Pharmacovigilance Physician

Pharsafer Associates; New Delhi; Remote; INR 900,000 - 1,300,000; Full time

Job summary

Pharsafer Associates is seeking motivated physicians to join our global Pharmacovigilance team in India. This role offers remote work, exposure to diverse safety activities, and opportunities to develop specialist expertise in clinical and post-marketing drug safety for international clients.

You will perform medical review of safety reports, contribute to risk assessments, and collaborate with cross-functional teams from a remote location to support patient safety commitments worldwide.

Qualifications

• MBBS or MD qualification.
• 0-3 years experience in Pharmacovigilance or a relevant medical role.
• Excellent written and verbal communication skills.
• Conscientious and professional approach to work.
• Proactive attitude with the ability to work on your own initiative.
• Ability to work collaboratively within a remote, cross‑functional team.
• Strong organisational skills with the ability to prioritise workload and meet timelines.
• Existing right to work in India.

Responsibilities

• Perform medical triage of safety reports.
• Undertake medical review of ICSRs and other safety reports in validated databases.
• Conduct MedDRA coding assessments and confirmations.
• Identify, approve and undertake follow-up requirements for IC…
• Perform causality assessments for reported adverse events.
• Prepare analyses of similar events (AOSEs) for SUSARs.
• Assess literature articles for safety relevance.
• Review and approve literature search strategies.
• Review safety content of Investigator Brochures.
• Prepare or approve safety sections of clinical trial protocols.
• Perform Medical Monitor responsibilities for clinical trials where required.

Skills

Medical review

Pharmacovigilance

Communication skills

Remote collaboration

Education

MBBS or MD

Job description

Job Summary

We are looking for motivated and medically qualified physicians to join our growing global Pharmacovigilance team in India. This is an excellent opportunity for early-career medical professionals looking to develop specialist expertise in clinical and post-marketing drug safety while working with international pharmaceutical, biotechnology and life sciences clients.

Working remotely as part of our collaborative global team, you’ll gain hands‑on experience across a wide range of medical safety activities, supporting the safe use of medicines and contributing to programmes that help protect patients worldwide.

The Role

As a Pharmacovigilance Physician, you will play an important role in the medical review and evaluation of Individual Case Safety Reports (ICSRs) and other safety information. Working alongside experienced Pharmacovigilance Physicians and Drug Safety professionals, you will contribute to medically sound safety assessments while ensuring compliance with global regulatory requirements.

This role offers excellent exposure to a broad range of pharmacovigilance activities and provides a strong foundation for developing a long‑term career within medical safety, with a range of responsibilities including:

Key Responsibilities

Medical Review & Case Assessment

• Perform medical triage of safety reports.
• Undertake medical review of Individual Case Safety Reports (ICSRs) and other safety reports within validated safety databases.
• Conduct MedDRA coding assessments and confirmations.
• Identify, approve and undertake follow‑up requirements for IC…
• Perform causality assessments for reported adverse events.

Medical Safety Activities

• Prepare Analyses of Similar Events (AOSEs) for applicable Suspected Unexpected Serious Adverse Reactions (SUSARs).
• Assess literature articles for safety relevance.
• Review and approve literature search strategies.
• Review the safety content of Investigator Brochures.
• Prepare or approve safety sections of clinical trial protocols.
• Perform Medical Monitor responsibilities for clinical trials where required.

Qualifications & Skills

Essential

• MBBS or MD qualification.
• 0-3 years experience in Pharmacovigilance or a relevant medical role.
• Excellent written and verbal communication skills.
• A conscientious and professional approach to work.
• A proactive attitude with the ability to work on your own initiative.
• Ability to work collaboratively within a remote, cross‑functional team.
• Strong organisational skills with the ability to prioritise workload and meet timelines.
• Existing right to work in India.

Desirable

• Understanding of clinical development and post‑marketing drug safety.
• Exposure to pharmacovigilance systems, processes or regulatory environments.

Disclaimer: This job posting and Location has been aggregated from external source. Role details, content, and availability are subject to change. Applicants are advised to confirm the latest information directly on the company website before applying.