Instagram
youtube
Facebook

Senior Drug Safety Physician

2-5 years
Not Disclosed
10 June 5, 2025
Job Description
Job Type: Full Time Education: MBBS, MD, PharmD, or PhD 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

 

Meta Title

Senior Drug Safety Physician – Chennai/Trivandrum

Meta Description

Apply for a Senior Drug Safety Physician role at ICON in Chennai or Trivandrum. 2–5 years of medical and PV experience. Competitive salary and benefits.

Meta Keywords

senior drug safety physician jobs, pharmacovigilance jobs India, clinical research physician Chennai, ICON careers, PV jobs Trivandrum, medical safety officer


Senior Drug Safety Physician – ICON | Chennai & Trivandrum, India

Job Summary

ICON plc is seeking a Senior Drug Safety Physician to join its Drug Safety and Pharmacovigilance division in Chennai or Trivandrum. This role is crucial in ensuring patient safety by evaluating adverse event data, overseeing regulatory reporting, and supporting clinical development projects. Ideal candidates are licensed physicians with 2 to 5 years of clinical experience and 2 to 3 years of experience in pharmacovigilance or clinical research. The role requires expertise in global safety regulations, medical assessment, and collaborative communication with cross-functional teams.


Key Responsibilities

  • Review medical coding (e.g., MedDRA) and assess adverse events for seriousness, relatedness, expectedness, and listedness

  • Evaluate aggregate safety data including patient profiles, line listings, annual reports, and periodic safety update reports (PSURs)

  • Identify and escalate safety signals emerging from clinical or post-marketing data

  • Support expedited and periodic regulatory reporting of adverse events

  • Provide input to product safety documents including Company Core Data Sheets (CCDS) and labeling

  • Participate in safety reviews, project meetings, and training initiatives

  • Contribute to the development of project-specific safety procedures and documentation

  • Guide internal teams on GVP, ICH-GCP, and global regulatory compliance


Required Skills and Qualifications

  • Medical degree (MBBS, MD, PharmD, or PhD) with a valid license

  • 2 to 5 years of clinical diagnosis and treatment experience

  • 2 to 3 years of experience in pharmacovigilance or clinical research

  • Strong understanding of ICH-GCP, GVP, MedDRA, and regulatory reporting standards

  • Proficiency in pharmacovigilance software and global PV practices

  • Excellent written and verbal communication skills

  • Ability to handle multiple priorities in a regulated, fast-paced environment


Perks and Benefits

  • Competitive base salary with performance-based bonuses

  • Comprehensive health insurance coverage for employees and dependents

  • Retirement benefits and life assurance plans

  • Paid time off and country-specific annual leave entitlements

  • Access to LifeWorks Global Employee Assistance Programme

  • Flexible benefits including wellness programs, gym discounts, and transport subsidies

  • Inclusive and diverse work environment committed to employee well-being


Company Description

ICON plc is a global leader in healthcare intelligence and clinical research services, supporting pharmaceutical, biotech, and medical device companies in advancing therapies and improving patient outcomes. With a strong presence in India and over 40 countries worldwide, ICON is committed to operational excellence and regulatory expertise in clinical development.


Work Mode

On-site – Chennai or Trivandrum Office


Call-to-Action

If you're a dedicated medical professional ready to contribute to global drug safety, apply today to join ICON's world-class pharmacovigilance team. Make a difference in patients' lives while advancing your career.

Apply Now at ThePharmaDaily.com