Medical Physician Specialist I
Location: Mumbai, India
Job Type: Full-Time
Experience Required: 1–3 Years
Category: Clinical / Pharmacovigilance
Job ID: 261087
Overview
A rewarding opportunity is available for a Medical Physician Specialist I to contribute to post-marketing safety and pharmacovigilance activities for drugs, medical devices, and combination products. This role is ideal for medical professionals seeking to apply clinical expertise in drug safety, medical review, and regulatory compliance within a global clinical research environment.
Key Responsibilities
You will perform comprehensive medical review of individual case safety reports, including assessment of seriousness, causality, listedness, and accurate adverse event coding. The role involves reviewing and refining medical narratives to ensure clarity, accuracy, and regulatory compliance.
You will be responsible for maintaining and updating case data in tracking systems, ensuring proper documentation and workflow management. Ownership of assigned deliverables with adherence to quality standards, compliance requirements, and defined KPIs is a critical part of this role.
Additionally, you will support aggregate safety analysis and signal detection activities, contributing to overall pharmacovigilance operations. After gaining sufficient experience, you may provide training and guidance to case processing teams on medical review aspects.
The role also requires maintaining a high standard of client service and collaborating effectively with cross-functional stakeholders.
Educational Qualifications
Bachelor’s degree in Medical Sciences or a professional medical degree such as MD, DO, or equivalent.
Experience Requirements
1 to 3 years of relevant experience, including clinical practice or pharmacovigilance. Candidates with 1–2 years of clinical practice experience are strongly preferred.
Required Skills and Competencies
Strong knowledge of medical sciences, diagnosis, therapeutics, and drug treatments
Understanding of clinical research and pharmacovigilance processes
Familiarity with global regulatory requirements and ICH-GCP guidelines
Ability to perform detailed medical case assessments and narrative reviews
Excellent analytical and clinical judgment skills
Strong written and verbal communication skills in English
Ability to manage multiple deliverables with accuracy and efficiency
Work Environment
This role may be based in an office or home-based setting, depending on business requirements and manager discretion.
Why Join
This position offers an excellent pathway for medical professionals to transition into pharmacovigilance and drug safety. You will gain hands-on experience in global safety operations, regulatory frameworks, and medical review processes while contributing to patient safety and public health outcomes.
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