Pharmacovigilance Specialist

Latinum HR Solutions; Ahmedabad District; On-site; INR 1,350,000 - 1,650,000; Full time

Job summary

Latinum HR Solutions is seeking a Medical Reviewer in Life Sciences to join our team in India. The role emphasizes pharmacovigilance (drug safety) and clinical research to ensure patient safety and regulatory compliance.

You will perform medical reviews of AE/SAE cases, evaluate data quality, support safety teams, and respond to medical queries while adhering to global standards and timelines.

Qualifications

• MBBS or MD required.
• 1–4 years of relevant experience.
• Prior experience in pharmacovigilance or clinical research preferred.

Responsibilities

• Perform medical review of AE/SAE cases, incl. literature and spontaneous reports.
• Conduct medical assessment, causality evaluation, and narrative review.
• Evaluate patient history, labs, meds for accurate case assessment.
• Support Drug Safety teams with medical expertise and data quality.
• Respond to medical queries related to ICSRs and ensure regulatory timelines.

Skills

Pharmacovigilance

Clinical Research

Medical Review

Communication

Education

MBBS or MD

Job description

Hiring : Medical Reviewer | Life Sciences

We are seeking a qualified Medical Reviewer to join our growing Life Sciences team. This opportunity is ideal for medical professionals with a strong foundation in Pharmacovigilance (Drug Safety) or Clinical Research, who are passionate about ensuring patient safety and regulatory compliance.

Eligibility Criteria

• Qualification: MBBS or MD
• Location : Mumbai/Ahmedabad/ Pune/ Bangalore
• Experience: 1 4 Years
• Budget : Upto 15 LPA (Depending on Exp)
• Prior experience in Pharmacovigilance, Drug Safety, or Clinical Research is preferred.

Key Responsibilities

• Perform comprehensive medical review of adverse event (AE/SAE) cases, including literature and spontaneous reports.
• Conduct medical assessment, causality evaluation, and review case narratives in accordance with global safety standards.Evaluate patient history, laboratory findings, concomitant medications, and clinical data for accurate case assessment.Support Drug Safety teams by providing medical expertise and ensuring high-quality safety data.Review and respond to medical queries related to Individual Case Safety Reports (ICSRs).Ensure adherence to global regulatory requirements, SOPs, and reporting timelines.Contribute to safety discussions, audits, and cross-functional collaborations.

Desired Skills

• Strong medical knowledge with an understanding of Pharmacovigilance and regulatory processes.
• Excellent analytical, problem-solving, and decision-making abilities.
• Effective communication and interpersonal skills.
• Proficiency in MS Office and the ability to work in a collaborative environment.