Pharmacovigilance Specialist, Case Processing

🔥 4 minutes ago

🌐 United Kingdom, Serbia, +2 more countries – Remote

🇬🇧 United Kingdom – Remote 🇷🇸 Serbia – Remote 🇧🇦 Bosnia and Herzegovina – Remote 🇭🇷 Croatia – Remote

⏰ Full Time

🟢 Junior

🟡 Mid-level

🧪 Clinical Research

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This company has sponsored UK Skilled Worker visas in the past.

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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

• Process adverse event cases daily, including clinical trial and/or post-marketed cases • Code cases using MedDRA • Determine seriousness and expectedness at the event and case level • Perform case follow-up activities and identify information to collect • Create and review case narratives • Provide client notifications as required for case management • Support and contribute to training materials and training delivery • Highlight ICSR concerns and discrepancies to the Principal PV Specialist and/or Manager • Conduct peer reviews of cases for quality, consistency, and accuracy • Perform other duties as assigned

🎯 Requirements

• Bachelor's degree in life sciences required • Two years of related work experience • Strong verbal, written and interpersonal communication skills • High level of accuracy and attention to detail • Ability to identify and resolve problems in a timely manner • Ability to work independently and collaboratively in a multi-disciplinary team • Excellent organization and prioritization skills; ability to multitask • Basic knowledge of Pharmacovigilance • Up-to-date knowledge of global safety regulations for medicines • Preferred: advanced degree, RN, RPh, PharmD or equivalent

🏖️ Benefits

• Remote working supported • Hybrid working encouraged for new hires based within a reasonably short commute of an office, as agreed with the manager • Equal Opportunity Employer workplace committed to diversity, equity, and inclusion

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