety signals and escalate appropriately

  • Train project teams on pharmacovigilance regulations and expedite/periodic safety reporting

  • Provide input on Project Specific Procedures and attend related meetings

  • Assist in code-break processes and safety data reviews during trials

  • Review and consult on Product Information, Company Core Data Sheets (CCDS), and other regulatory documents

  • Offer pharmacovigilance guidance for post-marketing and clinical trial reporting

  • Mentor Medical and Safety Services staff in PV practices


Required Skills & Qualifications

  • MBBS or equivalent degree with valid medical license

  • 2–3 years of clinical practice in a hospital setting

  • Strong understanding of adverse event classification and safety reporting

  • Knowledge of GCP and pharmacovigilance regulations (e.g., ICH-GCP, GVP)

  • Familiarity with MedDRA coding and safety data review processes

  • Excellent communication and analytical skills

  • Prior pharmacovigilance or clinical research experience is a plus


Perks & Benefits

  • Competitive salary package (exact amount not disclosed)

  • Annual bonus aligned with performance goals

  • Comprehensive health insurance for you and your family

  • Life assurance and retirement planning options

  • Global Employee Assistance Programme (TELUS Health)

  • Flexible benefits: gym discounts, childcare vouchers, travel subsidies, and more

  • Generous annual leave entitlements


Company Description

ICON plc is a leading global provider of healthcare intelligence and clinical research services. Serving pharmaceutical, biotech, and medical device clients across 40+ countries, ICON delivers high-impact insights and safety solutions that drive better clinical outcomes and support global drug development.


Work Mode: On-site – Chennai, India


Call-to-Action

Looking to transition into a rewarding career in drug safety and pharmacovigilance? Apply now to join ICON’s global team of healthcare innovators and help shape the future of clinical development.

Visit ICON Careers to Apply