Welcome Back

Google icon Sign in with Google
OR
I agree to abide by Pharmadaily Terms of Service and its Privacy Policy

Create Account

Google icon Sign up with Google
OR
By signing up, you agree to our Terms of Service and Privacy Policy
Instagram
youtube
Facebook

Drug Safety Physician

Vizen Life Sciences
Vizen Life Sciences
0-2 years
₹15 – 28 LPA
10 Aug. 21, 2025
Job Description
Job Type: Full Time Education: MBBS/MD 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

Job Title: Drug Safety Physician
Location: Hyderabad, India
Company: Vizen Life Sciences Pvt. Ltd.
Job Type: Full-Time

About the Company:
Vizen Life Sciences Pvt. Ltd. is a trusted name in pharmacovigilance and life sciences services, dedicated to ensuring global safety and compliance standards. The company focuses on delivering excellence in drug safety monitoring, regulatory support, and patient-centric solutions across pharmaceutical domains.

Role Overview:
The Drug Safety Physician will play a key role in medical review and safety evaluation, ensuring compliance with global pharmacovigilance standards for investigational and marketed products. The role involves detailed ICSR review, benefit-risk assessment of aggregate reports, and active participation in safety surveillance and client discussions.

Key Responsibilities:

  • Provide medical review, analysis, and guidance during the case handling and reporting cycle of ICSRs and ADRs.

  • Conduct detailed medical review of ICSRs to assess causality, seriousness, and completeness in line with regulations.

  • Write safety sections and contribute to benefit-risk assessments for aggregate reports (PSURs, CASRs, PADERs).

  • Provide medical guidance to Drug Safety Associates on case assessments and aggregate safety analysis.

  • Analyze ADRs during surveillance, including independent evaluation of safety risks and signal detection.

  • Participate in Safety Review Meetings and client interactions, providing medical insights and recommendations.

  • Ensure readiness and compliance during internal audits and regulatory inspections.

Education & Qualifications:

  • MBBS or MD in Pharmacology (preferred).

  • BDS candidates with relevant pharmacovigilance experience may also apply.

Skills Required:

  • Strong understanding of ICSR processes and global safety regulations.

  • Clinical research or pharmacovigilance knowledge.

  • Analytical and problem-solving ability.

  • Excellent presentation and communication skills.

  • Strong organizational and prioritization abilities.

  • Client-focused and collaborative mindset.

Why Join Us?
This role provides an excellent opportunity to lead critical aspects of drug safety, contribute to regulatory compliance, and ensure patient well-being. You will work in a collaborative environment with opportunities to apply medical expertise in global pharmacovigilance practices.

Estimated Salary: ₹15 – 28 LPA (based on seniority and experience in pharmacovigilance roles in Hyderabad).