Medical Physician Specialist I
Location: Mumbai
Job Type: Full-Time
Work Model: Remote
Job Requisition ID: 261195
Job Overview
We are seeking a highly skilled Medical Physician Specialist I to provide expert medical safety support for sponsors of pharmaceuticals, medical devices, and combination products during the post-marketing phase. This role is responsible for delivering medical review, pharmacovigilance assessment, and safety evaluation of adverse event cases while ensuring compliance with global regulatory and quality standards.
The ideal candidate will play a critical role in supporting drug safety operations, signal analysis, and aggregate review activities while maintaining excellence in medical case processing and customer service.
Experience Required
Preferred 1–2 years of clinical practice experience
Strong understanding of medical sciences, diagnosis, therapeutics, and drug treatments
Knowledge of clinical research regulatory requirements
Understanding of ICH-GCP guidelines
Experience in pharmacovigilance or drug safety case processing is advantageous
Key Responsibilities
Conduct primary medical review of adverse event and safety cases
Perform medical assessment of case seriousness, listedness/labeling, and causality
Review adverse event coding and medical narratives for accuracy and completeness
Update and maintain case-related data in safety trackers and workflow management tools
Ensure timely completion of assigned deliverables in line with quality, compliance, productivity SLAs, and KPIs
Support aggregate reporting and signal analysis activities related to single case processing
Provide medical guidance and support to pharmacovigilance/case processing teams
Deliver training to case processing team members on medical aspects of case review after one year of tenure
Maintain high standards of customer service and stakeholder support
Ensure all activities comply with internal SOPs and pharmacovigilance regulations
Required Qualifications
Bachelor’s degree in Medical Science, MD, DO, or equivalent medical qualification
Equivalent relevant experience may be considered in lieu of educational requirements
English Speaking Proficiency: ILR Level 3+ or higher
English Writing/Reading Proficiency: ILR Level 4+ or higher
Preferred Qualifications
Clinical practice background with direct patient care experience
Prior experience in pharmacovigilance, medical review, or safety surveillance preferred
Knowledge of post-marketing safety reporting requirements
Work Environment
Remote / Home-based or Office-based as determined by line manager
Why Join This Opportunity
This role offers an excellent opportunity for medical professionals seeking to expand their career in pharmacovigilance, drug safety, medical review, clinical research, and post-marketing surveillance while contributing to patient safety and regulatory excellence on a global scale.
Apply now to build your career in medical safety and pharmacovigilance.
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