Pharmacovigilance Coordinator, Case Processing (Medtech)

TL;DR

Pharmacovigilance Coordinator, Case Processing (Medtech): Monitoring and triaging communications in the PV inbox and performing data entry for clinical and post-marketing cases with an accent on safety database management and regulatory compliance. Focus on accurate case processing, PHI redaction, and ensuring high-quality distribution of safety deliverables.

Location: Must be based in Serbia (Hybrid/Remote options available)

Company

hirify.global is a global consultancy providing regulatory sciences, clinical research, and pharmacovigilance solutions to biotech and pharmaceutical organizations.

What you will do

• Manage PV mailboxes, including triage of client communications and inbound reports.
• Perform duplicate searches and initial book-in of safety cases.
• Screen and redact source documents for Protected Health Information (PHI) per company procedures.
• Execute data entry into the safety database for identifiable patients, suspect drugs, and adverse events.
• Facilitate literature-related activities and perform initial triage of regulatory authority database searches.
• Generate and distribute deliverables from the safety database in accordance with management plans.

Requirements

• Post-secondary education.
• Strong verbal, written, and interpersonal communication skills.
• Proficiency in computer use and keyboarding skills.
• Strong organization, prioritization, and attention to detail.
• Location: Must be based in Serbia.

Nice to have

• One year of industry experience.

Culture & Benefits

• Commitment to diversity, equity, and inclusion, fostering an authentic workplace.
• Flexible work arrangement supporting remote work and encouraging hybrid collaboration.
• Support for innovative, collaborative, and entrepreneurial professional spirit.
• Transparent hiring process with guaranteed application outcomes for all candidates.