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Drug Safety Physician

Naukri
Naukri
0-2 years
preferred by company
10 Dec. 22, 2025
Job Description
Job Type: Full Time 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

Drug Safety Physician – Pharmacovigilance

Company: Vizen Life Sciences
Industry: Pharmaceutical & Life Sciences
Employment Type: Full-Time, Permanent
Location: Hyderabad, Telangana, India
Experience Required: 0–2 Years
Education Required: MBBS (Any Specialization)
Openings: 1


Job Overview

Vizen Life Sciences is seeking a qualified Drug Safety Physician to support end-to-end pharmacovigilance activities for investigational and marketed products. This role involves medical review of Individual Case Safety Reports (ICSRs), aggregate safety reporting, signal detection, and regulatory compliance across global safety standards.

The ideal candidate will demonstrate strong medical judgment, foundational pharmacovigilance knowledge, and the ability to collaborate effectively with cross-functional and client-facing teams.


Key Responsibilities

  • Perform comprehensive medical review and analysis of ICSRs and ADR reports for clinical and post-marketing products

  • Assess causality, seriousness, expectedness, and completeness of safety cases in compliance with global regulatory requirements

  • Author and review safety sections and benefit–risk evaluations for aggregate reports including PSURs, CASRs, PADERs, and DSURs

  • Provide medical guidance and oversight to Drug Safety Associates for case processing and aggregate analysis

  • Conduct ongoing safety surveillance and signal detection, including independent evaluation of emerging safety risks

  • Participate in Safety Review Meetings, internal discussions, and client interactions to provide expert medical input

  • Ensure continuous audit and inspection readiness, supporting internal audits and regulatory inspections as required


Required Skills & Competencies

  • Strong knowledge of pharmacovigilance and clinical research principles

  • Thorough understanding of ICSR lifecycle management and global safety regulations

  • Hands-on experience or familiarity with Argus Safety and safety databases

  • Excellent analytical, problem-solving, and decision-making abilities

  • Strong written and verbal communication and presentation skills

  • High level of organizational, prioritization, and time-management skills

  • Client-focused mindset with attention to quality and compliance


Preferred Technical Skills

  • Pharmacovigilance

  • Drug Safety Case Processing

  • Aggregate Reporting

  • PSUR / DSUR / PADER

  • MedDRA Coding

  • Signal Detection

  • Argus Safety


Education & Experience

  • MBBS (Any specialization) from a recognized institution

  • 0–2 years of experience in Pharmacovigilance, Drug Safety, or Clinical Research

  • Fresh MBBS graduates with strong pharmacovigilance knowledge may be considered


Why Join Vizen Life Sciences

Vizen Life Sciences offers a collaborative and compliance-driven work environment where medical professionals can build a strong foundation in global drug safety operations. The organization supports continuous learning, regulatory exposure, and career growth within the pharmaceutical and life sciences domain.


Disclaimer

This job description outlines the primary responsibilities and qualifications for the role and is not intended to be an exhaustive list. Responsibilities may evolve based on business requirements and organizational needs.