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
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