Pharmacovigilance Coordinator, Benefit Risk

🔥 22 hours ago

🌐 Serbia, Croatia, +1 more countries – Remote

🇷🇸 Serbia – Remote 🇭🇷 Croatia – Remote 🇲🇰 North Macedonia – Remote

⏰ Full Time

🟢 Junior

🎲 Risk

👻 Ghost score 10%

What it means: how likely this posting is sitting open without active hiring.How to read it: 60% or higher means we think this is a ghost. Lower scores are less of a worry.How we score it: age, reposts, open roles vs team size, how fast jobs close, and whether pay is listed.Fine print: an estimate from public data, not a judgment of the company. Real jobs can score high, so treat it as a hint, not a fact.

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ProPharma

WebsiteLinkedInAll Job Openings

5001 - 10000 employees

Founded 2001

🏥 Healthcare

📦 Logistics

🏭 Manufacturing

💰 $8.6M Venture Round on 2020-10

Healthcare • Logistics • Manufacturing

ProPharma is a leading research consulting organization in the life sciences industry. The company specializes in providing custom solutions across the full product lifecycle, from early discovery to post-market monitoring. ProPharma's services include regulatory sciences, clinical research solutions, quality and compliance services, pharmacovigilance, medical information, and R&D technology. Known for its deep domain expertise, ProPharma assists clients in the pharmaceuticals, biotechnology, and medical device sectors with regulatory support, clinical development, and quality management. ProPharma's global team supports a wide range of therapeutic areas including oncology, cardiovascular, and rare diseases, among others, ensuring effective and efficient delivery of life-saving therapies.

📋 Description

• Support day-to-day pharmacovigilance and benefit-risk activities across assigned projects • Enter and maintain project-related information within internal systems • Assist with local literature screening and associated operational activities • Support training of affiliate personnel on relevant pharmacovigilance responsibilities • Coordinate meetings, prepare agendas, and distribute meeting documentation • Record and maintain pharmacovigilance meeting minutes and action logs • Manage filing, archiving, and document control activities • Provide administrative support to the Pharmacovigilance department and project teams • Assist with preparation and coordination during audits and inspections • Ensure activities comply with company procedures, quality standards, and client requirements • Contribute to continuous improvement initiatives and other duties as required

🎯 Requirements

• Bachelor's or Master's degree in Pharmacy, Nursing, Life Sciences, or another health-related discipline • Basic knowledge or foundational understanding of Pharmacovigilance • Proficiency with Microsoft Office applications, including Word, Excel, and PowerPoint • Experience using databases, web-based applications, or electronic systems • 0–1 years of experience in pharmacovigilance, healthcare, life sciences, clinical research, or a related field • Recent graduates with relevant academic backgrounds and an interest in drug safety are encouraged to apply

🏖️ Benefits

• Remote opportunity • Hybrid working encouraged for new hires within a reasonably short commute of an office, as agreed with the manager • Career development in a global leader in regulatory and pharmacovigilance services • Exposure to international pharmaceutical and biotechnology clients • Collaboration with experienced drug safety and benefit-risk professionals • Development of expertise in pharmacovigilance, regulatory compliance, and safety operations • Opportunity to contribute to projects supporting patient safety and public health worldwide • Equal Opportunity Employer committed to diversity, equity, and inclusion • Applications personally reviewed by a member of the recruitment team • Applicants receive an outcome on their application