Pharmacovigilance Physician
Pharsafer Associates · Delhi · onsite · Posted 2d ago
Undisclosed0–3 yrsfulltimeSourced from
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About this role
Job Summary
The Role
Key Responsibilities
Medical Review & Case Assessment
Medical Safety Activities
Qualifications & Skills
Essential
Desirable
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.
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 ICSRs and other safety reports where required.
- 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.
Sourced from naukri
Skills
clinical trialsCROmbbsDrug safetyMedDRAclinical developmentcontinuous developmentGlobal OperationsBiotechnologyCosmeticliterature searchCommunication SkillsLiteratureBrochurescompliancemarketingLife Sciences