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Medical Reviewer – Vaf 192, 193, 194

2-4 years
Not Disclosed
10 March 26, 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

Medical Reviewer – VAF 192, 193, 194
Location: India (Remote Possible)
Category: Safety and Vigilance, Life Cycle
Contract Type: Permanent

Company Overview:
ProductLife Group (PLG) is dedicated to improving human health by providing regulatory compliance services to ensure the safe and effective use of medical solutions. PLG supports clients throughout the product life cycle, offering consulting and outsourcing services in regulatory affairs, quality and compliance, vigilance, and medical information across 130+ countries.

Key Responsibilities:

Medical Review and Assessment:

  • Conduct medical reviews of ICSRs (Spontaneous, literature, clinical studies).

  • Support in seriousness assessment and initial triage of cases.

  • Evaluate causality, medical assessment, and benefit-risk of medicinal products.

  • Perform additional case reviews to ensure accuracy and competency.

Regulatory Compliance and Oversight:

  • Ensure compliance with client conventions and expectations.

  • Participate in audits and inspections as required.

  • Understand client needs and deliver results that exceed expectations.

Training and Mentoring:

  • Mentor and train other team members on good assessment practices and MedDRA coding.

  • Provide constructive feedback and support continuous improvement.

Client Communication and Reporting:

  • Engage in client communications to ensure alignment on requirements.

  • Address queries and provide clarifications as needed.

Candidate Requirements:

Education:

  • MBBS or MD (Doctor of Medicine)

Experience:

  • Minimum 2-4 years of experience in pharmacovigilance, working with service providers or pharmaceutical companies.

  • Experience with safety databases and client communications.

Additional Skills:

  • Effective written and verbal communication skills to explain complex concepts.

  • Clinical experience is an advantage.

  • Strong analytical skills with attention to detail.

  • Emotional intelligence and adaptability.

  • Ability to deliver constructive feedback.

  • Reliable, punctual, and well-organized.

  • Flexibility to adapt to changing project requirements.