Pharmacovigilance Coordinator, Benefit Risk

This is a fully remote position, open to applicants in Serbia, +2 more countries.

📋 Description

• Assist with daily pharmacovigilance and benefit-risk operations for assigned projects.

• Input and maintain project-specific information in internal systems.

• Aid in local literature reviews and related operational tasks.

• Facilitate training for affiliate staff on pertinent pharmacovigilance duties.

• Organize meetings, create agendas, and distribute meeting materials.

• Document and keep records of pharmacovigilance meeting minutes and action items.

• Oversee filing, archiving, and document management tasks.

• Provide administrative assistance to the Pharmacovigilance department and project teams.

• Help prepare and coordinate activities during audits and inspections.

• Ensure compliance with company protocols, quality standards, and client expectations.

• Participate in continuous improvement efforts and perform other assigned tasks as needed.

⛳️ Requirements

• Bachelor's or Master's degree in Pharmacy, Nursing, Life Sciences, or a related health discipline.

• Fundamental knowledge or basic understanding of Pharmacovigilance.

• Proficient in Microsoft Office Suite, including Word, Excel, and PowerPoint.

• Familiarity with databases, web-based applications, or electronic systems.

• 0–1 years of experience in pharmacovigilance, healthcare, life sciences, clinical research, or a similar field.

• Recent graduates with relevant academic backgrounds and an interest in drug safety are encouraged to apply.

🏝️ Benefits

• Remote work opportunity.

• Hybrid work arrangement encouraged for new hires living within a reasonable commute of an office, as agreed upon with the manager.

• Career advancement with a global leader in regulatory and pharmacovigilance services.

• Interaction with international pharmaceutical and biotechnology clients.

• Collaboration with seasoned professionals in drug safety and benefit-risk assessment.

• Development of knowledge in pharmacovigilance, regulatory compliance, and safety operations.

• Chance to contribute to projects that enhance patient safety and public health on a global scale.

• Equal Opportunity Employer dedicated to diversity, equity, and inclusion.

• Applications are personally assessed by a member of the recruitment team.

• Applicants will receive feedback on their application status.