Remote Pharmacovigilance Specialist: Drug Safety

Placements24; Queenstown; Hybrid; NZD 90,000 - 120,000; Full time

Benefits offered by this job

Health insurance

Retirement contributions

Performance incentives

Home office setup

Flexible working hours

PV training

Job summary

Placements24 is seeking a Pharmacovigilance Specialist for a fully remote role serving global safety operations. You will collect, evaluate, and report adverse events, ensuring timely compliance with regulatory requirements and data integrity while collaborating with clinical, medical affairs, and QA teams.

The ideal candidate has a degree in Pharmacy or life sciences, at least 3 years in pharmacovigilance, strong medical terminology, and proficiency with PV databases and MS Office.

Qualifications

• Bachelor's degree in Pharmacy, Nursing, Life Sciences, or related healthcare field.
• Minimum of 3 years experience in pharmacovigilance or drug safety.
• Thorough understanding of global pharmacovigilance regulations (ICH, GVP).
• Experience with adverse event reporting systems and PV databases.
• Strong medical terminology and analytical skills.
• Excellent written and verbal communication.
• Independent worker with remote work capability.

Responsibilities

• Collect, process, and evaluate adverse event reports from various sources.
• Ensure timely and accurate reporting of safety data to regulatory agencies worldwide.
• Conduct medical assessment of adverse events and determine causality.
• Maintain and manage the pharmacovigilance database.
• Contribute to PSURs and RMPs and other safety documents.
• Liaise with internal and external stakeholders on safety matters.

Skills

Medical terminology

Analytical skills

Communication skills

Remote work

Education

Bachelor's degree in Pharmacy

Bachelor's degree in Nursing

Bachelor's degree in Life Sciences

Tools

MS Office

Job description

Placements24 is seeking a Pharmacovigilance Specialist for a fully remote role serving global safety operations. You will collect, evaluate, and report adverse events, ensuring timely compliance with regulatory requirements and data integrity while collaborating with clinical, medical affairs, and QA teams.

The ideal candidate has a degree in Pharmacy or life sciences, at least 3 years in pharmacovigilance, strong medical terminology, and proficiency with PV databases and MS Office.